montreal_children_s

Montreal Children's Hospital is a children's hospital in Montreal, Quebec, Canada. Founded in 1904, it is affiliated with the McGill University Health Centre and McGill University, Faculty of Medicine. The hospital has 154 single-patient rooms, 52-bed neonatology unit, 6 operating rooms and 6 intervention rooms.

1: Cunan ET, Dudley RWR, Shemie SD. In reply: Withholding therapeutic interventions in brain(stem) death: is it a self-fulfilling prophecy? Can J Anaesth. 2022 Sep 12. doi: 10.1007/s12630-022-02326-w. Epub ahead of print. PMID: 36097131.

2: Marefi A, Husein N, Dunbar M, Dewey D, Letourneau N, Oskoui M, Kirton A, Shevell MI; Canadian Cerebral Palsy Registry (CCPR). Risk Factors for Term-Born Periventricular White Matter Injury in Children With Cerebral Palsy: A Case- Control Study. Neurology. 2022 Aug 30:10.1212/WNL.0000000000201274. doi: 10.1212/WNL.0000000000201274. Epub ahead of print. PMID: 36041870.

3: Ashour M, Minato E, Alawadhi A, Berrahmoune S, Simard-Tremblay E, Poulin C, Myers KA. Diagnostic utility of specific abnormal EEG patterns in children for determining epilepsy phenotype and presence of structural brain abnormalities. Heliyon. 2022 Aug 10;8(8):e10172. doi: 10.1016/j.heliyon.2022.e10172. PMID: 36033323; PMCID: PMC9399955.

4: Eising E, Mirza-Schreiber N, de Zeeuw EL, Wang CA, Truong DT, Allegrini AG, Shapland CY, Zhu G, Wigg KG, Gerritse ML, Molz B, Alagöz G, Gialluisi A, Abbondanza F, Rimfeld K, van Donkelaar M, Liao Z, Jansen PR, Andlauer TFM, Bates TC, Bernard M, Blokland K, Bonte M, Børglum AD, Bourgeron T, Brandeis D, Ceroni F, Csépe V, Dale PS, de Jong PF, DeFries JC, Démonet JF, Demontis D, Feng Y, Gordon SD, Guger SL, Hayiou-Thomas ME, Hernández-Cabrera JA, Hottenga JJ, Hulme C, Kere J, Kerr EN, Koomar T, Landerl K, Leonard GT, Lovett MW, Lyytinen H, Martin NG, Martinelli A, Maurer U, Michaelson JJ, Moll K, Monaco AP, Morgan AT, Nöthen MM, Pausova Z, Pennell CE, Pennington BF, Price KM, Rajagopal VM, Ramus F, Richer L, Simpson NH, Smith SD, Snowling MJ, Stein J, Strug LJ, Talcott JB, Tiemeier H, van der Schroeff MP, Verhoef E, Watkins KE, Wilkinson M, Wright MJ, Barr CL, Boomsma DI, Carreiras M, Franken MJ, Gruen JR, Luciano M, Müller-Myhsok B, Newbury DF, Olson RK, Paracchini S, Paus T, Plomin R, Reilly S, Schulte-Körne G, Tomblin JB, van Bergen E, Whitehouse AJO, Willcutt EG, St Pourcain B, Francks C, Fisher SE. Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Proc Natl Acad Sci U S A. 2022 Aug 30;119(35):e2202764119. doi: 10.1073/pnas.2202764119. Epub 2022 Aug 23. PMID: 35998220; PMCID: PMC9436320.

5: Jia X, Zhang S, Tan S, Du B, He M, Qin H, Chen J, Duan X, Luo J, Chen F, Ouyang L, Wang J, Chen G, Yu B, Zhang G, Zhang Z, Lyu Y, Huang Y, Jiao J, Chen JYH, Swoboda KJ, Agolini E, Novelli A, Leoni C, Zampino G, Cappuccio G, Brunetti-Pierri N, Gerard B, Ginglinger E, Richer J, McMillan H, White-Brown A, Hoekzema K, Bernier RA, Kurtz-Nelson EC, Earl RK, Meddens C, Alders M, Fuchs M, Caumes R, Brunelle P, Smol T, Kuehl R, Day-Salvatore DL, Monaghan KG, Morrow MM, Eichler EE, Hu Z, Yuan L, Tan J, Xia K, Shen Y, Guo H. De novo variants in genes regulating stress granule assembly associate with neurodevelopmental disorders. Sci Adv. 2022 Aug 19;8(33):eabo7112. doi: 10.1126/sciadv.abo7112. Epub 2022 Aug 17. PMID: 35977029; PMCID: PMC9385150.

6: Hatoum R, Chen JS, Lavergne P, Shlobin NA, Wang A, Elkaim LM, Dodin P, Couturier CP, Ibrahim GM, Fallah A, Venne D, Perreault S, Wang AC, Jabado N, Dudley RWR, Weil AG. Extent of Tumor Resection and Survival in Pediatric Patients With High-Grade Gliomas: A Systematic Review and Meta-analysis. JAMA Netw Open. 2022 Aug 1;5(8):e2226551. doi: 10.1001/jamanetworkopen.2022.26551. PMID: 35972743; PMCID: PMC9382445.

7: Botelho F, Gripp K, Yanchar N, Naus A, Poenaru D, Baird R, Reis E, Farias L, Silva AG, Viana F, Neto JAP, Silva S, Ribeiro K, Gatto L, Faleiro MD, Fernandez MG, Salgado LS, Sampaio NZ, Faleiro MD, Mendes AL, Ferreira RV, Marcião L, Canto G, Borges J, Araújo V, Andrade G, Braga J, Bentes L, Pinto L, Ndasi HT, Amlani LM, Aminake G, Penda X, Tima S, Lechtig A, Agarwal-Harding KJ, Whyte M, Fowler- Woods M, Fowler-Woods A, Shingoose G, Hatala A, Daeninck F, Vergis A, Clouston K, Hardy K, Djadje L, Djoutsop OM, Djabo AT, Kanmounye US, Youmbi VN, Kakobo P, Djoutsop OM, Djabo AT, Kanmounye US, Tafesse S, Tamene B, Chimdesa Z, Alemayehu E, Abera B, Yifru D, Belachew FK, Tirsit A, Deyassa N, Moen BE, Sundstrøm T, Lund-Johansen M, Abebe M, Khan R, Mekasha A, Soklaridis S, Haji F, Asingei J, O'Flynn EP, O'Donovan DT, Masuka SC, Mashava D, Akello FV, Ulisubisya MM, Franco H, Njai A, Simister S, Joseph M, Woolley P, James D, Evans FM, Rai E, Roy N, Bansal V, Kamble J, Aroke A, David S, Veetil D, Soni KD, Wärnberg MG, Zadey S, Vissoci JRN, Iyer H, Zadey S, Shetty R, Zadey S, Jindal A, Iyer H, Ouma G, Shah SSNH, Hinchman C, Rayel IM, Dworkin M, Agarwal-Harding KJ, Mlinde E, Amlani LM, May CJ, Banza LN, Chokotho L, Agarwal-Harding KJ, Dworkin M, Mbomuwa F, Chidothi P, Martin C Jr, Harrison WJ, Agarwal-Harding KJ, Chokotho L, Paek S, Amlani L, Mbomuwa F, Chidothi P, Martin C Jr, Harrison WJ, Agarwal-Harding KJ, Chokotho L, Adégné T, Abdoulmouinou P, Amadou T, Youssouf T, Madiassa K, Younoussa DM, Moussa S, Amadou B, Hawa T, Laurent A, Jesuyajolu DA, Okeke CA, Obuh O, Jesuyajolu DA, Ehizibue PE, Ikemefula NE, Ekennia-Ebeh JO, Ibraham AA, Ikegwuonu OE, Diehl TM, Bunogerane GJ, Neal D, Ndibanje AJ, Petroze RT, Ntaganda E, Milligan L, Cairncross L, Malherbe F, Roodt L, Kyengera DK, O'Hara NN, Stockton D, Bedada A, Hsiao M, Chilisa U, Yarranton B, Chinyepi N, Azzie G, Moon J, Rehany Z, Bakhshi M, Bergeron A, Boulanger N, Watt L, Wong EG, Pawlak N, Bierema C, Ameh E, Bekele A, Jimenez MF, Lakhoo K, Roy N, Sacato H, Tefera G, Ozgediz D, Jayaraman S, Peric I, Youngson G, Ameh E, Borgstein E, O'Flynn E; CROCODILE study group, Simoes J, Kingsley PA, Sasson L, Dekel H, Sternfeld AR, Assa S, Sarid RS, Mnong'one NJ, Sharau GG, Mongella SM, Caryl WG, Goldman B, Bola R, Ngonzi J, Ujoh F, Kihumuro RB, Lett R, Torquato A, Tavares C, Lech G, Džunic A, Ujoh F, Gusa V, Apeaii R, Noor R, Bola R, Guyan IO, Christilaw J, Hodgins S, Lett R, Binda C, Heo K, Cheng S, Foggin H, Hu G, Lam S, Feng L, Labinaz A, Adams J, Livergant R, Williams S, Vasanthakumaran T, Lounes Y, Mata J, Hache P, Schamberg-Bahadori C, Monytuil A, Mayom E, Joharifard S, Joos É, Paterson A, Maswime S, Hardy A, Pearse RM, Biccard BM; African Surgical Outcomes (ASOS) group and International Surgical Outcomes (ISOS) group, Salehi M, Zivkovic I, Jatana S, Joharifard S, Joos É, Flores MJ, Brown KE, Roberts HJ, Donnelley CA, von Kaeppler EP, Eliezer E, Haonga B, Morshed S, Shearer DW. Decolonizing Global Surgery: Bethune Round Table, 2022 Conference on Global Surgery (virtual), June 16-18, 2022. Can J Surg. 2022 Aug 12;65(4 Suppl 1):S1-S18. doi: 10.1503/cjs.007622. PMID: 35961679; PMCID: PMC9388215.

8: Bolduc ME, Rennick JE, Gagnon I, Sokol E, Brossard-Racine M, Majnemer A. Identifying developmental challenges of youth with congenital heart defects: A patient-oriented perspective. Child Care Health Dev. 2022 Aug 9. doi: 10.1111/cch.13037. Epub ahead of print. PMID: 35945137.

9: Pekeles H, Myers KA. Post-vaccination drug-resistant epileptic spasms associated with homozygous IFNAR2 pathogenic variant: Case report^✰. Seizure. 2022 Jul 26;101:117-119. doi: 10.1016/j.seizure.2022.07.016. Epub ahead of print. PMID: 35944424.

10: Sahly AN, Buhas D, Myers KA. MT-TA pathogenic variants may cause developmental and epileptic encephalopathy without myopathy. Am J Med Genet A. 2022 Aug 3. doi: 10.1002/ajmg.a.62925. Epub ahead of print. PMID: 35920329.

11: Nolden KA, Egner JM, Collier JJ, Russell OM, Alston CL, Harwig MC, Widlansky ME, Sasorith S, Barbosa IA, Douglas AG, Baptista J, Walker M, Donnelly DE, Morris AA, Tan HJ, Kurian MA, Gorman K, Mordekar S, Deshpande C, Samanta R, McFarland R, Hill RB, Taylor RW, Oláhová M. Novel DNM1L variants impair mitochondrial dynamics through divergent mechanisms. Life Sci Alliance. 2022 Aug 1;5(12):e202101284. doi: 10.26508/lsa.202101284. PMID: 35914810; PMCID: PMC9354038.

12: Rasulo FA, Hopkins P, Lobo FA, Pandin P, Matta B, Carozzi C, Romagnoli S, Absalom A, Badenes R, Bleck T, Caricato A, Claassen J, Denault A, Honorato C, Motta S, Meyfroidt G, Radtke FM, Ricci Z, Robba C, Taccone FS, Vespa P, Nardiello I, Lamperti M. Processed Electroencephalogram-Based Monitoring to Guide Sedation in Critically Ill Adult Patients: Recommendations from an International Expert Panel-Based Consensus. Neurocrit Care. 2022 Jul 27. doi: 10.1007/s12028-022-01565-5. Epub ahead of print. PMID: 35896766.

13: Larivière S, Royer J, Rodríguez-Cruces R, Paquola C, Caligiuri ME, Gambardella A, Concha L, Keller SS, Cendes F, Yasuda CL, Bonilha L, Gleichgerrcht E, Focke NK, Domin M, von Podewills F, Langner S, Rummel C, Wiest R, Martin P, Kotikalapudi R, O'Brien TJ, Sinclair B, Vivash L, Desmond PM, Lui E, Vaudano AE, Meletti S, Tondelli M, Alhusaini S, Doherty CP, Cavalleri GL, Delanty N, Kälviäinen R, Jackson GD, Kowalczyk M, Mascalchi M, Semmelroch M, Thomas RH, Soltanian-Zadeh H, Davoodi-Bojd E, Zhang J, Winston GP, Griffin A, Singh A, Tiwari VK, Kreilkamp BAK, Lenge M, Guerrini R, Hamandi K, Foley S, Rüber T, Weber B, Depondt C, Absil J, Carr SJA, Abela E, Richardson MP, Devinsky O, Severino M, Striano P, Tortora D, Kaestner E, Hatton SN, Vos SB, Caciagli L, Duncan JS, Whelan CD, Thompson PM, Sisodiya SM, Bernasconi A, Labate A, McDonald CR, Bernasconi N, Bernhardt BC. Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expression. Nat Commun. 2022 Jul 27;13(1):4320. doi: 10.1038/s41467-022-31730-5. PMID: 35896547; PMCID: PMC9329287.

14: Markati T, Oskoui M, Farrar MA, Duong T, Goemans N, Servais L. Emerging therapies for Duchenne muscular dystrophy. Lancet Neurol. 2022 Sep;21(9):814-829. doi: 10.1016/S1474-4422(22)00125-9. Epub 2022 Jul 15. PMID: 35850122.

15: Tsai JW, Cejas P, Wang DK, Patel S, Wu DW, Arounleut P, Wei X, Zhou N, Syamala S, Dubois FPB, Crane A, Pelton K, Vogelzang J, Sousa C, Baguette A, Chen X, Condurat AL, Dixon-Clarke SE, Zhou KN, Lu SD, Gonzalez EM, Chacon MS, Digiacomo JJ, Kumbhani R, Novikov D, Hunter J, Tsoli M, Ziegler DS, Dirksen U, Jager N, Balasubramanian GP, Kramm CM, Nathrath M, Bielack S, Baker SJ, Zhang J, McFarland JM, Getz G, Aguet F, Jabado N, Witt O, Pfister SM, Ligon KL, Hovestadt V, Kleinman CL, Long H, Jones DTW, Bandopadhayay P, Phoenix TN. FOXR2 Is an Epigenetically Regulated Pan-Cancer Oncogene That Activates ETS Transcriptional Circuits. Cancer Res. 2022 Sep 2;82(17):2980-3001. doi: 10.1158/0008-5472.CAN-22-0671. PMID: 35802025.

16: Dubois FPB, Shapira O, Greenwald NF, Zack T, Wala J, Tsai JW, Crane A, Baguette A, Hadjadj D, Harutyunyan AS, Kumar KH, Blattner-Johnson M, Vogelzang J, Sousa C, Kang KS, Sinai C, Wang DK, Khadka P, Lewis K, Nguyen L, Malkin H, Ho P, O'Rourke R, Zhang S, Gold R, Deng D, Serrano J, Snuderl M, Jones C, Wright KD, Chi SN, Grill J, Kleinman CL, Goumnerova LC, Jabado N, Jones DTW, Kieran MW, Ligon KL, Beroukhim R, Bandopadhayay P. Structural variants shape driver combinations and outcomes in pediatric high-grade glioma. Nat Cancer. 2022 Aug;3(8):994-1011. doi: 10.1038/s43018-022-00403-z. Epub 2022 Jul 4. PMID: 35788723.

17: Srivastava R, Dunbar M, Shevell M, Oskoui M, Basu A, Rivkin MJ, Shany E, de Vries LS, Dewey D, Letourneau N, Hill MD, Kirton A. Development and Validation of a Prediction Model for Perinatal Arterial Ischemic Stroke in Term Neonates. JAMA Netw Open. 2022 Jun 1;5(6):e2219203. doi: 10.1001/jamanetworkopen.2022.19203. PMID: 35767262; PMCID: PMC9244611.

18: Mirchi A, Richer J, Oskoui M, McMillan HJ. NTRK1-related Hereditary Sensory and Autonomic Neuropathy Type 4: The Role of the Histamine Challenge Test. Child Neurol Open. 2022 Jun 20;9:2329048×221108826. doi: 10.1177/2329048×221108826. PMID: 35756968; PMCID: PMC9218906.

19: Bainbridge MN, Mazumder A, Ogasawara D, Abou Jamra R, Bernard G, Bertini E, Burglen L, Cope H, Crawford A, Derksen A, Dure L, Gantz E, Koch-Hogrebe M, Hurst ACE, Mahida S, Marshall P, Micalizzi A, Novelli A, Peng H, Rodriguez D, Robbins SL, Rutledge SL, Scalise R, Schließke S, Shashi V, Srivastava S, Thiffault I, Topol S; Undiagnosed Disease Network, Qebibo L, Wieczorek D, Cravatt B, Haricharan S, Torkamani A, Friedman J. Endocannabinoid dysfunction in neurological disease: neuro-ocular DAGLA-related syndrome (NODRS). Brain. 2022 Jun 23:awac223. doi: 10.1093/brain/awac223. Epub ahead of print. PMID: 35737950.

20: Yaqubi M, Luo JXX, Baig S, Cui QL, Petrecca K, Desu H, Larochelle C, Afanasiev E, Hall JA, Dudley R, Srour M, Haglund L, Ouellet J, Georgiopoulos M, Santaguida C, Sonnen JA, Healy LM, Stratton JA, Kennedy TE, Antel JP. Regional and age-related diversity of human mature oligodendrocytes. Glia. 2022 Oct;70(10):1938-1949. doi: 10.1002/glia.24230. Epub 2022 Jun 23. PMID: 35735919.

21: Strauss KA, Farrar MA, Muntoni F, Saito K, Mendell JR, Servais L, McMillan HJ, Finkel RS, Swoboda KJ, Kwon JM, Zaidman CM, Chiriboga CA, Iannaccone ST, Krueger JM, Parsons JA, Shieh PB, Kavanagh S, Wigderson M, Tauscher-Wisniewski S, McGill BE, Macek TA. Onasemnogene abeparvovec for presymptomatic infants with three copies of SMN2 at risk for spinal muscular atrophy: the Phase III SPR1NT trial. Nat Med. 2022 Jul;28(7):1390-1397. doi: 10.1038/s41591-022-01867-3. Epub 2022 Jun 17. PMID: 35715567; PMCID: PMC9205287.

22: Strauss KA, Farrar MA, Muntoni F, Saito K, Mendell JR, Servais L, McMillan HJ, Finkel RS, Swoboda KJ, Kwon JM, Zaidman CM, Chiriboga CA, Iannaccone ST, Krueger JM, Parsons JA, Shieh PB, Kavanagh S, Tauscher-Wisniewski S, McGill BE, Macek TA. Onasemnogene abeparvovec for presymptomatic infants with two copies of SMN2 at risk for spinal muscular atrophy type 1: the Phase III SPR1NT trial. Nat Med. 2022 Jul;28(7):1381-1389. doi: 10.1038/s41591-022-01866-4. Epub 2022 Jun 17. PMID: 35715566; PMCID: PMC9205281.

23: Severino M, Tortora D, Reid C, Uccella S, Nobili L, Accogli A, Srour M, Ramaglia A, Sudhakar S, Consales A, Pavanello M, Piatelli G, James G, Ravegnani M, Rossi A, Mankad K. Imaging characteristics and neurosurgical outcome in subjects with agenesis of the corpus callosum and interhemispheric cysts. Neuroradiology. 2022 Jun 7. doi: 10.1007/s00234-022-02990-1. Epub ahead of print. PMID: 35670822.

24: Hermans D, Houben E, Baeten P, Slaets H, Janssens K, Hoeks C, Hosseinkhani B, Duran G, Bormans S, Gowing E, Hoornaert C, Beckers L, Fung WK, Schroten H, Ishikawa H, Fraussen J, Thoelen R, de Vries HE, Kooij G, Zandee S, Prat A, Hellings N, Broux B. Oncostatin M triggers brain inflammation by compromising blood-brain barrier integrity. Acta Neuropathol. 2022 Aug;144(2):259-281. doi: 10.1007/s00401-022-02445-0. Epub 2022 Jun 6. PMID: 35666306.

25: Yossofzai O, Fallah A, Maniquis C, Wang S, Ragheb J, Weil AG, Brunette- Clement T, Andrade A, Ibrahim GM, Mitsakakis N, Widjaja E. Development and validation of machine learning models for prediction of seizure outcome after pediatric epilepsy surgery. Epilepsia. 2022 Aug;63(8):1956-1969. doi: 10.1111/epi.17320. Epub 2022 Jun 25. PMID: 35661152.

26: Lopez SM, Aksman LM, Oxtoby NP, Vos SB, Rao J, Kaestner E, Alhusaini S, Alvim M, Bender B, Bernasconi A, Bernasconi N, Bernhardt B, Bonilha L, Caciagli L, Caldairou B, Caligiuri ME, Calvet A, Cendes F, Concha L, Conde-Blanco E, Davoodi-Bojd E, de Bézenac C, Delanty N, Desmond PM, Devinsky O, Domin M, Duncan JS, Focke NK, Foley S, Fortunato F, Galovic M, Gambardella A, Gleichgerrcht E, Guerrini R, Hamandi K, Ives-Deliperi V, Jackson GD, Jahanshad N, Keller SS, Kochunov P, Kotikalapudi R, Kreilkamp BAK, Labate A, Larivière S, Lenge M, Lui E, Malpas C, Martin P, Mascalchi M, Medland SE, Meletti S, Morita-Sherman ME, Owen TW, Richardson M, Riva A, Rüber T, Sinclair B, Soltanian-Zadeh H, Stein DJ, Striano P, Taylor PN, Thomopoulos SI, Thompson PM, Tondelli M, Vaudano AE, Vivash L, Wang Y, Weber B, Whelan CD, Wiest R, Winston GP, Yasuda CL, McDonald CR, Alexander DC, Sisodiya SM, Altmann A; ENIGMA-Epilepsy Working Group. Event- based modeling in temporal lobe epilepsy demonstrates progressive atrophy from cross-sectional data. Epilepsia. 2022 Aug;63(8):2081-2095. doi: 10.1111/epi.17316. Epub 2022 Jun 25. PMID: 35656586.

