Department of Neurosurgery, Istanbul Bilim University, Istanbul, Turkey.
1: Canaz H, Alatas I, Saracoglu A, Ozel K, Gedikbasi A. Open Fetal Surgery in Turkey. Fetal Diagn Ther. 2018 Oct 9:1-2. doi: 10.1159/000492818. [Epub ahead of print] PubMed PMID: 30300900.
2: Aydın S, Canaz H, Topcular B, Benackova Z. Major Depression and Obsessive-compulsive Disorder Treated with Deep Brain Stimulation of Bilateral Nucleus Accumbens: The First Case of Turkey. Asian J Neurosurg. 2018 Jul-Sep;13(3):842-844. doi: 10.4103/ajns.AJNS_319_16. PubMed PMID: 30283561; PubMed Central PMCID: PMC6159045.
3: Kitis S, Coskun ZM, Tasdemir P, Tuncez E, Zamani AG, Acar A. Analysis of genetic polymorphisms associated with intervertebral disc degeneration. Cell Mol Biol (Noisy-le-grand). 2018 Jul 30;64(10):61-65. PubMed PMID: 30084796.
4: Schaffer AE, Breuss MW, Caglayan AO, Al-Sanaa N, Al-Abdulwahed HY, Kaymakçalan H, Yılmaz C, Zaki MS, Rosti RO, Copeland B, Baek ST, Musaev D, Scott EC, Ben-Omran T, Kariminejad A, Kayserili H, Mojahedi F, Kara M, Cai N, Silhavy JL, Elsharif S, Fenercioglu E, Barshop BA, Kara B, Wang R, Stanley V, James KN, Nachnani R, Kalur A, Megahed H, Incecik F, Danda S, Alanay Y, Faqeih E, Melikishvili G, Mansour L, Miller I, Sukhudyan B, Chelly J, Dobyns WB, Bilguvar K, Jamra RA, Gunel M, Gleeson JG. Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration. Nat Genet. 2018 Aug;50(8):1093-1101. doi: 10.1038/s41588-018-0166-0. Epub 2018 Jul 16. PubMed PMID: 30013181; PubMed Central PMCID: PMC6072555.
5: Alatas I, Canaz G, Arslan G, Cevik S, Kacmaz B, Kara N, Canaz H. Analysis of Denver Neurodevelopmental Screening Test Results of Myelomeningocele, Hydrocephalus, and Microcephaly Patients. J Pediatr Neurosci. 2018 Jan-Mar;13(1):28-33. doi: 10.4103/JPN.JPN_156_17. PubMed PMID: 29899768; PubMed Central PMCID: PMC5982489.
6: Canaz H, Karalok I, Topcular B, Agaoglu M, Yapici Z, Aydin S. DBS in pediatric patients: institutional experience. Childs Nerv Syst. 2018 Sep;34(9):1771-1776. doi: 10.1007/s00381-018-3839-1. Epub 2018 May