27: Paul F, Ng C, Sahari UBM, Nafissi S, Nilipoor Y, Tavasoli AR, Bonnard C, Wong PM, Nabavizadeh N, Altunoğlu U, Estiar MA, Majoie CB, Lee H, Nelson SF, Gan-Or Z, Rouleau GA, Van Veldhoven PP, Massie R, Hennekam RC, Kariminejad A, Reversade B. RABENOSYN separation-of-function mutations uncouple endosomal recycling from lysosomal degradation, causing a distinct Mendelian Disorder. Hum Mol Genet. 2022 Jun 2:ddac120. doi: 10.1093/hmg/ddac120. Epub ahead of print. PMID: 35652444.

28: Marchi M, Elkrief L, Alkema A, van Gastel W, Schubart CD, van Eijk KR, Luykx JJ, Branje S, Mastrotheodoros S, Galeazzi GM, van Os J, Cecil CA, Conrod PJ, Boks MP. Childhood maltreatment mediates the effect of the genetic background on psychosis risk in young adults. Transl Psychiatry. 2022 Jun 1;12(1):219. doi: 10.1038/s41398-022-01975-1. PMID: 35650188; PMCID: PMC9160238.

29: Bong CL, Ho D, Allen JC, Lim GS, Tan HK, Broekman BFP, Fabila T, Reddy S, Koh WP, Swee-Kim Tan J, Meaney M, Rifkin-Graboi A. Early Neurodevelopmental Outcomes Following Exposure to General Anesthesia in Infancy: EGAIN, a Prospective Cohort Study. J Neurosurg Anesthesiol. 2022 May 26. doi: 10.1097/ANA.0000000000000857. Epub ahead of print. PMID: 35613046.

30: Wong C, Barkai O, Wang F, Perez CT, Lev S, Cai W, Tansley S, Yousefpour N, Hooshmandi M, Lister KC, Latif M, Cuello AC, Prager-Khoutorsky M, Mogil JS, Séguéla P, De Koninck Y, Ribeiro-da-Silva A, Binshtok AM, Khoutorsky A. mTORC2 mediates structural plasticity in distal nociceptive endings that contributes to pain hypersensitivity following inflammation. J Clin Invest. 2022 Aug 1;132(15):e152635. doi: 10.1172/JCI152635. PMID: 35579957; PMCID: PMC9337825.

31: Guberman GI, Stojanovski S, Nishat E, Ptito A, Bzdok D, Wheeler AL, Descoteaux M. Multi-tract multi-symptom relationships in pediatric concussion. Elife. 2022 May 17;11:e70450. doi: 10.7554/eLife.70450. PMID: 35579325; PMCID: PMC9132577.

32: Manry J, Bastard P, Gervais A, Le Voyer T, Rosain J, Philippot Q, Michailidis E, Hoffmann HH, Eto S, Garcia-Prat M, Bizien L, Parra-Martínez A, Yang R, Haljasmägi L, Migaud M, Särekannu K, Maslovskaja J, de Prost N, Tandjaoui-Lambiotte Y, Luyt CE, Amador-Borrero B, Gaudet A, Poissy J, Morel P, Richard P, Cognasse F, Troya J, Trouillet-Assant S, Belot A, Saker K, Garçon P, Rivière JG, Lagier JC, Gentile S, Rosen LB, Shaw E, Morio T, Tanaka J, Dalmau D, Tharaux PL, Sene D, Stepanian A, Mégarbane B, Triantafyllia V, Fekkar A, Heath JR, Franco JL, Anaya JM, Solé-Violán J, Imberti L, Biondi A, Bonfanti P, Castagnoli R, Delmonte OM, Zhang Y, Snow AL, Holland SM, Biggs CM, Moncada-Vélez M, Arias AA, Lorenzo L, Boucherit S, Anglicheau D, Planas AM, Haerynck F, Duvlis S, Ozcelik T, Keles S, Bousfiha AA, El Bakkouri J, Ramirez-Santana C, Paul S, Pan-Hammarström Q, Hammarström L, Dupont A, Kurolap A, Metz CN, Aiuti A, Casari G, Lampasona V, Ciceri F, Barreiros LA, Dominguez-Garrido E, Vidigal M, Zatz M, van de Beek D, Sahanic S, Tancevski I, Stepanovskyy Y, Boyarchuk O, Nukui Y, Tsumura M, Vidaur L, Tangye SG, Burrel S, Duffy D, Quintana-Murci L, Klocperk A, Kann NY, Shcherbina A, Lau YL, Leung D, Coulongeat M, Marlet J, Koning R, Reyes LF, Chauvineau-Grenier A, Venet F, Monneret G, Nussenzweig MC, Arrestier R, Boudhabhay I, Baris-Feldman H, Hagin D, Wauters J, Meyts I, Dyer AH, Kennelly SP, Bourke NM, Halwani R, Sharif-Askari FS, Dorgham K, Sallette J, Sedkaoui SM, AlKhater S, Rigo-Bonnin R, Morandeira F, Roussel L, Vinh DC, Erikstrup C, Condino-Neto A, Prando C, Bondarenko A, Spaan AN, Gilardin L, Fellay J, Lyonnet S, Bilguvar K, Lifton RP, Mane S; HGID Lab; COVID Clinicians; COVID-STORM Clinicians; NIAID Immune Response to COVID Group; NH-COVAIR Study Group; Danish CHGE; Danish Blood Donor Study; St. James's Hospital, SARS CoV2 Interest Group; French COVID Cohort Study Group; Imagine COVID-Group; Milieu Intérieur Consortium; CoV-Contact Cohort; Amsterdam UMC Covid-19 Biobank Investigators; COVID Human Genetic Effort; CP-COVID-19 Group; CONSTANCES cohort; 3C-Dijon Study; Cerba Health-Care; Etablissement Français du Sang Study group, Anderson MS, Boisson B, Béziat V, Zhang SY, Andreakos E, Hermine O, Pujol A, Peterson P, Mogensen TH, Rowen L, Mond J, Debette S, de Lamballerie X, Burdet C, Bouadma L, Zins M, Soler-Palacin P, Colobran R, Gorochov G, Solanich X, Susen S, Martinez- Picado J, Raoult D, Vasse M, Gregersen PK, Piemonti L, Rodríguez-Gallego C, Notarangelo LD, Su HC, Kisand K, Okada S, Puel A, Jouanguy E, Rice CM, Tiberghien P, Zhang Q, Casanova JL, Abel L, Cobat A. The risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies. Proc Natl Acad Sci U S A. 2022 May 24;119(21):e2200413119. doi: 10.1073/pnas.2200413119. Epub 2022 May 16. PMID: 35576468; PMCID: PMC9173764.

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72: Liao C, Castonguay CE, Heilbron K, Vuokila V, Medeiros M, Houle G, Akçimen F, Ross JP, Catoire H, Diez-Fairen M, Kang J, Mueller SH, Girard SL, Hopfner F, Lorenz D, Clark LN, Soto-Beasley AI, Klebe S, Hallett M, Wszolek ZK, Pendziwiat M, Lorenzo-Betancor O, Seppi K, Berg D, Vilariño-Güell C, Postuma RB, Bernard G, Dupré N, Jankovic J, Testa CM, Ross OA, Arzberger T, Chouinard S, Louis ED, Mandich P, Vitale C, Barone P, García-Martín E, Alonso-Navarro H, Agúndez JAG, Jiménez-Jiménez FJ, Pastor P, Rajput A, Deuschl G, Kuhlenbaümer G, Meijer IA, Dion PA, Rouleau GA; 23andMe Research Team. Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis. JAMA Neurol. 2022 Feb 1;79(2):185-193. doi: 10.1001/jamaneurol.2021.4781. Erratum in: JAMA Neurol. 2022 Jan 31;:null. PMID: 34982113; PMCID: PMC8728658.

73: Masnada S, Sarret C, Antonello CE, Fadilah A, Krude H, Mura E, Mordekar S, Nicita F, Olivotto S, Orcesi S, Porta F, Remerand G, Siri B, Wilpert NM, Amir- Yazdani P, Bertini E, Schuelke M, Bernard G, Boespflug-Tanguy O, Tonduti D. Movement disorders in MCT8 deficiency/Allan-Herndon-Dudley Syndrome. Mol Genet Metab. 2022 Jan;135(1):109-113. doi: 10.1016/j.ymgme.2021.12.003. Epub 2021 Dec 16. PMID: 34969638.

74: Luo JXX, Cui QL, Yaqubi M, Hall JA, Dudley R, Srour M, Addour N, Jamann H, Larochelle C, Blain M, Healy LM, Stratton JA, Sonnen JA, Kennedy TE, Antel JP. Human Oligodendrocyte Myelination Potential; Relation to Age and Differentiation. Ann Neurol. 2022 Feb;91(2):178-191. doi: 10.1002/ana.26288. Epub 2022 Jan 10. PMID: 34952986.

75: Mercuri E, Deconinck N, Mazzone ES, Nascimento A, Oskoui M, Saito K, Vuillerot C, Baranello G, Boespflug-Tanguy O, Goemans N, Kirschner J, Kostera- Pruszczyk A, Servais L, Gerber M, Gorni K, Khwaja O, Kletzl H, Scalco RS, Staunton H, Yeung WY, Martin C, Fontoura P, Day JW; SUNFISH Study Group. Safety and efficacy of once-daily risdiplam in type 2 and non-ambulant type 3 spinal muscular atrophy (SUNFISH part 2): a phase 3, double-blind, randomised, placebo- controlled trial. Lancet Neurol. 2022 Jan;21(1):42-52. doi: 10.1016/S1474-4422(21)00367-7. Erratum in: Lancet Neurol. 2022 Feb;21(2):e2. Erratum in: Lancet Neurol. 2022 Mar;21(3):e3. Erratum in: Lancet Neurol. 2022 May;21(5):e5. PMID: 34942136.

76: Mirza AI, Zhu F, Knox N, Forbes JD, Van Domselaar G, Bernstein CN, Graham M, Marrie RA, Hart J, Yeh EA, Arnold DL, Bar-Or A, O'Mahony J, Zhao Y, Hsiao W, Banwell B, Waubant E, Tremlett H. Metagenomic Analysis of the Pediatric-Onset Multiple Sclerosis Gut Microbiome. Neurology. 2022 Mar 8;98(10):e1050-e1063. doi: 10.1212/WNL.0000000000013245. Epub 2021 Dec 22. PMID: 34937787; PMCID: PMC8967388.

77: Howden K, Chapman S, Serletis D, Kazina C, Rafay MF, Faury D, Hazrati LN, Jabado N, Vanan MI. Management of Inoperable Supra-Sellar Low-Grade Glioma With BRAF Mutation in Young Children. Cureus. 2021 Nov 9;13(11):e19400. doi: 10.7759/cureus.19400. PMID: 34926002; PMCID: PMC8656291.

78: Mullins N, Kang J, Campos AI, Coleman JRI, Edwards AC, Galfalvy H, Levey DF, Lori A, Shabalin A, Starnawska A, Su MH, Watson HJ, Adams M, Awasthi S, Gandal M, Hafferty JD, Hishimoto A, Kim M, Okazaki S, Otsuka I, Ripke S, Ware EB, Bergen AW, Berrettini WH, Bohus M, Brandt H, Chang X, Chen WJ, Chen HC, Crawford S, Crow S, DiBlasi E, Duriez P, Fernández-Aranda F, Fichter MM, Gallinger S, Glatt SJ, Gorwood P, Guo Y, Hakonarson H, Halmi KA, Hwu HG, Jain S, Jamain S, Jiménez-Murcia S, Johnson C, Kaplan AS, Kaye WH, Keel PK, Kennedy JL, Klump KL, Li D, Liao SC, Lieb K, Lilenfeld L, Liu CM, Magistretti PJ, Marshall CR, Mitchell JE, Monson ET, Myers RM, Pinto D, Powers A, Ramoz N, Roepke S, Rozanov V, Scherer SW, Schmahl C, Sokolowski M, Strober M, Thornton LM, Treasure J, Tsuang MT, Witt SH, Woodside DB, Yilmaz Z, Zillich L, Adolfsson R, Agartz I, Air TM, Alda M, Alfredsson L, Andreassen OA, Anjorin A, Appadurai V, Soler Artigas M, Van der Auwera S, Azevedo MH, Bass N, Bau CHD, Baune BT, Bellivier F, Berger K, Biernacka JM, Bigdeli TB, Binder EB, Boehnke M, Boks MP, Bosch R, Braff DL, Bryant R, Budde M, Byrne EM, Cahn W, Casas M, Castelao E, Cervilla JA, Chaumette B, Cichon S, Corvin A, Craddock N, Craig D, Degenhardt F, Djurovic S, Edenberg HJ, Fanous AH, Foo JC, Forstner AJ, Frye M, Fullerton JM, Gatt JM, Gejman PV, Giegling I, Grabe HJ, Green MJ, Grevet EH, Grigoroiu-Serbanescu M, Gutierrez B, Guzman-Parra J, Hamilton SP, Hamshere ML, Hartmann A, Hauser J, Heilmann- Heimbach S, Hoffmann P, Ising M, Jones I, Jones LA, Jonsson L, Kahn RS, Kelsoe JR, Kendler KS, Kloiber S, Koenen KC, Kogevinas M, Konte B, Krebs MO, Landén M, Lawrence J, Leboyer M, Lee PH, Levinson DF, Liao C, Lissowska J, Lucae S, Mayoral F, McElroy SL, McGrath P, McGuffin P, McQuillin A, Medland SE, Mehta D, Melle I, Milaneschi Y, Mitchell PB, Molina E, Morken G, Mortensen PB, Müller- Myhsok B, Nievergelt C, Nimgaonkar V, Nöthen MM, O'Donovan MC, Ophoff RA, Owen MJ, Pato C, Pato MT, Penninx BWJH, Pimm J, Pistis G, Potash JB, Power RA, Preisig M, Quested D, Ramos-Quiroga JA, Reif A, Ribasés M, Richarte V, Rietschel M, Rivera M, Roberts A, Roberts G, Rouleau GA, Rovaris DL, Rujescu D, Sánchez- Mora C, Sanders AR, Schofield PR, Schulze TG, Scott LJ, Serretti A, Shi J, Shyn SI, Sirignano L, Sklar P, Smeland OB, Smoller JW, Sonuga-Barke EJS, Spalletta G, Strauss JS, Świątkowska B, Trzaskowski M, Turecki G, Vilar-Ribó L, Vincent JB, Völzke H, Walters JTR, Shannon Weickert C, Weickert TW, Weissman MM, Williams LM, Wray NR, Zai CC, Ashley-Koch AE, Beckham JC, Hauser ER, Hauser MA, Kimbrel NA, Lindquist JH, McMahon B, Oslin DW, Qin X; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium; Bipolar Disorder Working Group of the Psychiatric Genomics Consortium; Eating Disorders Working Group of the Psychiatric Genomics Consortium; German Borderline Genomics Consortium; MVP Suicide Exemplar Workgroup; VA Million Veteran Program, Agerbo E, Børglum AD, Breen G, Erlangsen A, Esko T, Gelernter J, Hougaard DM, Kessler RC, Kranzler HR, Li QS, Martin NG, McIntosh AM, Mors O, Nordentoft M, Olsen CM, Porteous D, Ursano RJ, Wasserman D, Werge T, Whiteman DC, Bulik CM, Coon H, Demontis D, Docherty AR, Kuo PH, Lewis CM, Mann JJ, Rentería ME, Smith DJ, Stahl EA, Stein MB, Streit F, Willour V, Ruderfer DM. Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors. Biol Psychiatry. 2022 Feb 1;91(3):313-327. doi: 10.1016/j.biopsych.2021.05.029. Epub 2021 Sep 9. PMID: 34861974; PMCID: PMC8851871.

79: Moreau JT, Simard-Tremblay E, Albrecht S, Rosenblatt B, Baillet S, Dudley RWR. Overnight Ictal Magnetoencephalography. Neurol Clin Pract. 2021 Oct;11(5):e732-e735. doi: 10.1212/CPJ.0000000000000937. PMID: 34840892; PMCID: PMC8610549.

80: Tran TPY, Pouliot P, Assi EB, Rainville P, Myers KA, Robert M, Bouthillier A, Keezer MR, Nguyen DK. Heart Rate Variability in Insulo-Opercular Epilepsy. Brain Sci. 2021 Nov 13;11(11):1505. doi: 10.3390/brainsci11111505. PMID: 34827504; PMCID: PMC8615554.

81: Estiar MA, Lail N, Dyment DA, Varghaei P, Hartley T, Gillespie MK, Yoon G, Boycott KM, Rouleau GA, Gan-Or Z. Heterozygous De Novo KPNA3 Mutations Cause Complex Hereditary Spastic Paraplegia. Ann Neurol. 2022 May;91(5):730-732. doi: 10.1002/ana.26275. Epub 2021 Dec 14. PMID: 34825409.

82: Suchowersky O, Ashtiani S, Au PB, McLeod S, Estiar MA, Gan-Or Z, Rouleau GA. Hereditary spastic paraplegia initially diagnosed as cerebral palsy. Clin Park Relat Disord. 2021 Nov 3;5:100114. doi: 10.1016/j.prdoa.2021.100114. PMID: 34816117; PMCID: PMC8592889.

83: Sahly AN, Shevell M, Sadleir LG, Myers KA. SUDEP risk and autonomic dysfunction in genetic epilepsies. Auton Neurosci. 2022 Jan;237:102907. doi: 10.1016/j.autneu.2021.102907. Epub 2021 Nov 10. PMID: 34773737.

84: Perrier S, Gauquelin L, Wambach JA, Bernard G. Distinguishing severe phenotypes associated with pathogenic variants in POLR3A. Am J Med Genet A. 2022 Feb;188(2):708-712. doi: 10.1002/ajmg.a.62553. Epub 2021 Nov 12. PMID: 34773388; PMCID: PMC8758552.

85: Geva M, Gershoni-Emek N, Naia L, Ly P, Mota S, Rego AC, Hayden MR, Levin LA. Neuroprotection of retinal ganglion cells by the sigma-1 receptor agonist pridopidine in models of experimental glaucoma. Sci Rep. 2021 Nov 9;11(1):21975. doi: 10.1038/s41598-021-01077-w. PMID: 34753986; PMCID: PMC8578336.

86: Vears DF, Minion JT, Roberts SJ, Cummings J, Machirori M, Blell M, Budin- Ljøsne I, Cowley L, Dyke SOM, Gaff C, Green R, Hall A, Johns AL, Knoppers BM, Mulrine S, Patch C, Winkler E, Murtagh MJ. Return of individual research results from genomic research: A systematic review of stakeholder perspectives. PLoS One. 2021 Nov 8;16(11):e0258646. doi: 10.1371/journal.pone.0258646. PMID: 34748551; PMCID: PMC8575249.

87: Klostranec JM, Vucevic D, Bhatia KD, Kortman HGJ, Krings T, Murphy KP, terBrugge KG, Mikulis DJ. Current Concepts in Intracranial Interstitial Fluid Transport and the Glymphatic System: Part II-Imaging Techniques and Clinical Applications. Radiology. 2021 Dec;301(3):516-532. doi: 10.1148/radiol.2021204088. Epub 2021 Oct 26. PMID: 34698564.

88: Lazow MA, Fuller C, DeWire M, Lane A, Bandopadhayay P, Bartels U, Bouffet E, Cheng S, Cohen KJ, Cooney TM, Coven SL, Dholaria H, Diez B, Dorris K, El-Ayadi M, El-Sheikh A, Fisher PG, Fonseca A, Garcia Lombardi M, Greiner RJ, Goldman S, Gottardo N, Gururangan S, Hansford JR, Hassall T, Hawkins C, Kilburn L, Koschmann C, Leary SE, Ma J, Minturn JE, Monje-Deisseroth M, Packer R, Samson Y, Sandler ES, Sevlever G, Tinkle CL, Tsui K, Wagner LM, Zaghloul M, Ziegler DS, Chaney B, Black K, Asher A, Drissi R, Fouladi M, Jones BV, Leach JL. Accuracy of central neuro-imaging review of DIPG compared with histopathology in the International DIPG Registry. Neuro Oncol. 2022 May 4;24(5):821-833. doi: 10.1093/neuonc/noab245. PMID: 34668975; PMCID: PMC9071293.

89: Klostranec JM, Vucevic D, Bhatia KD, Kortman HGJ, Krings T, Murphy KP, terBrugge KG, Mikulis DJ. Current Concepts in Intracranial Interstitial Fluid Transport and the Glymphatic System: Part I-Anatomy and Physiology. Radiology. 2021 Dec;301(3):502-514. doi: 10.1148/radiol.2021202043. Epub 2021 Oct 19. PMID: 34665028.

90: Bhatia KD, Lee H, Kortman H, Klostranec J, Guest W, Wälchli T, Radovanovic I, Krings T, Pereira VM. Endovascular Management of Intracranial Dural AVFs: Transvenous Approach. AJNR Am J Neuroradiol. 2022 Apr;43(4):510-516. doi: 10.3174/ajnr.A7300. Epub 2021 Oct 14. PMID: 34649915; PMCID: PMC8993200.

91: Munot P, McCrea N, Torelli S, Manzur A, Sewry C, Chambers D, Feng L, Ala P, Zaharieva I, Ragge N, Roper H, Marton T, Cox P, Milev MP, Liang WC, Maruyama S, Nishino I, Sacher M, Phadke R, Muntoni F. TRAPPC11-related muscular dystrophy with hypoglycosylation of alpha-dystroglycan in skeletal muscle and brain. Neuropathol Appl Neurobiol. 2022 Feb;48(2):e12771. doi: 10.1111/nan.12771. Epub 2021 Nov 11. PMID: 34648194.

92: Ashour M, Fortin O, Parent L, Sébire G, Saint-Martin C, Poulin C, Dudley R. Hirayama Disease in a Patient with a History of Late-Onset Symptomatic Vein of Galen Aneurysmal Malformation. Pediatr Neurosurg. 2021;56(6):555-562. doi: 10.1159/000519178. Epub 2021 Oct 11. PMID: 34634788.

93: Schur S, Moreau JT, Khoo HM, Koupparis A, Simard Tremblay E, Myers KA, Osterman B, Rosenblatt B, Farmer JP, Saint-Martin C, Turpin S, Hall J, Olivier A, Bernasconi A, Bernasconi N, Baillet S, Dubeau F, Gotman J, Dudley RWR. New interinstitutional, multimodal presurgical evaluation protocol associated with improved seizure freedom for poorly defined cases of focal epilepsy in children. J Neurosurg Pediatr. 2021 Oct 8;29(1):74-82. doi: 10.3171/2021.6.PEDS218. PMID: 34624842.

94: Wang S, Sun MZ, Abecassis IJ, Weil AG, Ibrahim GM, Fallah A, Ene C, Leary SES, Cole BL, Lockwood CM, Olson JM, Geyer JR, Ellenbogen RG, Ojemann JG, Wang AC. Predictors of mortality and tumor recurrence in desmoplastic infantile ganglioglioma and astrocytoma-and individual participant data meta-analysis (IPDMA). J Neurooncol. 2021 Nov;155(2):155-163. doi: 10.1007/s11060-021-03860-1. Epub 2021 Oct 6. PMID: 34613581; PMCID: PMC9448015.

95: Lemire G, Ito YA, Marshall AE, Chrestian N, Stanley V, Brady L, Tarnopolsky M, Curry CJ, Hartley T, Mears W, Derksen A, Rioux N, Laflamme N, Hutchison HT, Pais LS, Zaki MS, Sultan T, Dane AD; Care4Rare Canada Consortium, Gleeson JG, Vaz FM, Kernohan KD, Bernard G, Boycott KM. ABHD16A deficiency causes a complicated form of hereditary spastic paraplegia associated with intellectual disability and cerebral anomalies. Am J Hum Genet. 2021 Oct 7;108(10):2017-2023. doi: 10.1016/j.ajhg.2021.09.005. Epub 2021 Sep 28. PMID: 34587489; PMCID: PMC8546048.

96: Abdul Jafar NK, Tham EKH, Pang WW, Fok D, Chua MC, Teoh OH, Goh DYT, Shek LP, Yap F, Tan KH, Gluckman PD, Chong YS, Meaney MJ, Broekman BFP, Cai S. Association between breastfeeding and sleep patterns in infants and preschool children. Am J Clin Nutr. 2021 Dec 1;114(6):1986-1996. doi: 10.1093/ajcn/nqab297. PMID: 34582549.

97: Myers KA, Scheffer IE. Precision Medicine Approaches for Infantile-Onset Developmental and Epileptic Encephalopathies. Annu Rev Pharmacol Toxicol. 2022 Jan 6;62:641-662. doi: 10.1146/annurev-pharmtox-052120-084449. Epub 2021 Sep 27. PMID: 34579535.

98: Kalantar-Hormozi A, Moradi E, Hashemi SZ, Kalantar-Hormozi H, Abbaszadeh- Kasbi A. The Effect of Using In Vitro Fertilization (IVF) on Increasing the Prevalence of Craniosynostosis. J Craniofac Surg. 2022 Jan-Feb 01;33(1):26-28. doi: 10.1097/SCS.0000000000008188. PMID: 34545049.

99: Larivière S, Federico P, Chinvarun Y, Jackson G, Morgan V, Rampp S, Vaudano AE, Wang I, Cendes F, Boelman CG, Bernasconi A, Bernasconi N, Bernhardt BC, Schrader DV. ILAE Neuroimaging Task Force Highlight: harnessing optimized imaging protocols for drug-resistant childhood epilepsy. Epileptic Disord. 2021 Oct 1;23(5):675-681. doi: 10.1684/epd.2021.1312. PMID: 34526291.

100: Fallah A, Lewis E, Ibrahim GM, Kola O, Tseng CH, Harris WB, Chen JS, Lin KM, Cai LX, Liu QZ, Lin JL, Zhou WJ, Mathern GW, Smyth MD, O'Neill BR, Dudley RWR, Ragheb J, Bhatia S, Delev D, Ramantani G, Zentner J, Wang AC, Dorfer C, Feucht M, Czech T, Bollo RJ, Issabekov G, Zhu H, Connolly M, Steinbok P, Zhang JG, Zhang K, Hidalgo ET, Weiner HL, Wong-Kisiel L, Lapalme-Remis S, Tripathi M, Sarat Chandra P, Hader W, Wang FP, Yao Y, Champagne PO, Brunette-Clément T, Guo Q, Li SC, Budke M, Pérez-Jiménez MA, Raftopoulos C, Finet P, Michel P, Schaller K, Stienen MN, Baro V, Cantillano Malone C, Pociecha J, Chamorro N, Muro VL, von Lehe M, Vieker S, Oluigbo C, Gaillard WD, Al-Khateeb M, Al Otaibi F, Krayenbühl N, Bolton J, Pearl PL, Weil AG. Comparison of the real-world effectiveness of vertical versus lateral functional hemispherotomy techniques for pediatric drug- resistant epilepsy: A post hoc analysis of the HOPS study. Epilepsia. 2021 Nov;62(11):2707-2718. doi: 10.1111/epi.17021. Epub 2021 Sep 12. PMID: 34510448; PMCID: PMC9290517.

101: Johnson JO, Chia R, Miller DE, Li R, Kumaran R, Abramzon Y, Alahmady N, Renton AE, Topp SD, Gibbs JR, Cookson MR, Sabir MS, Dalgard CL, Troakes C, Jones AR, Shatunov A, Iacoangeli A, Al Khleifat A, Ticozzi N, Silani V, Gellera C, Blair IP, Dobson-Stone C, Kwok JB, Bonkowski ES, Palvadeau R, Tienari PJ, Morrison KE, Shaw PJ, Al-Chalabi A, Brown RH Jr, Calvo A, Mora G, Al-Saif H, Gotkine M, Leigh F, Chang IJ, Perlman SJ, Glass I, Scott AI, Shaw CE, Basak AN, Landers JE, Chiò A, Crawford TO, Smith BN, Traynor BJ; FALS Sequencing Consortium; American Genome Center; International ALS Genomics Consortium; and ITALSGEN Consortium, Smith BN, Ticozzi N, Fallini C, Gkazi AS, Topp SD, Scotter EL, Kenna KP, Keagle P, Tiloca C, Vance C, Troakes C, Colombrita C, King A, Pensato V, Castellotti B, Baas F, Ten Asbroek ALMA, McKenna-Yasek D, McLaughlin RL, Polak M, Asress S, Esteban-Pérez J, Stevic Z, D'Alfonso S, Mazzini L, Comi GP, Del Bo R, Ceroni M, Gagliardi S, Querin G, Bertolin C, van Rheenen W, Rademakers R, van Blitterswijk M, Lauria G, Duga S, Corti S, Cereda C, Corrado L, Sorarù G, Williams KL, Nicholson GA, Blair IP, Leblond-Manry C, Rouleau GA, Hardiman O, Morrison KE, Veldink JH, van den Berg LH, Al-Chalabi A, Pall H, Shaw PJ, Turner MR, Talbot K, Taroni F, García-Redondo A, Wu Z, Glass JD, Gellera C, Ratti A, Brown RH Jr, Silani V, Shaw CE, Landers JE, Dalgard CL, Adeleye A, Soltis AR, Alba C, Viollet C, Bacikova D, Hupalo DN, Sukumar G, Pollard HB, Wilkerson MD, Martinez EM, Abramzon Y, Ahmed S, Arepalli S, Baloh RH, Bowser R, Brady CB, Brice A, Broach J, Campbell RH, Camu W, Chia R, Cooper-Knock J, Ding J, Drepper C, Drory VE, Dunckley TL, Eicher JD, England BK, Faghri F, Feldman E, Floeter MK, Fratta P, Geiger JT, Gerhard G, Gibbs JR, Gibson SB, Glass JD, Hardy J, Harms MB, Heiman-Patterson TD, Hernandez DG, Jansson L, Kirby J, Kowall NW, Laaksovirta H, Landeck N, Landi F, Le Ber I, Lumbroso S, MacGowan DJL, Maragakis NJ, Mora G, Mouzat K, Murphy NA, Myllykangas L, Nalls MA, Orrell RW, Ostrow LW, Pamphlett R, Pickering-Brown S, Pioro EP, Pletnikova O, Pliner HA, Pulst SM, Ravits JM, Renton AE, Rivera A, Robberecht W, Rogaeva E, Rollinson S, Rothstein JD, Scholz SW, Sendtner M, Shaw PJ, Sidle KC, Simmons Z, Singleton AB, Smith N, Stone DJ, Tienari PJ, Troncoso JC, Valori M, Van Damme P, Van Deerlin VM, Van Den Bosch L, Zinman L, Landers JE, Chiò A, Traynor BJ, Angelocola SM, Ausiello FP, Barberis M, Bartolomei I, Battistini S, Bersano E, Bisogni G, Borghero G, Brunetti M, Cabona C, Calvo A, Canale F, Canosa A, Cantisani TA, Capasso M, Caponnetto C, Cardinali P, Carrera P, Casale F, Chiò A, Colletti T, Conforti FL, Conte A, Conti E, Corbo M, Cuccu S, Dalla Bella E, D'Errico E, DeMarco G, Dubbioso R, Ferrarese C, Ferraro PM, Filippi M, Fini N, Floris G, Fuda G, Gallone S, Gianferrari G, Giannini F, Grassano M, Greco L, Iazzolino B, Introna A, La Bella V, Lattante S, Lauria G, Liguori R, Logroscino G, Logullo FO, Lunetta C, Mandich P, Mandrioli J, Manera U, Manganelli F, Marangi G, Marinou K, Marrosu MG, Martinelli I, Messina S, Moglia C, Mora G, Mosca L, Murru MR, Origone P, Passaniti C, Petrelli C, Petrucci A, Pozzi S, Pugliatti M, Quattrini A, Ricci C, Riolo G, Riva N, Russo M, Sabatelli M, Salamone P, Salivetto M, Salvi F, Santarelli M, Sbaiz L, Sideri R, Simone I, Simonini C, Spataro R, Tanel R, Tedeschi G, Ticca A, Torriello A, Tranquilli S, Tremolizzo L, Trojsi F, Vasta R, Vacchiano V, Vita G, Volanti P, Zollino M, Zucchi E. Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis. JAMA Neurol. 2021 Oct 1;78(10):1236-1248. doi: 10.1001/jamaneurol.2021.2598. PMID: 34459874; PMCID: PMC8406220.

102: Helman G, Mendes MI, Nicita F, Darbelli L, Sherbini O, Moore T, Derksen A, Amy Pizzino, Carrozzo R, Torraco A, Catteruccia M, Aiello C, Goffrini P, Figuccia S, Smith DEC, Hadzsiev K, Hahn A, Biskup S, Brösse I, Kotzaeridou U, Gauck D, Grebe TA, Elmslie F, Stals K, Gupta R, Bertini E, Thiffault I, Taft RJ, Schiffmann R, Brandl U, Haack TB, Salomons GS, Simons C, Bernard G, van der Knaap MS, Vanderver A, Husain RA. Expanded phenotype of AARS1-related white matter disease. Genet Med. 2021 Dec;23(12):2352-2359. doi: 10.1038/s41436-021-01286-8. Epub 2021 Aug 27. PMID: 34446925.

103: Levitis E, van Praag CDG, Gau R, Heunis S, DuPre E, Kiar G, Bottenhorn KL, Glatard T, Nikolaidis A, Whitaker KJ, Mancini M, Niso G, Afyouni S, Alonso-Ortiz E, Appelhoff S, Arnatkeviciute A, Atay SM, Auer T, Baracchini G, Bayer JMM, Beauvais MJS, Bijsterbosch JD, Bilgin IP, Bollmann S, Bollmann S, Botvinik-Nezer R, Bright MG, Calhoun VD, Chen X, Chopra S, Chuan-Peng H, Close TG, Cookson SL, Craddock RC, De La Vega A, De Leener B, Demeter DV, Di Maio P, Dickie EW, Eickhoff SB, Esteban O, Finc K, Frigo M, Ganesan S, Ganz M, Garner KG, Garza- Villarreal EA, Gonzalez-Escamilla G, Goswami R, Griffiths JD, Grootswagers T, Guay S, Guest O, Handwerker DA, Herholz P, Heuer K, Huijser DC, Iacovella V, Joseph MJE, Karakuzu A, Keator DB, Kobeleva X, Kumar M, Laird AR, Larson-Prior LJ, Lautarescu A, Lazari A, Legarreta JH, Li XY, Lv J, Mansour L S, Meunier D, Moraczewski D, Nandi T, Nastase SA, Nau M, Noble S, Norgaard M, Obungoloch J, Oostenveld R, Orchard ER, Pinho AL, Poldrack RA, Qiu A, Raamana PR, Rokem A, Rutherford S, Sharan M, Shaw TB, Syeda WT, Testerman MM, Toro R, Valk SL, Van Den Bossche S, Varoquaux G, Váša F, Veldsman M, Vohryzek J, Wagner AS, Walsh RJ, White T, Wong FT, Xie X, Yan CG, Yang YF, Yee Y, Zanitti GE, Van Gulick AE, Duff E, Maumet C. Centering inclusivity in the design of online conferences-An OHBM- Open Science perspective. Gigascience. 2021 Aug 20;10(8):giab051. doi: 10.1093/gigascience/giab051. PMID: 34414422; PMCID: PMC8377301.

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105: Koupparis A, von Ellenrieder N, Khoo HM, Zazubovits N, Nguyen DK, Hall JA, Dudley RWR, Dubeau F, Gotman J. Association of EEG-fMRI Responses and Outcome After Epilepsy Surgery. Neurology. 2021 Aug 16;97(15):e1523–36. doi: 10.1212/WNL.0000000000012660. Epub ahead of print. PMID: 34400584; PMCID: PMC8575131.

106: Zhang M, Wong SW, Wright JN, Toescu S, Mohammadzadeh M, Han M, Lummus S, Wagner MW, Yecies D, Lai H, Eghbal A, Radmanesh A, Nemelka J, Harward S, Malinzak M, Laughlin S, Perreault S, Braun KRM, Vossough A, Poussaint T, Goetti R, Ertl-Wagner B, Ho CY, Oztekin O, Ramaswamy V, Mankad K, Vitanza NA, Cheshier SH, Said M, Aquilina K, Thompson E, Jaju A, Grant GA, Lober RM, Yeom KW. Machine Assist for Pediatric Posterior Fossa Tumor Diagnosis: A Multinational Study. Neurosurgery. 2021 Oct 13;89(5):892-900. doi: 10.1093/neuros/nyab311. PMID: 34392363; PMCID: PMC8764569.

107: Galosi S, Edani BH, Martinelli S, Hansikova H, Eklund EA, Caputi C, Masuelli L, Corsten-Janssen N, Srour M, Oegema R, Bosch DGM, Ellis CA, Amlie- Wolf L, Accogli A, Atallah I, Averdunk L, Barañano KW, Bei R, Bagnasco I, Brusco A, Demarest S, Alaix AS, Di Bonaventura C, Distelmaier F, Elmslie F, Gan-Or Z, Good JM, Gripp K, Kamsteeg EJ, Macnamara E, Marcelis C, Mercier N, Peeden J, Pizzi S, Pannone L, Shinawi M, Toro C, Verbeek NE, Venkateswaran S, Wheeler PG, Zdrazilova L, Zhang R, Zorzi G, Guerrini R, Sessa WC, Lefeber DJ, Tartaglia M, Hamdan FF, Grabińska KA, Leuzzi V. De novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonus. Brain. 2022 Mar 29;145(1):208-223. doi: 10.1093/brain/awab299. PMID: 34382076; PMCID: PMC8967098.

108: Vitagliano M, Dunbar M, Dyck Holzinger S, Letourneau N, Dewey D, Oskoui M, Shevell M, Kirton A. Perinatal arterial ischemic stroke and periventricular venous infarction in infants with unilateral cerebral palsy. Dev Med Child Neurol. 2022 Jan;64(1):56-62. doi: 10.1111/dmcn.15000. Epub 2021 Aug 10. PMID: 34374437.

109: Sievers P, Henneken SC, Blume C, Sill M, Schrimpf D, Stichel D, Okonechnikov K, Reuss DE, Benzel J, Maaß KK, Kool M, Sturm D, Zheng T, Ghasemi DR, Kohlhof-Meinecke P, Cruz O, Suñol M, Lavarino C, Ruf V, Boldt HB, Pagès M, Pouget C, Schweizer L, Kranendonk MEG, Akhtar N, Bunkowski S, Stadelmann C, Schüller U, Mueller WC, Dohmen H, Acker T, Harter PN, Mawrin C, Beschorner R, Brandner S, Snuderl M, Abdullaev Z, Aldape K, Gilbert MR, Armstrong TS, Ellison DW, Capper D, Ichimura K, Reifenberger G, Grundy RG, Jabado N, Krskova L, Zapotocky M, Vicha A, Varlet P, Wesseling P, Rutkowski S, Korshunov A, Wick W, Pfister SM, Jones DTW, von Deimling A, Pajtler KW, Sahm F. Recurrent fusions in PLAGL1 define a distinct subset of pediatric-type supratentorial neuroepithelial tumors. Acta Neuropathol. 2021 Nov;142(5):827-839. doi: 10.1007/s00401-021-02356-6. Epub 2021 Aug 5. PMID: 34355256; PMCID: PMC8500895.

110: Myers KA. Response: Sotos Syndrome and the added value of genetic workup in epilepsy surgery. Epilepsia Open. 2021 Dec;6(4):795-796. doi: 10.1002/epi4.12528. Epub 2021 Aug 5. PMID: 34351709; PMCID: PMC8633461.

111: Gleichgerrcht E, Munsell BC, Alhusaini S, Alvim MKM, Bargalló N, Bender B, Bernasconi A, Bernasconi N, Bernhardt B, Blackmon K, Caligiuri ME, Cendes F, Concha L, Desmond PM, Devinsky O, Doherty CP, Domin M, Duncan JS, Focke NK, Gambardella A, Gong B, Guerrini R, Hatton SN, Kälviäinen R, Keller SS, Kochunov P, Kotikalapudi R, Kreilkamp BAK, Labate A, Langner S, Larivière S, Lenge M, Lui E, Martin P, Mascalchi M, Meletti S, O'Brien TJ, Pardoe HR, Pariente JC, Xian Rao J, Richardson MP, Rodríguez-Cruces R, Rüber T, Sinclair B, Soltanian-Zadeh H, Stein DJ, Striano P, Taylor PN, Thomas RH, Elisabetta Vaudano A, Vivash L, von Podewills F, Vos SB, Weber B, Yao Y, Lin Yasuda C, Zhang J, Thompson PM, Sisodiya SM, McDonald CR, Bonilha L; ENIGMA-Epilepsy Working Group. Artificial intelligence for classification of temporal lobe epilepsy with ROI-level MRI data: A worldwide ENIGMA-Epilepsy study. Neuroimage Clin. 2021;31:102765. doi: 10.1016/j.nicl.2021.102765. Epub 2021 Jul 24. PMID: 34339947; PMCID: PMC8346685.

112: Nowicki M, Bourgeois-Tardif S, Diaz PL, Hebert FO, Sanon NT, Champagne PO, Major P, Sell E, Bitton J, Lewis E, Weil AG. Potential Benefit of Add-on Δ9-Tetrahydrocannabinol in Pediatric Drug-Resistant Epilepsy: A Case Series. Can J Neurol Sci. 2022 Jul;49(4):595-597. doi: 10.1017/cjn.2021.151. Epub 2021 Jun 29. PMID: 34183079.

113: Minato E, Myers KA. Age-related evolution of EEG in Dravet syndrome: Meta- analysis of 155 patients. Seizure. 2021 Oct;91:108-111. doi: 10.1016/j.seizure.2021.06.007. Epub 2021 Jun 11. PMID: 34147886.

114: Erker C, Lane A, Chaney B, Leary S, Minturn JE, Bartels U, Packer RJ, Dorris K, Gottardo NG, Warren KE, Broniscer A, Kieran MW, Zhu X, White P, Dexheimer PJ, Black K, Asher A, DeWire M, Hansford JR, Gururangan S, Nazarian J, Ziegler DS, Sandler E, Bartlett A, Goldman S, Shih CS, Hassall T, Dholaria H, Bandopadhayay P, Samson Y, Monje M, Fisher PG, Dodgshun A, Parkin S, Chintagumpala M, Tsui K, Gass D, Larouche V, Broxson E, Garcia Lombardi M, Wang SS, Ma J, Hawkins C, Hamideh D, Wagner L, Koschmann C, Fuller C, Drissi R, Jones BV, Leach J, Fouladi M. Characteristics of patients ≥10 years of age with diffuse intrinsic pontine glioma: a report from the International DIPG/DMG Registry. Neuro Oncol. 2022 Jan 5;24(1):141-152. doi: 10.1093/neuonc/noab140. PMID: 34114629; PMCID: PMC8730773.

115: Tremblay-Laganière C, Maroofian R, Nguyen TTM, Karimiani EG, Kirmani S, Akbar F, Ibrahim S, Afroze B, Doosti M, Ashrafzadeh F, Babaei M, Efthymiou S, Christoforou M, Sultan T, Ladda RL, McLaughlin HM, Truty R, Mahida S, Cohen JS, Baranano K, Ismail FY, Patel MS, Lehman A, Edmondson AC, Nagy A, Walker MA, Mercimek-Andrews S, Maki Y, Sachdev R, Macintosh R, Palmer EE, Mancini GMS, Barakat TS, Steinfeld R, Rüsch CT, Stettner GM, Wagner M, Wortmann SB, Kini U, Brady AF, Stals KL, Ismayilova N, Ellard S, Bernardo D, Nugent K, McLean SD, Antonarakis SE, Houlden H, Kinoshita T, Campeau PM, Murakami Y. PIGG variant pathogenicity assessment reveals characteristic features within 19 families. Genet Med. 2021 Oct;23(10):1873-1881. doi: 10.1038/s41436-021-01215-9. Epub 2021 Jun 10. PMID: 34113002.

116: Oskoui M, Gonorazky H, McMillan HJ, Dowling JJ, Amin R, Gagnon C, Selby K. Guidance on Gene Replacement Therapy in Spinal Muscular Atrophy: A Canadian Perspective. Can J Neurol Sci. 2022 May;49(3):398-401. doi: 10.1017/cjn.2021.125. Epub 2021 Jun 4. PMID: 34082851.

117: Bouhadoun S, Poulin C, Berrahmoune S, Myers KA. A retrospective analysis of memantine use in a pediatric neurology clinic. Brain Dev. 2021 Nov;43(10):997-1003. doi: 10.1016/j.braindev.2021.05.012. Epub 2021 May 29. PMID: 34074563.

118: Donovan LK, Delaidelli A, Joseph SK, Bielamowicz K, Fousek K, Holgado BL, Manno A, Srikanthan D, Gad AZ, Van Ommeren R, Przelicki D, Richman C, Ramaswamy V, Daniels C, Pallota JG, Douglas T, Joynt ACM, Haapasalo J, Nor C, Vladoiu MC, Kuzan-Fischer CM, Garzia L, Mack SC, Varadharajan S, Baker ML, Hendrikse L, Ly M, Kharas K, Balin P, Wu X, Qin L, Huang N, Stucklin AG, Morrissy AS, Cavalli FMG, Luu B, Suarez R, De Antonellis P, Michealraj A, Rastan A, Hegde M, Komosa M, Sirbu O, Kumar SA, Abdullaev Z, Faria CC, Yip S, Hukin J, Tabori U, Hawkins C, Aldape K, Daugaard M, Maris JM, Sorensen PH, Ahmed N, Taylor MD. Author Correction: Locoregional delivery of CAR T cells to the cerebrospinal fluid for treatment of metastatic medulloblastoma and ependymoma. Nat Med. 2021 Jun;27(6):1117-1120. doi: 10.1038/s41591-021-01362-1. Erratum for: Nat Med. 2020 May;26(5):720-731. PMID: 34045740.

119: Spinella PC, El Kassar N, Cap AP, Kindzelski AL, Almond CS, Barkun A, Gernsheimer TB, Goldstein JN, Holcomb JB, Iorio A, Jensen DM, Key NS, Levy JH, Mayer SA, Moore EE, Stanworth SJ, Lewis RJ, Steiner ME; Hemostasis Trials Outcomes Working Group. Recommended primary outcomes for clinical trials evaluating hemostatic blood products and agents in patients with bleeding: Proceedings of a National Heart Lung and Blood Institute and US Department of Defense Consensus Conference. J Trauma Acute Care Surg. 2021 Aug 1;91(2S Suppl 2):S19-S25. doi: 10.1097/TA.0000000000003300. PMID: 34039915; PMCID: PMC9032809.

120: Fortin O, Vincelette C, Khan AQ, Berrahmoune S, Dassi C, Karimi M, Scheffer IE, Lu J, Davis K, Myers KA. Seizures in Sotos syndrome: Phenotyping in 49 patients. Epilepsia Open. 2021 Jun;6(2):425-430. doi: 10.1002/epi4.12484. Epub 2021 Apr 9. PMID: 34033256; PMCID: PMC8166795.

121: Garbin M, Bertolizio G, Portela DA. Thoracic paravertebral block for an opioid-free thoracotomy in a dog. Vet Anaesth Analg. 2021 Jul;48(4):622-623. doi: 10.1016/j.vaa.2021.03.004. Epub 2021 Mar 20. PMID: 34006494.

122: Pathak R, Zin F, Thomas C, Bens S, Gayden T, Karamchandani J, Dudley RW, Nemes K, Johann PD, Oyen F, Kordes U, Jabado N, Siebert R, Paulus W, Kool M, Frühwald MC, Albrecht S, Kalpana GV, Hasselblatt M. Inhibition of nuclear export restores nuclear localization and residual tumor suppressor function of truncated SMARCB1/INI1 protein in a molecular subset of atypical teratoid/rhabdoid tumors. Acta Neuropathol. 2021 Aug;142(2):361-374. doi: 10.1007/s00401-021-02328-w. Epub 2021 May 18. PMID: 34003336; PMCID: PMC8270878.

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124: Weil AG, Fallah A, Wang S, Ibrahim GM, Elkaim LM, Jayakar P, Miller I, Bhatia S, Niazi TN, Ragheb J. Functional hemispherectomy: can preoperative imaging predict outcome? J Neurosurg Pediatr. 2020 Jun 1;25(6). doi: 10.3171/2019.12.PEDS19370. Epub 2020 Feb 21. PMID: 33988937.

125: Durno C, Ercan AB, Bianchi V, Edwards M, Aronson M, Galati M, Atenafu EG, Abebe-Campino G, Al-Battashi A, Alharbi M, Azad VF, Baris HN, Basel D, Bedgood R, Bendel A, Ben-Shachar S, Blumenthal DT, Blundell M, Bornhorst M, Bronsema A, Cairney E, Rhode S, Caspi S, Chamdin A, Chiaravalli S, Constantini S, Crooks B, Das A, Dvir R, Farah R, Foulkes WD, Frenkel Z, Gallinger B, Gardner S, Gass D, Ghalibafian M, Gilpin C, Goldberg Y, Goudie C, Hamid SA, Hampel H, Hansford JR, Harlos C, Hijiya N, Hsu S, Kamihara J, Kebudi R, Knipstein J, Koschmann C, Kratz C, Larouche V, Lassaletta A, Lindhorst S, Ling SC, Link MP, Loret De Mola R, Luiten R, Lurye M, Maciaszek JL, MagimairajanIssai V, Maher OM, Massimino M, McGee RB, Mushtaq N, Mason G, Newmark M, Nicholas G, Nichols KE, Nicolaides T, Opocher E, Osborn M, Oshrine B, Pearlman R, Pettee D, Rapp J, Rashid M, Reddy A, Reichman L, Remke M, Robbins G, Roy S, Sabel M, Samuel D, Scheers I, Schneider KW, Sen S, Stearns D, Sumerauer D, Swallow C, Taylor L, Thomas G, Toledano H, Tomboc P, Van Damme A, Winer I, Yalon M, Yen LY, Zapotocky M, Zelcer S, Ziegler DS, Zimmermann S, Hawkins C, Malkin D, Bouffet E, Villani A, Tabori U. Survival Benefit for Individuals With Constitutional Mismatch Repair Deficiency Undergoing Surveillance. J Clin Oncol. 2021 Sep 1;39(25):2779-2790. doi: 10.1200/JCO.20.02636. Epub 2021 May 4. PMID: 33945292; PMCID: PMC8407605.

126: Smith JS, Kelly MP, Yanik EL, Baldus CR, Buell TJ, Lurie JD, Edwards C, Glassman SD, Lenke LG, Boachie-Adjei O, Buchowski JM, Carreon LY, Crawford CH, Errico TJ, Lewis SJ, Koski T, Parent S, Lafage V, Kim HJ, Ames CP, Bess S, Schwab FJ, Shaffrey CI, Bridwell KH. Operative versus nonoperative treatment for adult symptomatic lumbar scoliosis at 5-year follow-up: durability of outcomes and impact of treatment-related serious adverse events. J Neurosurg Spine. 2021 Apr 30:1-13. doi: 10.3171/2020.9.SPINE201472. Epub ahead of print. PMID: 33930859.

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167: Mireault D, Cawthorn TR, Todd AR, Spencer AO. Suprazygomatic maxillary nerve block: an ultrasound and cadaveric study to identify correct sonoanatomical landmarks. J Anesth. 2021 Feb;35(1):150-153. doi: 10.1007/s00540-020-02877-6. Epub 2020 Nov 23. PMID: 33230676.

168: Bolduc ME, Dionne E, Gagnon I, Rennick JE, Majnemer A, Brossard-Racine M. Motor Impairment in Children With Congenital Heart Defects: A Systematic Review. Pediatrics. 2020 Dec;146(6):e20200083. doi: 10.1542/peds.2020-0083. PMID: 33208496.

169: Larivière S, Rodríguez-Cruces R, Royer J, Caligiuri ME, Gambardella A, Concha L, Keller SS, Cendes F, Yasuda C, Bonilha L, Gleichgerrcht E, Focke NK, Domin M, von Podewills F, Langner S, Rummel C, Wiest R, Martin P, Kotikalapudi R, O'Brien TJ, Sinclair B, Vivash L, Desmond PM, Alhusaini S, Doherty CP, Cavalleri GL, Delanty N, Kälviäinen R, Jackson GD, Kowalczyk M, Mascalchi M, Semmelroch M, Thomas RH, Soltanian-Zadeh H, Davoodi-Bojd E, Zhang J, Lenge M, Guerrini R, Bartolini E, Hamandi K, Foley S, Weber B, Depondt C, Absil J, Carr SJA, Abela E, Richardson MP, Devinsky O, Severino M, Striano P, Tortora D, Hatton SN, Vos SB, Duncan JS, Whelan CD, Thompson PM, Sisodiya SM, Bernasconi A, Labate A, McDonald CR, Bernasconi N, Bernhardt BC. Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA study. Sci Adv. 2020 Nov 18;6(47):eabc6457. doi: 10.1126/sciadv.abc6457. PMID: 33208365; PMCID: PMC7673818.

170: Teel E, Brossard-Racine M, Corbin-Berrigan LA, Gagnon I. Perceptual Cognitive Training Does Not Improve Clinical Outcomes at 4 and 12 Weeks Following Concussion in Children and Adolescents: A Randomized Controlled Trial. J Head Trauma Rehabil. 2021 Mar-Apr 01;36(2):E97-E107. doi: 10.1097/HTR.0000000000000633. PMID: 33201041.

171: Bakker MK, van der Spek RAA, van Rheenen W, Morel S, Bourcier R, Hostettler IC, Alg VS, van Eijk KR, Koido M, Akiyama M, Terao C, Matsuda K, Walters RG, Lin K, Li L, Millwood IY, Chen Z, Rouleau GA, Zhou S, Rannikmäe K, Sudlow CLM, Houlden H, van den Berg LH, Dina C, Naggara O, Gentric JC, Shotar E, Eugène F, Desal H, Winsvold BS, Børte S, Johnsen MB, Brumpton BM, Sandvei MS, Willer CJ, Hveem K, Zwart JA, Verschuren WMM, Friedrich CM, Hirsch S, Schilling S, Dauvillier J, Martin O; HUNT All-In Stroke; China Kadoorie Biobank Collaborative Group; BioBank Japan Project Consortium; ICAN Study Group; CADISP Group; Genetics and Observational Subarachnoid Haemorrhage (GOSH) Study investigators; International Stroke Genetics Consortium (ISGC), Jones GT, Bown MJ, Ko NU, Kim H, Coleman JRI, Breen G, Zaroff JG, Klijn CJM, Malik R, Dichgans M, Sargurupremraj M, Tatlisumak T, Amouyel P, Debette S, Rinkel GJE, Worrall BB, Pera J, Slowik A, Gaál-Paavola EI, Niemelä M, Jääskeläinen JE, von Und Zu Fraunberg M, Lindgren A, Broderick JP, Werring DJ, Woo D, Redon R, Bijlenga P, Kamatani Y, Veldink JH, Ruigrok YM. Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors. Nat Genet. 2020 Dec;52(12):1303-1313. doi: 10.1038/s41588-020-00725-7. Epub 2020 Nov 16. Erratum in: Nat Genet. 2020 Dec 22;: PMID: 33199917; PMCID: PMC7116530.

172: van Beinum A, Healey A, Chandler J, Dhanani S, Hartwick M, Lewis A, Marshall C, Marshall J, Shemie S, Singh JM. Requests for somatic support after neurologic death determination: Canadian physician experiences. Can J Anaesth. 2021 Mar;68(3):293-314. doi: 10.1007/s12630-020-01852-9. Epub 2020 Nov 10. Erratum in: Can J Anaesth. 2020 Nov 24;: PMID: 33174163; PMCID: PMC7654566.

173: Gauquelin L, Hartley T, Tarnopolsky M, Dyment DA, Brais B, Geraghty MT, Tétreault M, Ahmed S, Rojas S, Choquet K, Majewski J, Bernier F, Innes AM, Rouleau G, Suchowersky O, Boycott KM, Yoon G. Channelopathies Are a Frequent Cause of Genetic Ataxias Associated with Cerebellar Atrophy. Mov Disord Clin Pract. 2020 Sep 29;7(8):940-949. doi: 10.1002/mdc3.13086. PMID: 33163565; PMCID: PMC7604675.

174: Tremblay-Laganière C, Kaiyrzhanov R, Maroofian R, Nguyen TTM, Salayev K, Chilton IT, Chung WK, Madden JA, Phornphutkul C, Agrawal PB, Houlden H, Campeau PM. PIGH deficiency can be associated with severe neurodevelopmental and skeletal manifestations. Clin Genet. 2021 Feb;99(2):313-317. doi: 10.1111/cge.13877. Epub 2020 Nov 27. PMID: 33156547; PMCID: PMC7839508.

175: Weil AG, Mathews N, Farmer JP, St Martin C, Albrecht S, Jabado N, Dudley RWR. Successful treatment of non-midline primary malignant germ cell tumors with yolk sac components in neonates: report of 2 cases. J Neurosurg Pediatr. 2020 Oct 30;27(1):47-51. doi: 10.3171/2020.6.PEDS19719. PMID: 33126205.

176: Balakrishnan I, Danis E, Pierce A, Madhavan K, Wang D, Dahl N, Sanford B, Birks DK, Davidson N, Metselaar DS, Meel MH, Lemma R, Donson A, Vijmasi T, Katagi H, Sola I, Fosmire S, Alimova I, Steiner J, Gilani A, Hulleman E, Serkova NJ, Hashizume R, Hawkins C, Carcaboso AM, Gupta N, Monje M, Jabado N, Jones K, Foreman N, Green A, Vibhakar R, Venkataraman S. Senescence Induced by BMI1 Inhibition Is a Therapeutic Vulnerability in H3K27M-Mutant DIPG. Cell Rep. 2020 Oct 20;33(3):108286. doi: 10.1016/j.celrep.2020.108286. PMID: 33086074; PMCID: PMC7574900.

177: Appendino JP, Baker S, Chapman KM, Dykstra T, Hussein T, Jones ML, Mezei MM, Mirsattari SM, Ng M, Nikkel J, Obradovic V, Phan C, Robinson L, Scott A, Téllez-Zenteno J, Van Niekerk M, Venance S, Moore F. Response from Authors to the Letter to the Editor. Can J Neurol Sci. 2021 Jan;48(1):135-137. doi: 10.1017/cjn.2020.225. Epub 2020 Oct 15. PMID: 33054869; PMCID: PMC7853747.

178: Aravamuthan BR, Shevell M, Kim YM, Wilson JL, O'Malley JA, Pearson TS, Kruer MC, Fahey M, Waugh JL, Russman B, Shapiro B, Tilton A. Role of child neurologists and neurodevelopmentalists in the diagnosis of cerebral palsy: A survey study. Neurology. 2020 Nov 24;95(21):962-972. doi: 10.1212/WNL.0000000000011036. Epub 2020 Oct 12. PMID: 33046609; PMCID: PMC7734737.

179: van Lee L, Chia A, Phua D, Colega M, Padmapriya N, Bernard JY, Cai S, Tham EKH, Teoh OH, Goh D, Gooley JJ, Gluckman PD, Yap F, Shek LPC, Godfrey KM, Tan KH, Chong YS, Müller-Riemenschneider F, Broekman B, Meaney M, Chen H, Chong MFF. Multiple modifiable lifestyle factors and the risk of perinatal depression during pregnancy: Findings from the GUSTO cohort. Compr Psychiatry. 2020 Nov;103:152210. doi: 10.1016/j.comppsych.2020.152210. Epub 2020 Sep 30. PMID: 33045668.

180: Prince EW, Whelan R, Mirsky DM, Stence N, Staulcup S, Klimo P, Anderson RCE, Niazi TN, Grant G, Souweidane M, Johnston JM, Jackson EM, Limbrick DD Jr, Smith A, Drapeau A, Chern JJ, Kilburn L, Ginn K, Naftel R, Dudley R, Tyler- Kabara E, Jallo G, Handler MH, Jones K, Donson AM, Foreman NK, Hankinson TC. Robust deep learning classification of adamantinomatous craniopharyngioma from limited preoperative radiographic images. Sci Rep. 2020 Oct 9;10(1):16885. doi: 10.1038/s41598-020-73278-8. PMID: 33037266; PMCID: PMC7547020.

181: Myers KA. Response to Canadian Neurophysiology Laboratory COVID-19 Practice Guidelines. Can J Neurol Sci. 2021 Jan;48(1):133-134. doi: 10.1017/cjn.2020.220. Epub 2020 Oct 6. PMID: 33019956; PMCID: PMC7853735.

182: Pelletier F, Perrier S, Cayami FK, Mirchi A, Saikali S, Tran LT, Ulrick N, Guerrero K, Rampakakis E, van Spaendonk RML, Naidu S, Pohl D, Gibson WT, Demos M, Goizet C, Tejera-Martin I, Potic A, Fogel BL, Brais B, Sylvain M, Sébire G, Lourenço CM, Bonkowsky JL, Catsman-Berrevoets C, Pinto PS, Tirupathi S, Strømme P, de Grauw T, Gieruszczak-Bialek D, Krägeloh-Mann I, Mierzewska H, Philippi H, Rankin J, Atik T, Banwell B, Benko WS, Blaschek A, Bley A, Boltshauser E, Bratkovic D, Brozova K, Cimas I, Clough C, Corenblum B, Dinopoulos A, Dolan G, Faletra F, Fernandez R, Fletcher J, Garcia Garcia ME, Gasparini P, Gburek- Augustat J, Gonzalez Moron D, Hamati A, Harting I, Hertzberg C, Hill A, Hobson GM, Innes AM, Kauffman M, Kirwin SM, Kluger G, Kolditz P, Kotzaeridou U, La Piana R, Liston E, McClintock W, McEntagart M, McKenzie F, Melançon S, Misbahuddin A, Suri M, Monton FI, Moutton S, Murphy RPJ, Nickel M, Onay H, Orcesi S, Özkınay F, Patzer S, Pedro H, Pekic S, Pineda Marfa M, Pizzino A, Plecko B, Poll-The BT, Popovic V, Rating D, Rioux MF, Rodriguez Espinosa N, Ronan A, Ostergaard JR, Rossignol E, Sanchez-Carpintero R, Schossig A, Senbil N, Sønderberg Roos LK, Stevens CA, Synofzik M, Sztriha L, Tibussek D, Timmann D, Tonduti D, van de Warrenburg BP, Vázquez-López M, Venkateswaran S, Wasling P, Wassmer E, Webster RI, Wiegand G, Yoon G, Rotteveel J, Schiffmann R, van der Knaap MS, Vanderver A, Martos-Moreno GÁ, Polychronakos C, Wolf NI, Bernard G. Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C. J Clin Endocrinol Metab. 2021 Jan 23;106(2):e660-e674. doi: 10.1210/clinem/dgaa700. PMID: 33005949; PMCID: PMC7823228.

183: Cristini J, Weiss M, De Las Heras B, Medina-Rincón A, Dagher A, Postuma RB, Huber R, Doyon J, Rosa-Neto P, Carrier J, Amara AW, Roig M. The effects of exercise on sleep quality in persons with Parkinson's disease: A systematic review with meta-analysis. Sleep Med Rev. 2021 Feb;55:101384. doi: 10.1016/j.smrv.2020.101384. Epub 2020 Sep 8. PMID: 32987321.

184: Al-Roubaie Z, Guadagno E, Ramanakumar AV, Khan AQ, Myers KA. Clinical utility of therapeutic drug monitoring of antiepileptic drugs: Systematic review. Neurol Clin Pract. 2020 Aug;10(4):344-355. doi: 10.1212/CPJ.0000000000000722. PMID: 32983615; PMCID: PMC7508342.

185: Garbin M, Portela DA, Bertolizio G, Gallastegui A, Otero PE. A novel ultrasound-guided lateral quadratus lumborum block in dogs: a comparative cadaveric study of two approaches. Vet Anaesth Analg. 2020 Nov;47(6):810-818. doi: 10.1016/j.vaa.2020.08.003. Epub 2020 Aug 13. PMID: 32981838.

186: Yan H, Siegel L, Breitbart S, Gorodetsky C, Gonorazky HD, Yau I, Go C, Donner E, Kalia SK, Fasano A, Weil AG, Fallah A, Ibrahim GM. The Child & Youth CompreHensIve Longitudinal Database for Deep Brain Stimulation (CHILD-DBS). Childs Nerv Syst. 2021 Feb;37(2):607-615. doi: 10.1007/s00381-020-04880-4. Epub 2020 Sep 15. PMID: 32935233.

187: Beauregard-Lacroix E, Pacheco-Cuellar G, Ajeawung NF, Tardif J, Dieterich K, Dabir T, Vind-Kezunovic D, White SM, Zadori D, Castiglioni C, Tranebjærg L, Tørring PM, Blair E, Wisniewska M, Camurri MV, van Bever Y, Molidperee S, Taylor J, Dionne-Laporte A, Sisodiya SM, Hennekam RCM, Campeau PM. Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant. Genet Med. 2021 Jan;23(1):237. doi: 10.1038/s41436-020-00969-y. Erratum for: Genet Med. 2021 Jan;23(1):149-154. PMID: 32934366.

188: Douard E, Zeribi A, Schramm C, Tamer P, Loum MA, Nowak S, Saci Z, Lord MP, Rodríguez-Herreros B, Jean-Louis M, Moreau C, Loth E, Schumann G, Pausova Z, Elsabbagh M, Almasy L, Glahn DC, Bourgeron T, Labbe A, Paus T, Mottron L, Greenwood CMT, Huguet G, Jacquemont S. Effect Sizes of Deletions and Duplications on Autism Risk Across the Genome. Am J Psychiatry. 2021 Jan 1;178(1):87-98. doi: 10.1176/appi.ajp.2020.19080834. Epub 2020 Sep 11. PMID: 32911998; PMCID: PMC8931740.

189: Sahly AN, Krochmalnek E, St-Onge J, Srour M, Myers KA. Severe DNM1 encephalopathy with dysmyelination due to recurrent splice site pathogenic variant. Hum Genet. 2020 Dec;139(12):1575-1578. doi: 10.1007/s00439-020-02224-5. Epub 2020 Sep 9. PMID: 32909139.

190: Rezk A, Li R, Bar-Or A. Multiplexed detection and isolation of viable low- frequency cytokine-secreting human B cells using cytokine secretion assay and flow cytometry (CSA-Flow). Sci Rep. 2020 Sep 9;10(1):14823. doi: 10.1038/s41598-020-71750-z. PMID: 32908164; PMCID: PMC7481209.

191: Smith EE, Couillard P, Fisk JD, Ismail Z, Montero-Odasso M, Robillard JM, Vedel I, Sivananthan S, Gauthier S. Pandemic Dementia Scarce Resource Allocation. Can Geriatr J. 2020 Sep 1;23(3):216-218. doi: 10.5770/cgj.23.457. PMID: 32904792; PMCID: PMC7458602.

192: Zha C, Farah CA, Holt RJ, Ceroni F, Al-Abdi L, Thuriot F, Khan AO, Helaby R, Lévesque S, Alkuraya FS, Kraus A, Ragge NK, Sossin WS. Biallelic variants in the small optic lobe calpain CAPN15 are associated with congenital eye anomalies, deafness and other neurodevelopmental deficits. Hum Mol Genet. 2020 Nov 4;29(18):3054-3063. doi: 10.1093/hmg/ddaa198. PMID: 32885237; PMCID: PMC7645705.

193: Beauregard-Lacroix E, Pacheco-Cuellar G, Ajeawung NF, Tardif J, Dieterich K, Dabir T, Vind-Kezunovic D, White SM, Zadori D, Castiglioni C, Tranebjærg L, Tørring PM, Blair E, Wisniewska M, Camurri MV, van Bever Y, Molidperee S, Taylor J, Dionne-Laporte A, Sisodiya SM, Hennekam RCM, Campeau PM. DOORS syndrome and a recurrent truncating ATP6V1B2 variant. Genet Med. 2021 Jan;23(1):149-154. doi: 10.1038/s41436-020-00950-9. Epub 2020 Sep 2. Erratum in: Genet Med. 2020 Sep 15;: PMID: 32873933.

194: Chivukula S, Modiri O, Kashanian A, Babayan D, Ibrahim GM, Weil AG, Tu A, Wu JY, Mathern GW, Fallah A. Effect of Gene Mutation on Seizures in Surgery for Tuberous Sclerosis Complex. Can J Neurol Sci. 2021 May;48(3):327-334. doi: 10.1017/cjn.2020.185. Epub 2020 Aug 28. PMID: 32854808.

195: Oskoui M, Ng P, Zaman M, Buckley D, Kirton A, van Rensburg E, Wood E, Shevell M, Majnemer A. Complementary and Alternative Therapy Use in Children with Cerebral Palsy. Can J Neurol Sci. 2021 May;48(3):408-414. doi: 10.1017/cjn.2020.188. Epub 2020 Aug 28. PMID: 32854793.

196: Moreau JT, Baillet S, Dudley RW. Biased intelligence: on the subjectivity of digital objectivity. BMJ Health Care Inform. 2020 Aug;27(3):e100146. doi: 10.1136/bmjhci-2020-100146. PMID: 32830107; PMCID: PMC7445351.

197: Hatton SN, Huynh KH, Bonilha L, Abela E, Alhusaini S, Altmann A, Alvim MKM, Balachandra AR, Bartolini E, Bender B, Bernasconi N, Bernasconi A, Bernhardt B, Bargallo N, Caldairou B, Caligiuri ME, Carr SJA, Cavalleri GL, Cendes F, Concha L, Davoodi-Bojd E, Desmond PM, Devinsky O, Doherty CP, Domin M, Duncan JS, Focke NK, Foley SF, Gambardella A, Gleichgerrcht E, Guerrini R, Hamandi K, Ishikawa A, Keller SS, Kochunov PV, Kotikalapudi R, Kreilkamp BAK, Kwan P, Labate A, Langner S, Lenge M, Liu M, Lui E, Martin P, Mascalchi M, Moreira JCV, Morita-Sherman ME, O'Brien TJ, Pardoe HR, Pariente JC, Ribeiro LF, Richardson MP, Rocha CS, Rodríguez-Cruces R, Rosenow F, Severino M, Sinclair B, Soltanian-Zadeh H, Striano P, Taylor PN, Thomas RH, Tortora D, Velakoulis D, Vezzani A, Vivash L, von Podewils F, Vos SB, Weber B, Winston GP, Yasuda CL, Zhu AH, Thompson PM, Whelan CD, Jahanshad N, Sisodiya SM, McDonald CR. White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study. Brain. 2020 Aug 1;143(8):2454-2473. doi: 10.1093/brain/awaa200. PMID: 32814957; PMCID: PMC7567169.

198: Canadian Society of Clinical Neurophysiologists (CSCN); Canadian Association of Electroneurophysiology Technologists (CAET); Association of Electromyography Technologists of Canada (AETC); Board of Registration of Electromyography Technologists of Canada (BRETC), Canadian Board of Registration of Electroencephalograph Technologists (CBRET), Appendino JP, Baker SK, Chapman KM, Dykstra T, Hussein T, Jones ML, Mezei MM, Mirsattari SM, Ng M, Nikkel J, Obradovic V, Phan C, Robinson L, Scott A, Tellez-Zenteno J, Van Niekerk M, Venance S, Moore F. Practice Guidelines for Canadian Neurophysiology Laboratories During the COVID-19 Pandemic. Can J Neurol Sci. 2021 Jan;48(1):25-30. doi: 10.1017/cjn.2020.184. Epub 2020 Aug 19. PMID: 32811585; PMCID: PMC7578631.

199: Boychuck Z, Andersen J, Bussières A, Fehlings D, Kirton A, Li P, Oskoui M, Rodriguez C, Shevell M, Snider L, Majnemer A; PROMPT Group. Use of consensus methods to determine the early clinical signs of cerebral palsy. Paediatr Child Health. 2020 Aug;25(5):300-307. doi: 10.1093/pch/pxz061. Epub 2019 May 8. PMID: 32765166; PMCID: PMC7395325.

200: Hwang P, Hechtman L, Carboni-Jiménez A, Demchenko I, Maduro A, Mady N, Tounkara F, Sapkota RP, Brunet A. In Response to “Clinical Characteristics Associated with Early Phase Psychosis and Comorbid Substance Use”: Methodological Concerns. Can J Psychiatry. 2021 Feb;66(2):183-184. doi: 10.1177/0706743720947636. Epub 2020 Aug 7. PMID: 32762339; PMCID: PMC7918869.

201: Greer DM, Shemie SD, Lewis A, Torrance S, Varelas P, Goldenberg FD, Bernat JL, Souter M, Topcuoglu MA, Alexandrov AW, Baldisseri M, Bleck T, Citerio G, Dawson R, Hoppe A, Jacobe S, Manara A, Nakagawa TA, Pope TM, Silvester W, Thomson D, Al Rahma H, Badenes R, Baker AJ, Cerny V, Chang C, Chang TR, Gnedovskaya E, Han MK, Honeybul S, Jimenez E, Kuroda Y, Liu G, Mallick UK, Marquevich V, Mejia-Mantilla J, Piradov M, Quayyum S, Shrestha GS, Su YY, Timmons SD, Teitelbaum J, Videtta W, Zirpe K, Sung G. Determination of Brain Death/Death by Neurologic Criteria: The World Brain Death Project. JAMA. 2020 Sep 15;324(11):1078-1097. doi: 10.1001/jama.2020.11586. PMID: 32761206.

202: Schneeberger PE, Kortüm F, Korenke GC, Alawi M, Santer R, Woidy M, Buhas D, Fox S, Juusola J, Alfadhel M, Webb BD, Coci EG, Abou Jamra R, Siekmeyer M, Biskup S, Heller C, Maier EM, Javaher-Haghighi P, Bedeschi MF, Ajmone PF, Iascone M, Peeters H, Ballon K, Jaeken J, Rodríguez Alonso A, Palomares-Bralo M, Santos-Simarro F, Meuwissen MEC, Beysen D, Kooy RF, Houlden H, Murphy D, Doosti M, Karimiani EG, Mojarrad M, Maroofian R, Noskova L, Kmoch S, Honzik T, Cope H, Sanchez-Valle A; Undiagnosed Diseases Network, Gelb BD, Kurth I, Hempel M, Kutsche K. Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder. Brain. 2020 Aug 1;143(8):2437-2453. doi: 10.1093/brain/awaa204. PMID: 32761064; PMCID: PMC7447524.

203: Bis-Brewer DM, Gan-Or Z, Sleiman P; Inherited Neuropathy Consortium, Hakonarson H, Fazal S, Courel S, Cintra V, Tao F, Estiar MA, Tarnopolsky M, Boycott KM, Yoon G, Suchowersky O, Dupré N, Cheng A, Lloyd TE, Rouleau G, Schüle R, Züchner S. Assessing non-Mendelian inheritance in inherited axonopathies. Genet Med. 2020 Dec;22(12):2114-2119. doi: 10.1038/s41436-020-0924-0. Epub 2020 Aug 3. PMID: 32741968; PMCID: PMC7710562.

204: Dermer E, Spahr A, Tran LT, Mirchi A, Pelletier F, Guerrero K, Ahmed S, Brais B, Braverman N, Buhas D, Chandratre S, Chenier S, Chrestian N, Desmeules M, Dilenge ME, Laflamme J, Larbrisseau A, Legault G, Lim KY, Maftei C, Major P, Malvey-Dorn E, Marois P, Mitchell J, Nadeau A, Osterman B, Paradis I, Pohl D, Reggin J, Riou E, Roedde G, Rossignol E, Sébire G, Shevell M, Srour M, Sylvain M, Tarnopolsky M, Venkateswaran S, Sullivan M, Bernard G. Stress in Parents of Children With Genetically Determined Leukoencephalopathies: A Pilot Study. J Child Neurol. 2020 Nov;35(13):901-907. doi: 10.1177/0883073820938645. Epub 2020 Jul 28. PMID: 32720856.

205: Al Amrani F, Racine E, Shevell M, Wintermark P. Death after Birth Asphyxia in the Cooling Era. J Pediatr. 2020 Nov;226:289-293. doi: 10.1016/j.jpeds.2020.07.041. Epub 2020 Jul 16. PMID: 32682749.

206: Lewis A, Liebman J, Kreiger-Benson E, Kumpfbeck A, Bakkar A, Shemie SD, Sung G, Torrance S, Greer D. Ancillary Testing for Determination of Death by Neurologic Criteria Around the World. Neurocrit Care. 2021 Apr;34(2):473-484. doi: 10.1007/s12028-020-01039-6. PMID: 32648194.

207: Fortin O, Ashour M, Lacroix C, Sabapathy CA, Myers KA. Megalencephaly- Capillary Malformation-Polymicrogyria with Cerebral Venous Thrombosis. Can J Neurol Sci. 2020 Nov;47(6):828-829. doi: 10.1017/cjn.2020.127. Epub 2020 Jun 23. PMID: 32631464.

208: Healey A, Leeies M, Hrymak C, Chochinov A, Grunau B, Paunovic B, Teitelbaum J, Wilson LC, Shemie SD. CAEP Position Statement - Management of devastating brain injuries in the emergency department: Enhancing neuroprognostication and maintaining the opportunity for organ and tissue donation. CJEM. 2020 Sep;22(5):658-660. doi: 10.1017/cem.2020.357. Erratum in: CJEM. 2020 Sep;22(5):E9. PMID: 32618532; PMCID: PMC7509745.

209: Mirchi A, Saint-Martin C, Myers KA. Spontaneous Multilevel Cerebrospinal Fluid Leak in Marfan Syndrome. Ann Neurol. 2020 Oct;88(4):855-856. doi: 10.1002/ana.25837. Epub 2020 Jul 14. PMID: 32613612.

210: Fortin O, Vincelette C, Chénier S, Ghais A, Shevell MI, Simard-Tremblay E, Myers KA. Copy number variation in genetic epilepsy with febrile seizures plus. Eur J Paediatr Neurol. 2020 Jul;27:111-115. doi: 10.1016/j.ejpn.2020.05.005. Epub 2020 Jun 20. PMID: 32595013.

211: Jenkins DJA, Jayalath VH, Choo VL, Viguiliouk E, Kendall CWC, Srichaikul K, Mirrahimi A, Bernstein CN, Chang TM, Gold P, Haynes RB, Hollenberg MD, Lozano AM, Posner BI, Ronald AR, Vranic M, Wang YT, Chiavaroli L, de Souza RJ, Nishi S, Pichika SC, Gillett C, Tsirakis T, Sievenpiper JL. Does conventional early life academic excellence predict later life scientific discovery? An assessment of the lives of great medical innovators. QJM. 2021 Oct 7;114(6):381-389. doi: 10.1093/qjmed/hcaa210. PMID: 32589722; PMCID: PMC8497073.

212: Perrier S, Gauquelin L, Fallet-Bianco C, Dishop MK, Michell-Robinson MA, Tran LT, Guerrero K, Darbelli L, Srour M, Petrecca K, Renaud DL, Saito M, Cohen S, Leiz S, Alhaddad B, Haack TB, Tejera-Martin I, Monton FI, Rodriguez-Espinosa N, Pohl D, Nageswaran S, Grefe A, Glamuzina E, Bernard G. Expanding the phenotypic and molecular spectrum of RNA polymerase III-related leukodystrophy. Neurol Genet. 2020 May 11;6(3):e425. doi: 10.1212/NXG.0000000000000425. PMID: 32582862; PMCID: PMC7238899.

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258: Deng MY, Sill M, Sturm D, Stichel D, Witt H, Ecker J, Wittmann A, Schittenhelm J, Ebinger M, Schuhmann MU, Figarella-Branger D, Aronica E, Staszewski O, Preusser M, Haberler C, Lauten M, Schüller U, Hartmann C, Snuderl M, Dunham C, Jabado N, Wesseling P, Deckert M, Keyvani K, Gottardo N, Giangaspero F, von Hoff K, Ellison DW, Pietsch T, Herold-Mende C, Milde T, Witt O, Kool M, Korshunov A, Wick W, von Deimling A, Pfister SM, Jones DTW, Sahm F. Diffuse glioneuronal tumour with oligodendroglioma-like features and nuclear clusters (DGONC) - a molecularly defined glioneuronal CNS tumour class displaying recurrent monosomy 14. Neuropathol Appl Neurobiol. 2020 Aug;46(5):422-430. doi: 10.1111/nan.12590. Epub 2020 Feb 5. PMID: 31867747.

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260: Li BK, Vasiljevic A, Dufour C, Yao F, Ho BLB, Lu M, Hwang EI, Gururangan S, Hansford JR, Fouladi M, Nobusawa S, Laquerriere A, Delisle MB, Fangusaro J, Forest F, Toledano H, Solano-Paez P, Leary S, Birks D, Hoffman LM, Szathmari A, Faure-Conter C, Fan X, Catchpoole D, Zhou L, Schultz KAP, Ichimura K, Gauchotte G, Jabado N, Jones C, Loussouarn D, Mokhtari K, Rousseau A, Ziegler DS, Tanaka S, Pomeroy SL, Gajjar A, Ramaswamy V, Hawkins C, Grundy RG, Hill DA, Bouffet E, Huang A, Jouvet A. Pineoblastoma segregates into molecular sub-groups with distinct clinico-pathologic features: a Rare Brain Tumor Consortium registry study. Acta Neuropathol. 2020 Feb;139(2):223-241. doi: 10.1007/s00401-019-02111-y. Epub 2019 Dec 9. PMID: 31820118; PMCID: PMC7673644.

261: Mithani K, Boutet A, Germann J, Elias GJB, Weil AG, Shah A, Guillen M, Bernal B, Achua JK, Ragheb J, Donner E, Lozano AM, Widjaja E, Ibrahim GM. Lesion Network Localization of Seizure Freedom following MR-guided Laser Interstitial Thermal Ablation. Sci Rep. 2019 Dec 9;9(1):18598. doi: 10.1038/s41598-019-55015-y. PMID: 31819108; PMCID: PMC6901556.

262: Mendes MI, Green LMC, Bertini E, Tonduti D, Aiello C, Smith D, Salsano E, Beerepoot S, Hertecant J, von Spiczak S, Livingston JH, Emrick L, Fraser J, Russell L, Bernard G, Magri S, Di Bella D, Taroni F, Koenig MK, Moroni I, Cappuccio G, Brunetti-Pierri N, Rhee J, Mendelsohn BA, Helbig I, Helbig K, Muhle H, Ismayl O, Vanderver AL, Salomons GS, van der Knaap MS, Wolf NI. RARS1-related hypomyelinating leukodystrophy: Expanding the spectrum. Ann Clin Transl Neurol. 2020 Jan;7(1):83-93. doi: 10.1002/acn3.50960. Epub 2019 Dec 8. PMID: 31814314; PMCID: PMC6952319.

263: Le A, Yeganeh M, Buhas D, Trempe MJ, Myers KA. Monocarboxylate transporter-1 deficiency results in severe metabolic acidosis with ketogenic diet in early onset absence epilepsy: Case report. Seizure. 2020 Jan;74:31-32. doi: 10.1016/j.seizure.2019.11.008. Epub 2019 Nov 28. PMID: 31812089.

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271: Sievers P, Chiang J, Schrimpf D, Stichel D, Paramasivam N, Sill M, Gayden T, Casalini B, Reuss DE, Dalton J, Pajtler KW, Hänggi D, Herold-Mende C, Rushing E, Korshunov A, Mawrin C, Weller M, Schlesner M, Wick W, Jabado N, Jones DTW, Pfister SM, von Deimling A, Ellison DW, Sahm F. YAP1-fusions in pediatric NF2-wildtype meningioma. Acta Neuropathol. 2020 Jan;139(1):215-218. doi: 10.1007/s00401-019-02095-9. Epub 2019 Nov 16. PMID: 31734728.

272: Nalls MA, Blauwendraat C, Vallerga CL, Heilbron K, Bandres-Ciga S, Chang D, Tan M, Kia DA, Noyce AJ, Xue A, Bras J, Young E, von Coelln R, Simón-Sánchez J, Schulte C, Sharma M, Krohn L, Pihlstrøm L, Siitonen A, Iwaki H, Leonard H, Faghri F, Gibbs JR, Hernandez DG, Scholz SW, Botia JA, Martinez M, Corvol JC, Lesage S, Jankovic J, Shulman LM, Sutherland M, Tienari P, Majamaa K, Toft M, Andreassen OA, Bangale T, Brice A, Yang J, Gan-Or Z, Gasser T, Heutink P, Shulman JM, Wood NW, Hinds DA, Hardy JA, Morris HR, Gratten J, Visscher PM, Graham RR, Singleton AB; 23andMe Research Team; System Genomics of Parkinson's Disease Consortium; International Parkinson's Disease Genomics Consortium. Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies. Lancet Neurol. 2019 Dec;18(12):1091-1102. doi: 10.1016/S1474-4422(19)30320-5. PMID: 31701892; PMCID: PMC8422160.

273: Rtshiladze MA, Roy AA, Goltsman D, Hunt J, Reddy R, Gianoutsos MP. The removal of cranial springs used in the treatment of scaphocephaly: A minimal access approach. J Craniomaxillofac Surg. 2019 Nov;47(11):1706-1711. doi: 10.1016/j.jcms.2019.04.001. Epub 2019 Apr 16. PMID: 31677988.

274: Suzuki H, Kumar SA, Shuai S, Diaz-Navarro A, Gutierrez-Fernandez A, De Antonellis P, Cavalli FMG, Juraschka K, Farooq H, Shibahara I, Vladoiu MC, Zhang J, Abeysundara N, Przelicki D, Skowron P, Gauer N, Luu B, Daniels C, Wu X, Forget A, Momin A, Wang J, Dong W, Kim SK, Grajkowska WA, Jouvet A, Fèvre- Montange M, Garrè ML, Nageswara Rao AA, Giannini C, Kros JM, French PJ, Jabado N, Ng HK, Poon WS, Eberhart CG, Pollack IF, Olson JM, Weiss WA, Kumabe T, López- Aguilar E, Lach B, Massimino M, Van Meir EG, Rubin JB, Vibhakar R, Chambless LB, Kijima N, Klekner A, Bognár L, Chan JA, Faria CC, Ragoussis J, Pfister SM, Goldenberg A, Wechsler-Reya RJ, Bailey SD, Garzia L, Morrissy AS, Marra MA, Huang X, Malkin D, Ayrault O, Ramaswamy V, Puente XS, Calarco JA, Stein L, Taylor MD. Recurrent noncoding U1 snRNA mutations drive cryptic splicing in SHH medulloblastoma. Nature. 2019 Oct;574(7780):707-711. doi: 10.1038/s41586-019-1650-0. Epub 2019 Oct 9. PMID: 31664194; PMCID: PMC7141958.

275: Amrom D, Poduri A, Goldman JS, Dan B, Deconinck N, Pichon B, Nadaf J, Andermann F, Andermann E, Walsh CA, Dobyns WB. Duplication 2p16 is associated with perisylvian polymicrogyria. Am J Med Genet A. 2019 Dec;179(12):2343-2356. doi: 10.1002/ajmg.a.61342. Epub 2019 Oct 29. PMID: 31660690.

276: Smith ER, Concepcion TL, Shrime M, Niemeier K, Mohamed M, Dahir S, Ismail EA, Poenaru D, Rice HE; Global Initiative for Children’s Surgery. Waiting Too Long: The Contribution of Delayed Surgical Access to Pediatric Disease Burden in Somaliland. World J Surg. 2020 Mar;44(3):656-664. doi: 10.1007/s00268-019-05239-w. PMID: 31654200.

277: Stevelink R, Pangilinan F, Jansen FE, Braun KPJ; International League Against Epilepsy Consortium on Complex Epilepsies, Molloy AM, Brody LC, Koeleman BPC. Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsy. Mol Genet Metab Rep. 2019 Oct 11;21:100518. doi: 10.1016/j.ymgmr.2019.100518. PMID: 31641590; PMCID: PMC6796782.

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280: Burgess R, Wang S, McTague A, Boysen KE, Yang X, Zeng Q, Myers KA, Rochtus A, Trivisano M, Gill D; EIMFS Consortium, Sadleir LG, Specchio N, Guerrini R, Marini C, Zhang YH, Mefford HC, Kurian MA, Poduri AH, Scheffer IE. The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures. Ann Neurol. 2019 Dec;86(6):821-831. doi: 10.1002/ana.25619. Erratum in: Ann Neurol. 2020 Apr;87(4):658. PMID: 31618474; PMCID: PMC7423163.

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283: Ademuyiwa AO, Odugbemi TO, Bode CO, Elebute OA, Alakaloko FM, Alabi EO, Bankole O, Ladipo-Ajayi O, Seyi-Olajide JO, Okusanya B, Abazie O, Ademuyiwa IY, Onwuka A, Tran T, Makanjuola A, Gupta S, Ots R, Harrison EM, Poenaru D, Nwomeh BC. Prevalence of surgically correctable conditions among children in a mixed urban-rural community in Nigeria using the SOSAS survey tool: Implications for paediatric surgical capacity-building. PLoS One. 2019 Oct 10;14(10):e0223423. doi: 10.1371/journal.pone.0223423. PMID: 31600252; PMCID: PMC6786634.

284: Wheelwright M, Selvey PJ, Steinbok P, Singhal A, Ibrahim G, Fallah A, Weil AG, Halvorson K, Tu A. Systematic review of spinal deformities following multi- level selective dorsal rhizotomy. Childs Nerv Syst. 2020 May;36(5):1025-1035. doi: 10.1007/s00381-019-04375-x. Epub 2019 Oct 8. PMID: 31595313.

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293: Shevell M. Health Professional Burnout: An (Un)Ethical Consequence of Modern Health Care? Can J Neurol Sci. 2019 Nov;46(6):682-683. doi: 10.1017/cjn.2019.280. PMID: 31500677.

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385: Mirchi A, Pelletier F, Tran LT, Keller S, Braverman N, Tonduti D, Vanderver A, Pizzino A, Dilenge ME, Poulin C, Shevell M, Majnemer A, Sébire G, Srour M, Osterman B, Boucher RM, Vanasse M, Rossignol E, Mitchell J, Venkateswaran S, Pohl D, Kauffman M, Schiffmann R, Goizet C, Moutton S, Roncarolo F, Bernard G. Health-Related Quality of Life for Patients With Genetically Determined Leukoencephalopathy. Pediatr Neurol. 2018 Jul;84:21-26. doi: 10.1016/j.pediatrneurol.2018.03.015. Epub 2018 Apr 9. PMID: 29859719.

386: Maranzano J, Till C, Assemlal HE, Fonov V, Brown R, Araujo D, O'Mahony J, Yeh EA, Bar-Or A, Marrie RA, Collins L, Banwell B, Arnold DL, Narayanan S. Detection and clinical correlation of leukocortical lesions in pediatric-onset multiple sclerosis on multi-contrast MRI. Mult Scler. 2019 Jun;25(7):980-986. doi: 10.1177/1352458518779952. Epub 2018 Jun 1. PMID: 29852831.

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388: Schur S, Allen V, White A, Mirsky D, Stence N, O'Neill B, Handler M, Dudley R, Laoprasert P. Significance of FDG-PET Hypermetabolism in Children with Intractable Focal Epilepsy. Pediatr Neurosurg. 2018;53(3):153-162. doi: 10.1159/000487088. Epub 2018 Apr 19. PMID: 29672310.

389: Schneider RE, Ng P, Zhang X, Andersen J, Buckley D, Fehlings D, Kirton A, Wood E, van Rensburg E, Shevell MI, Oskoui M. The Association Between Maternal Age and Cerebral Palsy Risk Factors. Pediatr Neurol. 2018 May;82:25-28. doi: 10.1016/j.pediatrneurol.2018.01.005. Epub 2018 Feb 12. PMID: 29622489.

390: Alawadhi A, Saint-Martin C, Bhanji F, Srour M, Atkinson J, Sébire G. Acute Hemorrhagic Encephalitis Responding to Combined Decompressive Craniectomy, Intravenous Immunoglobulin, and Corticosteroid Therapies: Association with Novel RANBP2 Variant. Front Neurol. 2018 Mar 12;9:130. doi: 10.3389/fneur.2018.00130. PMID: 29593631; PMCID: PMC5857578.

391: Cooper YA, Pianka ST, Alotaibi NM, Babayan D, Salavati B, Weil AG, Ibrahim GM, Wang AC, Fallah A. Repetitive transcranial magnetic stimulation for the treatment of drug-resistant epilepsy: A systematic review and individual participant data meta-analysis of real-world evidence. Epilepsia Open. 2017 Dec 27;3(1):55-65. doi: 10.1002/epi4.12092. PMID: 29588988; PMCID: PMC5839309.

392: Mendes MI, Gutierrez Salazar M, Guerrero K, Thiffault I, Salomons GS, Gauquelin L, Tran LT, Forget D, Gauthier MS, Waisfisz Q, Smith DEC, Simons C, van der Knaap MS, Marquardt I, Lemes A, Mierzewska H, Weschke B, Koehler W, Coulombe B, Wolf NI, Bernard G. Bi-allelic Mutations in EPRS, Encoding the Glutamyl-Prolyl-Aminoacyl-tRNA Synthetase, Cause a Hypomyelinating Leukodystrophy. Am J Hum Genet. 2018 Apr 5;102(4):676-684. doi: 10.1016/j.ajhg.2018.02.011. Epub 2018 Mar 22. PMID: 29576217; PMCID: PMC5985283.

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463: Vezina N, Al-Halabi B, Shash H, Dudley RR, Gilardino MS. A Review of Techniques Used in the Management of Growing Skull Fractures. J Craniofac Surg. 2017 May;28(3):604-609. doi: 10.1097/SCS.0000000000003379. PMID: 28060103.

464: Nguyen TV, Lew J, Albaugh MD, Botteron KN, Hudziak JJ, Fonov VS, Collins DL, Ducharme S, McCracken JT. Sex-specific associations of testosterone with prefrontal-hippocampal development and executive function. Psychoneuroendocrinology. 2017 Feb;76:206-217. doi: 10.1016/j.psyneuen.2016.12.005. Epub 2016 Dec 8. PMID: 27984812; PMCID: PMC5272813.

465: Weil AG, Wang AC, Westwick HJ, Ibrahim GM, Ariani RT, Crevier L, Perreault S, Davidson T, Tseng CH, Fallah A. Survival in pediatric medulloblastoma: a population-based observational study to improve prognostication. J Neurooncol. 2017 Mar;132(1):99-107. doi: 10.1007/s11060-016-2341-4. Epub 2016 Dec 15. PMID: 27981412.

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467: Chrestian N, Dupré N, Gan-Or Z, Szuto A, Chen S, Venkitachalam A, Brisson JD, Warman-Chardon J, Ahmed S, Ashtiani S, MacDonald H, Mohsin N, Mourabit-Amari K, Provencher P, Boycott KM, Stavropoulos DJ, Dion PA, Ray PN, Suchowersky O, Rouleau GA, Yoon G. Clinical and genetic study of hereditary spastic paraplegia in Canada. Neurol Genet. 2016 Dec 5;3(1):e122. doi: 10.1212/NXG.0000000000000122. PMID: 27957547; PMCID: PMC5141523.

468: Foveau B, Albrecht S, Bennett DA, Correa JA, LeBlanc AC. Increased Caspase-6 activity in the human anterior olfactory nuclei of the olfactory bulb is associated with cognitive impairment. Acta Neuropathol Commun. 2016 Dec 8;4(1):127. doi: 10.1186/s40478-016-0400-x. PMID: 27931265; PMCID: PMC5146837.

469: Trickey K, Hornby L, Shemie SD, Teitelbaum J. Mechanism of Death after Decompressive Craniectomy in Non-Traumatic Brain Injury. Can J Neurol Sci. 2017 Jan;44(1):112-115. doi: 10.1017/cjn.2016.320. Epub 2016 Dec 5. PMID: 27917726.

470: Xue D, Kaufman GN, Dembele M, Beland M, Massoud AH, Mindt BC, Fiter R, Fixman ED, Martin JG, Friedel RH, Divangahi M, Fritz JH, Mazer BD. Semaphorin 4C Protects against Allergic Inflammation: Requirement of Regulatory CD138+ Plasma Cells. J Immunol. 2017 Jan 1;198(1):71-81. doi: 10.4049/jimmunol.1600831. Epub 2016 Nov 23. PMID: 27881703.

471: Burstein B, Fauteux-Lamarre E, Cheng A, Chalut D, Bretholz A. Simulation and Web-based learning increases utilization of Bier block for forearm fracture reduction in the pediatric emergency department. CJEM. 2017 Nov;19(6):434-440. doi: 10.1017/cem.2016.392. Epub 2016 Nov 21. PMID: 27866507.

472: Ulrick N, Goldstein A, Simons C, Taft RJ, Helman G, Pizzino A, Bloom M, Vogt J, Pysden K, Diodato D, Martinelli D, Monavari A, Buhas D, van Karnebeek CD, Dorboz I, Boespflug-Tanguy O, Rodriguez D, Tétreault M, Majewski J, Bernard G, Ng YS; Care4Rare Canada Consortium, McFarland R, Vanderver A. RMND1-Related Leukoencephalopathy With Temporal Lobe Cysts and Hearing Loss-Another Mendelian Mimicker of Congenital Cytomegalovirus Infection. Pediatr Neurol. 2017 Jan;66:59-62. doi: 10.1016/j.pediatrneurol.2016.09.003. Epub 2016 Sep 13. PMID: 27843092.

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477: Garzon MC, Epstein LG, Heyer GL, Frommelt PC, Orbach DB, Baylis AL, Blei F, Burrows PE, Chamlin SL, Chun RH, Hess CP, Joachim S, Johnson K, Kim W, Liang MG, Maheshwari M, McCoy GN, Metry DW, Monrad PA, Pope E, Powell J, Shwayder TA, Siegel DH, Tollefson MM, Vadivelu S, Lew SM, Frieden IJ, Drolet BA. PHACE Syndrome: Consensus-Derived Diagnosis and Care Recommendations. J Pediatr. 2016 Nov;178:24-33.e2. doi: 10.1016/j.jpeds.2016.07.054. Epub 2016 Sep 19. PMID: 27659028; PMCID: PMC6599593.

478: Warsi NM, Lasry O, Farah A, Saint-Martin C, Montes JL, Atkinson J, Farmer JP, Dudley RW. 3-T intraoperative MRI (iMRI) for pediatric epilepsy surgery. Childs Nerv Syst. 2016 Dec;32(12):2415-2422. doi: 10.1007/s00381-016-3263-3. Epub 2016 Oct 18. PMID: 27757571.

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480: Jayakar P, Gotman J, Harvey AS, Palmini A, Tassi L, Schomer D, Dubeau F, Bartolomei F, Yu A, Kršek P, Velis D, Kahane P. Diagnostic utility of invasive EEG for epilepsy surgery: Indications, modalities, and techniques. Epilepsia. 2016 Nov;57(11):1735-1747. doi: 10.1111/epi.13515. Epub 2016 Sep 28. PMID: 27677490.

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483: Aljared T, Farmer JP, Tampieri D. Feasibility and value of preoperative embolization of a congenital choroid plexus tumour in the premature infant: An illustrative case report with technical details. Interv Neuroradiol. 2016 Dec;22(6):732-735. doi: 10.1177/1591019916665346. Epub 2016 Sep 7. PMID: 27605545; PMCID: PMC5564368.

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488: Dudley RW, Torok MR, Hoffman L, Levy JM, Handler MH, Liu AK, Hankinson TC. Response to Journal Club: Pediatric Low-Grade Ganglioglioma: Epidemiology, Treatments, and Outcome Analysis of 348 Children From the Surveillance, Epidemiology, and End Results Database. Neurosurgery. 2016 Aug;79(2):309. doi: 10.1227/NEU.0000000000001275. PMID: 27428632.

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505: Shao YH, Choquet K, La Piana R, Tétreault M, Dicaire MJ; Care4Rare Canada Consortium, Boycott KM, Majewski J, Brais B. Mutations in GALC cause late-onset Krabbe disease with predominant cerebellar ataxia. Neurogenetics. 2016 Apr;17(2):137-41. doi: 10.1007/s10048-016-0476-2. Epub 2016 Feb 26. PMID: 26915362.

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566: Gilardino MS, Karunanayake M, Al-Humsi T, Izadpanah A, Al-Ajmi H, Marcoux J, Atkinson J, Farmer JP. A comparison and cost analysis of cranioplasty techniques: autologous bone versus custom computer-generated implants. J Craniofac Surg. 2015 Jan;26(1):113-7. doi: 10.1097/SCS.0000000000001305. PMID: 25534061.

567: Ahn JJ, O'Mahony J, Moshkova M, Hanwell HE, Singh H, Zhang MA, Marrie RA, Bar-Or A, Sadovnick DA, Dunn SE, Banwell BL. Puberty in females enhances the risk of an outcome of multiple sclerosis in children and the development of central nervous system autoimmunity in mice. Mult Scler. 2015 May;21(6):735-48. doi: 10.1177/1352458514551453. Epub 2014 Dec 22. PMID: 25533291.

568: Pinchefsky E, Dubrovsky AS, Friedman D, Shevell M. Part II–Management of pediatric post-traumatic headaches. Pediatr Neurol. 2015 Mar;52(3):270-80. doi: 10.1016/j.pediatrneurol.2014.10.015. Epub 2014 Oct 16. PMID: 25499091.

569: Dai YE, Tang L, Healy J, Sinnett D. Contribution of polymorphisms in IKZF1 gene to childhood acute leukemia: a meta-analysis of 33 case-control studies. PLoS One. 2014 Nov 25;9(11):e113748. doi: 10.1371/journal.pone.0113748. PMID: 25423013; PMCID: PMC4244140.

570: La Piana R, Vanasse M, Brais B, Bernard G. Myelination Delay and Allan- Herndon-Dudley Syndrome Caused by a Novel Mutation in the SLC16A2 Gene. J Child Neurol. 2015 Sep;30(10):1371-4. doi: 10.1177/0883073814555189. Epub 2014 Nov 7. PMID: 25380603.

571: La Piana R, Tran LT, Guerrero K, Brais B, Levesque S, Sébire G, Riou E, Bernard G. Spastic paraparesis and marked improvement of leukoencephalopathy in Aicardi-Goutières syndrome. Neuropediatrics. 2014 Dec;45(6):406-10. doi: 10.1055/s-0034-1393710. Epub 2014 Oct 24. PMID: 25343331.

572: Wolf NI, Vanderver A, van Spaendonk RM, Schiffmann R, Brais B, Bugiani M, Sistermans E, Catsman-Berrevoets C, Kros JM, Pinto PS, Pohl D, Tirupathi S, Strømme P, de Grauw T, Fribourg S, Demos M, Pizzino A, Naidu S, Guerrero K, van der Knaap MS, Bernard G; 4H Research Group. Clinical spectrum of 4H leukodystrophy caused by POLR3A and POLR3B mutations. Neurology. 2014 Nov 18;83(21):1898-905. doi: 10.1212/WNL.0000000000001002. Epub 2014 Oct 22. PMID: 25339210; PMCID: PMC4248461.

573: Winkler-Schwartz A, Garfinkle J, Shevell MI. Autism spectrum disorder in a term birth neonatal intensive care unit population. Pediatr Neurol. 2014 Dec;51(6):776-80. doi: 10.1016/j.pediatrneurol.2014.07.009. Epub 2014 Jul 16. PMID: 25303867.

574: Donald KA, Kakooza AM, Wammanda RD, Mallewa M, Samia P, Babakir H, Bearden D, Majnemer A, Fehlings D, Shevell M, Chugani H, Wilmshurst JM. Pediatric Cerebral Palsy in Africa: Where Are We? J Child Neurol. 2015 Jul;30(8):963-71. doi: 10.1177/0883073814549245. Epub 2014 Oct 7. PMID: 25296926.

575: Armstrong-Wells J, Donnelly M, Post MD, Manco-Johnson MJ, Winn VD, Sébire G. Inflammatory predictors of neurologic disability after preterm premature rupture of membranes. Am J Obstet Gynecol. 2015 Feb;212(2):212.e1-9. doi: 10.1016/j.ajog.2014.09.016. Epub 2014 Sep 16. PMID: 25223243; PMCID: PMC4312536.

576: Jamuar SS, Lam AT, Kircher M, D'Gama AM, Wang J, Barry BJ, Zhang X, Hill RS, Partlow JN, Rozzo A, Servattalab S, Mehta BK, Topcu M, Amrom D, Andermann E, Dan B, Parrini E, Guerrini R, Scheffer IE, Berkovic SF, Leventer RJ, Shen Y, Wu BL, Barkovich AJ, Sahin M, Chang BS, Bamshad M, Nickerson DA, Shendure J, Poduri A, Yu TW, Walsh CA. Somatic mutations in cerebral cortical malformations. N Engl J Med. 2014 Aug 21;371(8):733-43. doi: 10.1056/NEJMoa1314432. PMID: 25140959; PMCID: PMC4274952.

577: Finkel RS, McDermott MP, Kaufmann P, Darras BT, Chung WK, Sproule DM, Kang PB, Foley AR, Yang ML, Martens WB, Oskoui M, Glanzman AM, Flickinger J, Montes J, Dunaway S, O'Hagen J, Quigley J, Riley S, Benton M, Ryan PA, Montgomery M, Marra J, Gooch C, De Vivo DC. Observational study of spinal muscular atrophy type I and implications for clinical trials. Neurology. 2014 Aug 26;83(9):810-7. doi: 10.1212/WNL.0000000000000741. Epub 2014 Jul 30. PMID: 25080519; PMCID: PMC4155049.

578: Robinson MÈ, Rossignol E, Brais B, Rouleau G, Arbour JF, Bernard G. Vanishing white matter disease in French-Canadian patients from Quebec. Pediatr Neurol. 2014 Aug;51(2):225-32. doi: 10.1016/j.pediatrneurol.2014.05.006. Epub 2014 May 14. PMID: 25079571.

579: Fasano A, Bologna M, Iezzi E, Pavone L, Srour M, Di Biasio F, Grillea G, Rouleau GA, Levert A, Sebastiano F, Colonnese C, Berardelli A. Congenital Mirror Movements in a New Italian Family. Mov Disord Clin Pract. 2014 Jul 28;1(3):180-187. doi: 10.1002/mdc3.12066. PMID: 30713853; PMCID: PMC6353446.

580: Gauvin M, Lina JM, Lachapelle P. Advance in ERG analysis: from peak time and amplitude to frequency, power, and energy. Biomed Res Int. 2014;2014:246096. doi: 10.1155/2014/246096. Epub 2014 Jul 1. PMID: 25061605; PMCID: PMC4100345.

581: Zhang JY, Oskoui M, Shevell M. A population-based study of communication impairment in cerebral palsy. J Child Neurol. 2015 Mar;30(3):277-84. doi: 10.1177/0883073814538497. Epub 2014 Jul 22. PMID: 25051968.

582: Koenekoop RK, Sui R, Sallum J, van den Born LI, Ajlan R, Khan A, den Hollander AI, Cremers FP, Mendola JD, Bittner AK, Dagnelie G, Schuchard RA, Saperstein DA. Oral 9-cis retinoid for childhood blindness due to Leber congenital amaurosis caused by RPE65 or LRAT mutations: an open-label phase 1b trial. Lancet. 2014 Oct 25;384(9953):1513-20. doi: 10.1016/S0140-6736(14)60153-7. Epub 2014 Jul 13. PMID: 25030840.

583: Zeidman LA, Ziller MG, Shevell M. Gerstmann, Sträussler, and Scheinker: the persecution of the men behind the syndrome. Neurology. 2014 Jul 15;83(3):272-7. doi: 10.1212/WNL.0000000000000606. PMID: 25024443.

584: Kashani A, Thiffault I, Dilenge ME, Saint-Martin C, Guerrero K, Tran LT, Shoubridge E, van der Knaap MS, Braverman N, Bernard G. A homozygous mutation in the NDUFS1 gene presents with a mild cavitating leukoencephalopathy. Neurogenetics. 2014 Aug;15(3):161-4. doi: 10.1007/s10048-014-0412-2. Epub 2014 Jun 21. PMID: 24952175.

585: Kahle KT, Merner ND, Friedel P, Silayeva L, Liang B, Khanna A, Shang Y, Lachance-Touchette P, Bourassa C, Levert A, Dion PA, Walcott B, Spiegelman D, Dionne-Laporte A, Hodgkinson A, Awadalla P, Nikbakht H, Majewski J, Cossette P, Deeb TZ, Moss SJ, Medina I, Rouleau GA. Genetically encoded impairment of neuronal KCC2 cotransporter function in human idiopathic generalized epilepsy. EMBO Rep. 2014 Jul;15(7):766-74. doi: 10.15252/embr.201438840. Epub 2014 Jun 13. PMID: 24928908; PMCID: PMC4196980.

586: Vargus-Adams JN, Majnemer A. International Classification of Functioning, Disability and Health (ICF) as a framework for change: revolutionizing rehabilitation. J Child Neurol. 2014 Aug;29(8):1030-5. doi: 10.1177/0883073814533595. Epub 2014 May 21. PMID: 24850572.

587: Perreault S, Ramaswamy V, Achrol AS, Chao K, Liu TT, Shih D, Remke M, Schubert S, Bouffet E, Fisher PG, Partap S, Vogel H, Taylor MD, Cho YJ, Yeom KW. MRI surrogates for molecular subgroups of medulloblastoma. AJNR Am J Neuroradiol. 2014 Jul;35(7):1263-9. doi: 10.3174/ajnr.A3990. Epub 2014 May 15. PMID: 24831600; PMCID: PMC4819007.

588: Jadavji NM, Bahous RH, Deng L, Malysheva O, Grand'maison M, Bedell BJ, Caudill MA, Rozen R. Mouse model for deficiency of methionine synthase reductase exhibits short-term memory impairment and disturbances in brain choline metabolism. Biochem J. 2014 Jul 15;461(2):205-12. doi: 10.1042/BJ20131568. PMID: 24800750.

589: Fontebasso AM, Papillon-Cavanagh S, Schwartzentruber J, Nikbakht H, Gerges N, Fiset PO, Bechet D, Faury D, De Jay N, Ramkissoon LA, Corcoran A, Jones DT, Sturm D, Johann P, Tomita T, Goldman S, Nagib M, Bendel A, Goumnerova L, Bowers DC, Leonard JR, Rubin JB, Alden T, Browd S, Geyer JR, Leary S, Jallo G, Cohen K, Gupta N, Prados MD, Carret AS, Ellezam B, Crevier L, Klekner A, Bognar L, Hauser P, Garami M, Myseros J, Dong Z, Siegel PM, Malkin H, Ligon AH, Albrecht S, Pfister SM, Ligon KL, Majewski J, Jabado N, Kieran MW. Recurrent somatic mutations in ACVR1 in pediatric midline high-grade astrocytoma. Nat Genet. 2014 May;46(5):462-6. doi: 10.1038/ng.2950. Epub 2014 Apr 6. PMID: 24705250; PMCID: PMC4282994.

590: Dubrovsky AS, Friedman D, Kocilowicz H. Pediatric post-traumatic headaches and peripheral nerve blocks of the scalp: a case series and patient satisfaction survey. Headache. 2014 May;54(5):878-87. doi: 10.1111/head.12334. Epub 2014 Apr 2. PMID: 24697265.

591: Kool M, Jones DT, Jäger N, Northcott PA, Pugh TJ, Hovestadt V, Piro RM, Esparza LA, Markant SL, Remke M, Milde T, Bourdeaut F, Ryzhova M, Sturm D, Pfaff E, Stark S, Hutter S, Seker-Cin H, Johann P, Bender S, Schmidt C, Rausch T, Shih D, Reimand J, Sieber L, Wittmann A, Linke L, Witt H, Weber UD, Zapatka M, König R, Beroukhim R, Bergthold G, van Sluis P, Volckmann R, Koster J, Versteeg R, Schmidt S, Wolf S, Lawerenz C, Bartholomae CC, von Kalle C, Unterberg A, Herold- Mende C, Hofer S, Kulozik AE, von Deimling A, Scheurlen W, Felsberg J, Reifenberger G, Hasselblatt M, Crawford JR, Grant GA, Jabado N, Perry A, Cowdrey C, Croul S, Zadeh G, Korbel JO, Doz F, Delattre O, Bader GD, McCabe MG, Collins VP, Kieran MW, Cho YJ, Pomeroy SL, Witt O, Brors B, Taylor MD, Schüller U, Korshunov A, Eils R, Wechsler-Reya RJ, Lichter P, Pfister SM; ICGC PedBrain Tumor Project. Genome sequencing of SHH medulloblastoma predicts genotype- related response to smoothened inhibition. Cancer Cell. 2014 Mar 17;25(3):393-405. doi: 10.1016/j.ccr.2014.02.004. PMID: 24651015; PMCID: PMC4493053.

592: Racine E, Bell E, Yan A, Andrew G, Bell LE, Clarke M, Dubljevic V, Goldowitz D, Janvier A, McLachlan K, Muhajarine N, Nicholas D, Oskoui M, Rasmussen C, Rasmussen LA, Roberts W, Shevell M, Wade L, Yager JY. Ethics challenges of transition from paediatric to adult health care services for young adults with neurodevelopmental disabilities. Paediatr Child Health. 2014 Feb;19(2):65-8. doi: 10.1093/pch/19.2.65. PMID: 24596475; PMCID: PMC3941669.

593: Mack SC, Witt H, Piro RM, Gu L, Zuyderduyn S, Stütz AM, Wang X, Gallo M, Garzia L, Zayne K, Zhang X, Ramaswamy V, Jäger N, Jones DT, Sill M, Pugh TJ, Ryzhova M, Wani KM, Shih DJ, Head R, Remke M, Bailey SD, Zichner T, Faria CC, Barszczyk M, Stark S, Seker-Cin H, Hutter S, Johann P, Bender S, Hovestadt V, Tzaridis T, Dubuc AM, Northcott PA, Peacock J, Bertrand KC, Agnihotri S, Cavalli FM, Clarke I, Nethery-Brokx K, Creasy CL, Verma SK, Koster J, Wu X, Yao Y, Milde T, Sin-Chan P, Zuccaro J, Lau L, Pereira S, Castelo-Branco P, Hirst M, Marra MA, Roberts SS, Fults D, Massimi L, Cho YJ, Van Meter T, Grajkowska W, Lach B, Kulozik AE, von Deimling A, Witt O, Scherer SW, Fan X, Muraszko KM, Kool M, Pomeroy SL, Gupta N, Phillips J, Huang A, Tabori U, Hawkins C, Malkin D, Kongkham PN, Weiss WA, Jabado N, Rutka JT, Bouffet E, Korbel JO, Lupien M, Aldape KD, Bader GD, Eils R, Lichter P, Dirks PB, Pfister SM, Korshunov A, Taylor MD. Epigenomic alterations define lethal CIMP-positive ependymomas of infancy. Nature. 2014 Feb 27;506(7489):445-50. doi: 10.1038/nature13108. Epub 2014 Feb 19. PMID: 24553142; PMCID: PMC4174313.

594: van Karnebeek CD, Shevell M, Zschocke J, Moeschler JB, Stockler S. The metabolic evaluation of the child with an intellectual developmental disorder: diagnostic algorithm for identification of treatable causes and new digital resource. Mol Genet Metab. 2014 Apr;111(4):428-38. doi: 10.1016/j.ymgme.2014.01.011. Epub 2014 Jan 24. PMID: 24518794.

595: Smith ML, Olds J, Snyder T, Elliott I, Lach L, Whiting S. A follow-up study of cognitive function in young adults who had resective epilepsy surgery in childhood. Epilepsy Behav. 2014 Mar;32:79-83. doi: 10.1016/j.yebeh.2014.01.006. Epub 2014 Feb 7. PMID: 24508594.

596: Theeler BJ, Ellezam B, Sadighi ZS, Mehta V, Tran MD, Adesina AM, Bruner JM, Puduvalli VK. Adult pilocytic astrocytomas: clinical features and molecular analysis. Neuro Oncol. 2014 Jun;16(6):841-7. doi: 10.1093/neuonc/not246. Epub 2014 Jan 26. PMID: 24470550; PMCID: PMC4022218.

597: LeBlanc AC, Ramcharitar J, Afonso V, Hamel E, Bennett DA, Pakavathkumar P, Albrecht S. Caspase-6 activity in the CA1 region of the hippocampus induces age- dependent memory impairment. Cell Death Differ. 2014 May;21(5):696-706. doi: 10.1038/cdd.2013.194. Epub 2014 Jan 10. PMID: 24413155; PMCID: PMC3978300.

598: Owen M, Shevell M, Donofrio M, Majnemer A, McCarter R, Vezina G, Bouyssi- Kobar M, Evangelou I, Freeman D, Weisenfeld N, Limperopoulos C. Brain volume and neurobehavior in newborns with complex congenital heart defects. J Pediatr. 2014 May;164(5):1121-1127.e1. doi: 10.1016/j.jpeds.2013.11.033. Epub 2013 Dec 22. PMID: 24367983; PMCID: PMC4474232.

599: Kleinman CL, Gerges N, Papillon-Cavanagh S, Sin-Chan P, Pramatarova A, Quang DA, Adoue V, Busche S, Caron M, Djambazian H, Bemmo A, Fontebasso AM, Spence T, Schwartzentruber J, Albrecht S, Hauser P, Garami M, Klekner A, Bognar L, Montes JL, Staffa A, Montpetit A, Berube P, Zakrzewska M, Zakrzewski K, Liberski PP, Dong Z, Siegel PM, Duchaine T, Perotti C, Fleming A, Faury D, Remke M, Gallo M, Dirks P, Taylor MD, Sladek R, Pastinen T, Chan JA, Huang A, Majewski J, Jabado N. Fusion of TTYH1 with the C19MC microRNA cluster drives expression of a brain-specific DNMT3B isoform in the embryonal brain tumor ETMR. Nat Genet. 2014 Jan;46(1):39-44. doi: 10.1038/ng.2849. Epub 2013 Dec 8. PMID: 24316981.

600: Yu C, Ramgopal S, Libenson M, Abdelmoumen I, Powell C, Remy K, Madsen JR, Rotenberg A, Loddenkemper T. Outcomes of vagal nerve stimulation in a pediatric population: a single center experience. Seizure. 2014 Feb;23(2):105-11. doi: 10.1016/j.seizure.2013.10.002. Epub 2013 Oct 17. PMID: 24309238.

601: Aris IM, Soh SE, Tint MT, Liang S, Chinnadurai A, Saw SM, Rajadurai VS, Kwek K, Meaney MJ, Godfrey KM, Gluckman PD, Yap FK, Chong YS, Lee YS. Effect of maternal glycemia on neonatal adiposity in a multiethnic Asian birth cohort. J Clin Endocrinol Metab. 2014 Jan;99(1):240-7. doi: 10.1210/jc.2013-2738. Epub 2013 Dec 20. PMID: 24243635.

602: Bizik G, Picard M, Nijjar R, Tourjman V, McEwen BS, Lupien SJ, Juster RP. Allostatic load as a tool for monitoring physiological dysregulations and comorbidities in patients with severe mental illnesses. Harv Rev Psychiatry. 2013 Nov-Dec;21(6):296-313. doi: 10.1097/HRP.0000000000000012. PMID: 24201821.

603: Synofzik M, Bernard G, Lindig T, Gburek-Augustat J. Teaching neuroimages: hypomyelinating leukodystrophy with hypodontia due to POLR3B: look into a leukodystrophy's mouth. Neurology. 2013 Nov 5;81(19):e145. doi: 10.1212/01.wnl.0000435300.64776.7e. PMID: 24190003; PMCID: PMC3812106.

604: Verhey LH, Signori A, Arnold DL, Bar-Or A, Sadovnick AD, Marrie RA, Banwell B, Sormani MP. Clinical and MRI activity as determinants of sample size for pediatric multiple sclerosis trials. Neurology. 2013 Oct 1;81(14):1215-21. doi: 10.1212/WNL.0b013e3182a6cb9b. Epub 2013 Aug 21. PMID: 23966255; PMCID: PMC3795606.

605: Poliachik SL, Poliakov AV, Jansen LA, McDaniel SS, Wray CD, Kuratani J, Saneto RP, Ojemann JG, Novotny EJ Jr. Tissue localization during resective epilepsy surgery. Neurosurg Focus. 2013 Jun;34(6):E8. doi: 10.3171/2013.3.FOCUS1360. PMID: 23724842.

606: Dudley RW, Parolin M, Gagnon B, Saluja R, Yap R, Montpetit K, Ruck J, Poulin C, Cantin MA, Benaroch TE, Farmer JP. Long-term functional benefits of selective dorsal rhizotomy for spastic cerebral palsy. J Neurosurg Pediatr. 2013 Aug;12(2):142-50. doi: 10.3171/2013.4.PEDS12539. Epub 2013 May 28. PMID: 23713680.

607: Baird R, Guilbault MP, Tessier R, Ansermino JM. A systematic review and meta-analysis of caudal blockade versus alternative analgesic strategies for pediatric inguinal hernia repair. J Pediatr Surg. 2013 May;48(5):1077-85. doi: 10.1016/j.jpedsurg.2013.02.030. PMID: 23701786.

608: Garfinkle J, Sant'Anna GM, Wintermark P, Ali N, Morneault L, Koclas L, Shevell MI. Cooling in the real world: therapeutic hypothermia in hypoxic- ischemic encephalopathy. Eur J Paediatr Neurol. 2013 Sep;17(5):492-7. doi: 10.1016/j.ejpn.2013.03.006. Epub 2013 Apr 18. PMID: 23603010.

609: Zou Y, Chiu H, Zinovyeva A, Ambros V, Chuang CF, Chang C. Developmental decline in neuronal regeneration by the progressive change of two intrinsic timers. Science. 2013 Apr 19;340(6130):372-376. doi: 10.1126/science.1231321. PMID: 23599497; PMCID: PMC4074024.

610: Dufresne D, Hamdan FF, Rosenfeld JA, Torchia B, Rosenblatt B, Michaud JL, Srour M. Homozygous deletion of Tenascin-R in a patient with intellectual disability. J Med Genet. 2012 Jul;49(7):451-4. doi: 10.1136/jmedgenet-2012-100831. Epub 2012 Jun 22. PMID: 22730557; PMCID: PMC3395313.

611: Bretholz A, Doan Q, Cheng A, Lauder G. A presurvey and postsurvey of a web- and simulation-based course of ultrasound-guided nerve blocks for pediatric emergency medicine. Pediatr Emerg Care. 2012 Jun;28(6):506-9. doi: 10.1097/PEC.0b013e3182586f42. PMID: 22653464.

612: Shevell M. A Canadian paradox: Tommy Douglas and eugenics. Can J Neurol Sci. 2012 Jan;39(1):35-9. doi: 10.1017/s0317167100012658. PMID: 22384493.

613: Martin K, Baird R, Farmer JP, Emil S, Laberge JM, Shaw K, Puligandla P. The use of laparoscopy in ventriculoperitoneal shunt revisions. J Pediatr Surg. 2011 Nov;46(11):2146-50. doi: 10.1016/j.jpedsurg.2011.07.001. PMID: 22075347.

614: Shevell MI. A brief synopsis of the “why, what, and how” of teaching ethics to pediatric neurology trainees. Semin Pediatr Neurol. 2011 Jun;18(2):79-80. doi: 10.1016/j.spen.2011.05.009. PMID: 22036484.

615: Garfinkle J, Andermann F, Shevell MI. Neurolathyrism in vapniarka: medical heroism in a concentration Camp. Can J Neurol Sci. 2011 Nov;38(6):839-44. doi: 10.1017/s0317167100012403. PMID: 22030420.

616: Bernard G, Chouery E, Putorti ML, Tétreault M, Takanohashi A, Carosso G, Clément I, Boespflug-Tanguy O, Rodriguez D, Delague V, Abou Ghoch J, Jalkh N, Dorboz I, Fribourg S, Teichmann M, Megarbane A, Schiffmann R, Vanderver A, Brais B. Mutations of POLR3A encoding a catalytic subunit of RNA polymerase Pol III cause a recessive hypomyelinating leukodystrophy. Am J Hum Genet. 2011 Sep 9;89(3):415-23. doi: 10.1016/j.ajhg.2011.07.014. Erratum in: Am J Hum Genet. 2012 Nov 2;91(5):972. PMID: 21855841; PMCID: PMC3169829.

617: Hasan A, Palumbo M, Atkinson J, Carret AS, Farmer JP, Montes J, Albrecht S, Saint-Martin C, Freeman CR. Treatment-related morbidity in atypical teratoid/rhabdoid tumor: multifocal necrotizing leukoencephalopathy. Pediatr Neurosurg. 2011;47(1):7-14. doi: 10.1159/000323412. Epub 2011 May 26. PMID: 21613772.

618: Garfinkle J, Shevell MI. Predictors of outcome in term infants with neonatal seizures subsequent to intrapartum asphyxia. J Child Neurol. 2011 Apr;26(4):453-9. doi: 10.1177/0883073810382907. Epub 2011 Jan 26. PMID: 21270469.

619: Garon ML, Rufiange M, Hamilton R, McCulloch DL, Lachapelle P. Asymmetrical growth of the photopic hill during the light adaptation effect. Doc Ophthalmol. 2010 Dec;121(3):177-87. doi: 10.1007/s10633-010-9243-0. Epub 2010 Aug 15. PMID: 20711798.

620: Limperopoulos C. Extreme prematurity, cerebellar injury, and autism. Semin Pediatr Neurol. 2010 Mar;17(1):25-9. doi: 10.1016/j.spen.2010.01.003. PMID: 20434689.

621: Self L, Shevell MI; REPACQ Consortium. A registry-based assessment of cerebral palsy and cerebral malformations. J Child Neurol. 2010 Nov;25(11):1313-8. doi: 10.1177/0883073810362759. Epub 2010 Mar 11. PMID: 20223748.

622: Shevell MI. The terms diplegia and quadriplegia should not be abandoned. Dev Med Child Neurol. 2010 Jun;52(6):508-9. doi: 10.1111/j.1469-8749.2009.03566.x. Epub 2009 Dec 18. PMID: 20030685.

623: Al-Macki N, Miller SP, Hall N, Shevell M. The spectrum of abnormal neurologic outcomes subsequent to term intrapartum asphyxia. Pediatr Neurol. 2009 Dec;41(6):399-405. doi: 10.1016/j.pediatrneurol.2009.06.001. PMID: 19931160.

624: Shamji MF, Vassilyadi M, Lam CH, Montes JL, Farmer JP. Congenital tumors of the central nervous system: the MCH experience. Pediatr Neurosurg. 2009;45(5):368-74. doi: 10.1159/000257526. Epub 2009 Nov 11. PMID: 19907201.

625: Frigon C, Loetwiriyakul W, Ranger M, Otis A. An acute pain service improves postoperative pain management for children undergoing selective dorsal rhizotomy. Paediatr Anaesth. 2009 Dec;19(12):1213-9. doi: 10.1111/j.1460-9592.2009.03184.x. Epub 2009 Oct 23. PMID: 19863740.

626: Shevell MI. Current understandings and challenges in the management of cerebral palsy. Minerva Pediatr. 2009 Aug;61(4):399-413. PMID: 19752849.

627: Shevell MI. Present conceptualization of early childhood neurodevelopmental disabilities. J Child Neurol. 2010 Jan;25(1):120-6. doi: 10.1177/0883073809336122. Epub 2009 Sep 8. PMID: 19738235.

628: Sloan ME, Simard-Tremblay E, Shevell MI. Features of a subset of children with complex partial epilepsy requiring combination therapy for effective seizure control. J Child Neurol. 2010 Jan;25(1):43-7. doi: 10.1177/0883073809336126. Epub 2009 Jun 3. PMID: 19494358.

629: Ryckman J, Laberge JM, Puligandla PS. Paraplegia after chest wall resection for primitive neuroectodermal tumor. Semin Pediatr Surg. 2009 May;18(2):113-5. doi: 10.1053/j.sempedsurg.2009.02.010. PMID: 19349002.

630: Shevell M. The tripartite origins of the tonic neck reflex: Gesell, Gerstmann, and Magnus. Neurology. 2009 Mar 3;72(9):850-3. doi: 10.1212/01.wnl.0000343961.35429.09. PMID: 19255413.

631: Bernard G, Shevell M. The wobbly child: an approach to inherited ataxias. Semin Pediatr Neurol. 2008 Dec;15(4):194-208. doi: 10.1016/j.spen.2008.10.011. PMID: 19073328.

632: Venkateswaran S, Shevell M. The case against routine electroencephalography in specific language impairment. Pediatrics. 2008 Oct;122(4):e911-6. doi: 10.1542/peds.2008-0257. Epub 2008 Sep 15. PMID: 18794194.

633: Frigon C, Sedeek K, Poulin C, Brown K, Farmer JP. Does ketamine affect intraoperative electrophysiological monitoring in children undergoing selective posterior rhizotomy? Paediatr Anaesth. 2008 Sep;18(9):831-7. doi: 10.1111/j.1460-9592.2008.02687.x. PMID: 18768043.

634: Crevier L, Mercier C. L'organisation de la transition enfant à adulte en neurochirurgie pédiatrique au Canada [The organization of the transition from childhood to adulthood in pediatric neurosurgery in Canada]. Neurochirurgie. 2008 Oct;54(5):583-6. French. doi: 10.1016/j.neuchi.2008.07.006. Epub 2008 Aug 26. PMID: 18752813.

635: Nadler B, Shevell MI. Childhood absence epilepsy requiring more than one medication for seizure control. Can J Neurol Sci. 2008 Jul;35(3):297-300. PMID: 18714796.

636: Webster RI, Erdos C, Evans K, Majnemer A, Saigal G, Kehayia E, Thordardottir E, Evans A, Shevell MI. Neurological and magnetic resonance imaging findings in children with developmental language impairment. J Child Neurol. 2008 Aug;23(8):870-7. doi: 10.1177/0883073808315620. PMID: 18660471.

637: Ang C, Hauerstock D, Guiot MC, Kasymjanova G, Roberge D, Kavan P, Muanza T. Characteristics and outcomes of medulloblastoma in adults. Pediatr Blood Cancer. 2008 Nov;51(5):603-7. doi: 10.1002/pbc.21588. PMID: 18649371.

638: Bernard G, Riou E, Rosenblatt B, Dilenge ME, Poulin C. Simultaneous Guillain-Barré syndrome and acute disseminated encephalomyelitis in the pediatric population. J Child Neurol. 2008 Jul;23(7):752-7. doi: 10.1177/0883073808314360. Epub 2008 Mar 19. PMID: 18354151.

639: Bernard G, Shevell MI. Channelopathies: a review. Pediatr Neurol. 2008 Feb;38(2):73-85. doi: 10.1016/j.pediatrneurol.2007.09.007. PMID: 18206787.

640: Racine J, Behn D, Lachapelle P. Structural and functional maturation of the retina of the albino Hartley guinea pig. Doc Ophthalmol. 2008 Jul;117(1):13-26. doi: 10.1007/s10633-007-9098-1. Epub 2007 Nov 22. PMID: 18034273.

641: Farmer JP, Sabbagh AJ. Selective dorsal rhizotomies in the treatment of spasticity related to cerebral palsy. Childs Nerv Syst. 2007 Sep;23(9):991-1002. doi: 10.1007/s00381-007-0398-2. Epub 2007 Jul 21. PMID: 17643249.

642: Shevell M. Office evaluation of the child with developmental delay. Semin Pediatr Neurol. 2006 Dec;13(4):256-61. doi: 10.1016/j.spen.2006.09.006. PMID: 17178355.

643: Frigon C, Mai R, Valois-Gomez T, Desparmet J. Bowel hematoma following an iliohypogastric-ilioinguinal nerve block. Paediatr Anaesth. 2006 Sep;16(9):993-6. doi: 10.1111/j.1460-9592.2006.01909.x. PMID: 16918666.

644: Srour M, Mazer B, Shevell MI. Analysis of clinical features predicting etiologic yield in the assessment of global developmental delay. Pediatrics. 2006 Jul;118(1):139-45. doi: 10.1542/peds.2005-2702. PMID: 16818559.

645: Majnemer A, Limperopoulos C, Shevell M, Rohlicek C, Rosenblatt B, Tchervenkov C. Health and well-being of children with congenital cardiac malformations, and their families, following open-heart surgery. Cardiol Young. 2006 Apr;16(2):157-64. doi: 10.1017/S1047951106000096. PMID: 16553978.

646: Oskoui M, Webster RI, Zhang X, Shevell MI. Factors predictive of outcome in childhood epilepsy. J Child Neurol. 2005 Nov;20(11):898-904. doi: 10.1177/08830738050200110701. PMID: 16417860.

647: Mittal S, Montes JL, Farmer JP, Rosenblatt B, Dubeau F, Andermann F, Poulin N, Olivier A. Long-term outcome after surgical treatment of temporal lobe epilepsy in children. J Neurosurg. 2005 Nov;103(5 Suppl):401-12. doi: 10.3171/ped.2005.103.5.0401. PMID: 16302611.

648: Shevell M, Majnemer A, Platt RW, Webster R, Birnbaum R. Developmental and functional outcomes in children with global developmental delay or developmental language impairment. Dev Med Child Neurol. 2005 Oct;47(10):678-83. doi: 10.1017/S0012162205001386. PMID: 16174311.

649: Oskoui M, Shevell MI. Profile of pediatric hemiparesis. J Child Neurol. 2005 Jun;20(6):471-6. doi: 10.1177/088307380502000601. PMID: 15996394.

650: Shevell MI, Majnemer A, Webster RI, Platt RW, Birnbaum R. Outcomes at school age of preschool children with developmental language impairment. Pediatr Neurol. 2005 Apr;32(4):264-9. doi: 10.1016/j.pediatrneurol.2004.12.008. PMID: 15797183.

651: Shevell MI. The “Bermuda triangle” of neonatal neurology: cerebral palsy, neonatal encephalopathy, and intrapartum asphyxia. Semin Pediatr Neurol. 2004 Mar;11(1):24-30. doi: 10.1016/j.spen.2004.01.005. PMID: 15132251.

652: Shevell MI. The ethics of case reports. Paediatr Child Health. 2004 Feb;9(2):83-4. doi: 10.1093/pch/9.2.83. PMID: 19654984; PMCID: PMC2720465.

653: Racine J, Behn D, Simard E, Lachapelle P. Spontaneous occurrence of a potentially night blinding disorder in guinea pigs. Doc Ophthalmol. 2003 Jul;107(1):59-69. doi: 10.1023/a:1024435911882. PMID: 12906123.

654: Behn D, Doke A, Racine J, Casanova C, Chemtob S, Lachapelle P. Dark adaptation is faster in pigmented than albino rats. Doc Ophthalmol. 2003 Mar;106(2):153-9. doi: 10.1023/a:1022511918823. PMID: 12678280.

655: Al-Twajri WA, Shevell MI. Atypical benign epilepsy of childhood with rolandic spikes: features of a subset requiring more than one medication for seizure control. J Child Neurol. 2002 Dec;17(12):901-4. PMID: 12593463.

656: Shevell MI. Clinical and diagnostic profile of agenesis of the corpus callosum. J Child Neurol. 2002 Dec;17(12):896-900. PMID: 12593462.

657: Shevell M. Hallervorden and history. N Engl J Med. 2003 Jan 2;348(1):3-4. doi: 10.1056/NEJMp020158. PMID: 12510036.

658: Mittal S, Farmer JP, Al-Atassi B, Montpetit K, Gervais N, Poulin C, Benaroch TE, Cantin MA. Functional performance following selective posterior rhizotomy: long-term results determined using a validated evaluative measure. J Neurosurg. 2002 Sep;97(3):510-8. doi: 10.3171/jns.2002.97.3.0510. PMID: 12296632.

659: Farmer JP, Khan S, Khan A, Ortenberg J, Freeman C, O'Gorman AM, Montes J. Neurofibromatosis type 1 and the pediatric neurosurgeon: a 20-year institutional review. Pediatr Neurosurg. 2002 Sep;37(3):122-36. doi: 10.1159/000064398. PMID: 12187057.

660: Mittal S, Farmer JP, Al-Atassi B, Gibis J, Kennedy E, Galli C, Courchesnes G, Poulin C, Cantin MA, Benaroch TE. Long-term functional outcome after selective posterior rhizotomy. J Neurosurg. 2002 Aug;97(2):315-25. doi: 10.3171/jns.2002.97.2.0315. PMID: 12186459.

661: Al-Twaijri WA, Shevell MI. A novel chronic childhood sensory predominant neuropathy. Pediatr Neurol. 2002 Jul;27(1):49-52. doi: 10.1016/s0887-8994(02)00376-4. PMID: 12160974.

662: Limperopoulos C, Majnemer A, Shevell MI, Rohlicek C, Rosenblatt B, Tchervenkov C, Darwish HZ. Predictors of developmental disabilities after open heart surgery in young children with congenital heart defects. J Pediatr. 2002 Jul;141(1):51-8. doi: 10.1067/mpd.2002.125227. PMID: 12091851.

663: Dembinska O, Rojas LM, Chemtob S, Lachapelle P. Evidence for a brief period of enhanced oxygen susceptibility in the rat model of oxygen-induced retinopathy. Invest Ophthalmol Vis Sci. 2002 Jul;43(7):2481-90. PMID: 12091454.

664: Al-Twaijri WA, Shevell MI. Pediatric migraine equivalents: occurrence and clinical features in practice. Pediatr Neurol. 2002 May;26(5):365-8. doi: 10.1016/s0887-8994(01)00416-7. PMID: 12057796.

665: Mittal S, Farmer JP, Al-Atassi B, Montpetit K, Gervais N, Poulin C, Cantin MA, Benaroch TE. Impact of selective posterior rhizotomy on fine motor skills. Long-term results using a validated evaluative measure. Pediatr Neurosurg. 2002 Mar;36(3):133-41. doi: 10.1159/000048368. PMID: 11919447.

666: Nguyen TN, Polomeno RC, Farmer JP, Montes JL. Ophthalmic complications of slit-ventricle syndrome in children. Ophthalmology. 2002 Mar;109(3):520-4; discussion 524-5. doi: 10.1016/s0161-6420(01)00985-x. PMID: 11874754.

667: Majnemer A, Desrosiers J, Gauthier J, Dutil E, Robichaud L, Rousseau J, Hébert L. Involvement of occupational therapy departments in research: a provincial survey. Can J Occup Ther. 2001 Dec;68(5):272-9. doi: 10.1177/000841740106800503. PMID: 11765666.

668: Mittal S, Farmer JP, Poulin C, Silver K. Reliability of intraoperative electrophysiological monitoring in selective posterior rhizotomy. J Neurosurg. 2001 Jul;95(1):67-75. doi: 10.3171/jns.2001.95.1.0067. PMID: 11453400.

669: Shevell MI, Majnemer A, Rosenbaum P, Abrahamowicz M. Etiologic determination of childhood developmental delay. Brain Dev. 2001 Jul;23(4):228-35. doi: 10.1016/s0387-7604(01)00212-1. PMID: 11377001.

670: Farmer JP, Montes JL, Freeman CR, Meagher-Villemure K, Bond MC, O'Gorman AM. Brainstem Gliomas. A 10-year institutional review. Pediatr Neurosurg. 2001 Apr;34(4):206-14. doi: 10.1159/000056021. PMID: 11359114.

671: Mittal S, Farmer JP, Rosenblatt B, Andermann F, Montes JL, Villemure JG. Intractable epilepsy after a functional hemispherectomy: important lessons from an unusual case. Case report. J Neurosurg. 2001 Mar;94(3):510-4. doi: 10.3171/jns.2001.94.3.0510. PMID: 11235958.

672: Rousseau S, Lachapelle P. The electroretinogram recorded at the onset of dark-adaptation: understanding the origin of the scotopic oscillatory potentials. Doc Ophthalmol. 1999;99(2):135-50. doi: 10.1023/a:1002679932462. PMID: 11097118.

673: Limperopoulos C, Majnemer A, Shevell MI, Rosenblatt B, Rohlicek C, Tchervenkov C. Neurodevelopmental status of newborns and infants with congenital heart defects before and after open heart surgery. J Pediatr. 2000 Nov;137(5):638-45. doi: 10.1067/mpd.2000.109152. PMID: 11060529.

674: Shevell M. Confronting the past: Contemporary German paediatric response to medical practice in the Third Reich. Paediatr Child Health. 2000 Nov;5(8):451-2. doi: 10.1093/pch/5.8.451. PMID: 20177554; PMCID: PMC2819958.

675: Miller SP, Shevell MI, Patenaude Y, O'Gorman AM. Neuromotor spectrum of periventricular leukomalacia in children born at term. Pediatr Neurol. 2000 Aug;23(2):155-9. doi: 10.1016/s0887-8994(00)00172-7. PMID: 11020641.

676: Modha A, Vassilyadi M, George A, Kuehn S, Hsu E, Ventureyra EC. Medulloblastoma in children–the Ottawa experience. Childs Nerv Syst. 2000 Jun;16(6):341-50. doi: 10.1007/s003810050529. PMID: 10933229.

677: Miller SP, O'Gorman AM, Shevell MI. Recurrent artery of Heubner infarction in infancy. Dev Med Child Neurol. 2000 May;42(5):344-6. doi: 10.1017/s0012162200000608. PMID: 10855656.

678: Vernet O, Montes JL, Farmer JP, Blundell JE, Bertrand G, Freeman CR. Long term results of multimodality treatment of craniopharyngioma in children. J Clin Neurosci. 1999 May;6(3):199-203. doi: 10.1054/jocn.1998.0041. PMID: 10835167.

679: Painson JC, Veldhuis JD, Tannenbaum GS. Single exposure to testosterone in adulthood rapidly induces regularity in the growth hormone release process. Am J Physiol Endocrinol Metab. 2000 May;278(5):E933-40. doi: 10.1152/ajpendo.2000.278.5.E933. PMID: 10780951.

680: Rousseau S, Lachapelle P. Transient enhancing of cone electroretinograms following exposure to brighter photopic backgrounds. Vision Res. 2000;40(8):1013-8. doi: 10.1016/s0042-6989(99)00245-x. PMID: 10720670.

681: Rilliet B, de Paul Djientcheu V, Vernet O, Montes J, Farmer JP, Bertrand G. Craniopharyngiomas, results in children and adolescents operated through a transsphenoidal approach compared with an intracranial approach. Front Radiat Ther Oncol. 1999;33:114-22. doi: 10.1159/000061228. PMID: 10549482.

682: Majnemer A, Limperopoulos C. Developmental progress of children with congenital heart defects requiring open heart surgery. Semin Pediatr Neurol. 1999 Mar;6(1):12-9. doi: 10.1016/s1071-9091(99)80042-4. PMID: 10098225.

683: Majnemer A, Mazer B. Neurologic evaluation of the newborn infant: definition and psychometric properties. Dev Med Child Neurol. 1998 Oct;40(10):708-15. doi: 10.1111/j.1469-8749.1998.tb12332.x. PMID: 9851241.

684: Wagner C, Caplan SR, Tannenbaum GS. Genesis of the ultradian rhythm of GH secretion: a new model unifying experimental observations in rats. Am J Physiol. 1998 Dec;275(6):E1046-54. doi: 10.1152/ajpendo.1998.275.6.E1046. PMID: 9843748.

685: Houle AM, Vernet O, Jednak R, Pippi Salle JL, Farmer JP. Bladder function before and after selective dorsal rhizotomy in children with cerebral palsy. J Urol. 1998 Sep;160(3 Pt 2):1088-91. doi: 10.1097/00005392-199809020-00032. PMID: 9719282.

686: Shevell MI. Clinical ethics and developmental delay. Semin Pediatr Neurol. 1998 Mar;5(1):70-5. doi: 10.1016/s1071-9091(98)80021-1. PMID: 9548644.

687: Shevell MI. The evaluation of the child with a global developmental delay. Semin Pediatr Neurol. 1998 Mar;5(1):21-6. doi: 10.1016/s1071-9091(98)80014-4. PMID: 9548637.

688: Shevell MI. Neurology's witness to history: part II. Leo Alexander's contributions to the Nuremberg Code (1946 to 1947). Neurology. 1998 Jan;50(1):274-8. doi: 10.1212/wnl.50.1.274. PMID: 9443492.

689: Roy S, Martel J, Tenenhouse HS. Growth hormone normalizes renal 1,25-dihydroxyvitamin D3-24-hydroxylase gene expression but not Na+-phosphate cotransporter (Npt2) mRNA in phosphate-deprived Hyp mice. J Bone Miner Res. 1997 Oct;12(10):1672-80. doi: 10.1359/jbmr.1997.12.10.1672. PMID: 9333128.

690: Ludemann JP, Tewfik TL, Meagher-Villemure K, Bernard C. Congenital mesenchymoma transgressing the cribriform plate. J Otolaryngol. 1997 Aug;26(4):270-2. PMID: 9263898.

691: Lam CH, Montes J, Farmer JP, O'Gorman AM, Meagher-Villemure K. Traumatic aneurysm from shaken baby syndrome: case report. Neurosurgery. 1996 Dec;39(6):1252-5. doi: 10.1097/00006123-199612000-00041. PMID: 8938784.

692: Feindel W. Neurosurgery at the Montreal Neurological Institute and McGill University Hospitals. Neurosurgery. 1996 Oct;39(4):830-9. doi: 10.1097/00006123-199610000-00038. PMID: 8880779.

693: Vernet O, Farmer JP, Houle AM, Montes JL. Impact of urodynamic studies on the surgical management of spinal cord tethering. J Neurosurg. 1996 Oct;85(4):555-9. doi: 10.3171/jns.1996.85.4.0555. PMID: 8814155.

694: Lacroix M, Farmer JP, Meagher-Villemure K, Rosenblatt B, Montes JL. Cauda equina histiocytosis X. Pediatr Neurol. 1996 Apr;14(3):231-5. doi: 10.1016/0887-8994(96)00081-1. PMID: 8736408.

695: Vernet O, Montes JL, O'Gorman AM, Baruchel S, Farmer JP. Encephaloduroarterio-synangiosis in a child with sickle cell anemia and moyamoya disease. Pediatr Neurol. 1996 Apr;14(3):226-30. doi: 10.1016/0887-8994(96)00045-8. PMID: 8736407.

696: Robb P. Personal reminiscences: the development of neurology at the Montreal Children's Hospital. Pediatr Neurol. 1996 Apr;14(3):185-8. doi: 10.1016/0887-8994(96)00061-6. PMID: 8736400.

697: Vernet O, Farmer JP, Montes JL. Comparison of syringopleural and syringosubarachnoid shunting in the treatment of syringomyelia in children. J Neurosurg. 1996 Apr;84(4):624-8. doi: 10.3171/jns.1996.84.4.0624. PMID: 8613854.

698: Vernet O, Farmer JP, Lambert R, Montes JL. Radionuclide shuntogram: adjunct to manage hydrocephalic patients. J Nucl Med. 1996 Mar;37(3):406-10. PMID: 8772632.

699: Côté A, Porras H, Meehan B. Age-dependent vulnerability to carotid chemodenervation in piglets. J Appl Physiol (1985). 1996 Jan;80(1):323-31. doi: 10.1152/jappl.1996.80.1.323. PMID: 8847323.

700: Vernet O, Farmer JP, Meagher-Villemure K, Montes JL. Supratentorial ectopic ependymoma. Can J Neurol Sci. 1995 Nov;22(4):316-9. doi: 10.1017/s0317167100039561. PMID: 8599779.

701: Vassilyadi M, Farmer JP, Montes JL. Negative-pressure hydrocephalus. J Neurosurg. 1995 Sep;83(3):486-90. doi: 10.3171/jns.1995.83.3.0486. PMID: 7666227.

702: Majnemer A, Shevell MI. Diagnostic yield of the neurologic assessment of the developmentally delayed child. J Pediatr. 1995 Aug;127(2):193-9. doi: 10.1016/s0022-3476(95)70294-6. PMID: 7543566.

703: Lam CH, Farmer JP, Meagher-Villemure K, Montes JL. Masson's vegetant haemangio-endothelioma. Pediatr Neurosurg. 1995;23(2):93-6. doi: 10.1159/000120943. PMID: 8555102.

704: Montes JL, Rosenblatt B, Farmer JP, O'Gorman AM, Andermann F, Watters GV, Meagher-Villemure K. Lesionectomy of MRI detected lesions in children with epilepsy. Pediatr Neurosurg. 1995;22(4):167-73. doi: 10.1159/000120897. PMID: 7619716.

705: Ross IB, Shevell MI, Montes JL, Rosenblatt B, Watters GV, Farmer JP, O'Gorman AM. Encephaloduroarteriosynangiosis (EDAS) for the treatment of childhood moyamoya disease. Pediatr Neurol. 1994 May;10(3):199-204. doi: 10.1016/0887-8994(94)90023-x. PMID: 8060421.

706: Montes JL, Clarke DB, Farmer JP. Stereotactic transtentorial hiatus ventriculoperitoneal shunting for the sequestered fourth ventricle. Technical note. J Neurosurg. 1994 Apr;80(4):759-61. doi: 10.3171/jns.1994.80.4.0759. PMID: 8151361.

707: Clarke DB, Farmer JP, Montes JL, Watters GV, Rouleau G. Newborn apnea caused by a neurofibroma at the craniocervical junction. Can J Neurol Sci. 1994 Feb;21(1):64-6. doi: 10.1017/s0317167100048800. PMID: 8180909.

708: Baltuch GH, Farmer JP, Meagher-Villemure K, O'Gorman AM, Montes JL. Ganglioglioma presenting as a vascular lesion in a 10-year-old boy. Case report. J Neurosurg. 1993 Dec;79(6):920-3. doi: 10.3171/jns.1993.79.6.0920. PMID: 8246060.

709: Shevell MI, Silver K, Watters GV, Rosenblatt B. Transient oculosympathetic paresis (group II Raeder paratrigeminal neuralgia) of childhood: migraine variant. Pediatr Neurol. 1993 Jul-Aug;9(4):289-92. doi: 10.1016/0887-8994(93)90065-k. PMID: 8216541.

710: Giroux M, Farmer JP, Meagher-Villemure KM, O'Gorman AM, Montes JL. Intraventricular central neurocytoma. Can J Neurol Sci. 1992 Aug;19(3):392-6. PMID: 1393851.

711: Trasler JM, Alcivar AA, Awoniyi CA, Santulli R, Zirkin BR, Hecht NB. Temporal gene expression is restored concomitantly with germ cells in the experimentally regressed rat testis. Endocrinology. 1992 Jul;131(1):297-304. doi: 10.1210/endo.131.1.1612009. PMID: 1612009.

712: Munz M, Farmer JP, Auger L, O'Gorman AM, Schloss MD. Otitis media and CNS complications. J Otolaryngol. 1992 Jun;21(3):224-6. PMID: 1404577.

713: Wiesel S, Bevan JC, Samuel J, Donati F. Vecuronium neuromuscular blockade in a child with mitochondrial myopathy. Anesth Analg. 1991 May;72(5):696-9. doi: 10.1213/00000539-199105000-00020. PMID: 1673325.

714: Benoit J, Lachapelle P. Temporal relationship between ERG components and geniculate unit activity in rabbit. Vision Res. 1990;30(6):797-806. doi: 10.1016/0042-6989(90)90048-p. PMID: 2385920.

715: Gardner DJ, O'Gorman AM, Blundell JE. Intraspinal epidermoid tumour: late complication of lumbar puncture. CMAJ. 1989 Aug 1;141(3):223-5. PMID: 2752348; PMCID: PMC1269411.

716: Tenenhouse HS, Klugerman AH, Gurd W, Lapointe M, Tannenbaum GS. Pituitary involvement in renal adaptation to phosphate deprivation. Am J Physiol. 1988 Sep;255(3 Pt 2):R373-8. doi: 10.1152/ajprenal.1988.255.3.F373. PMID: 3414832.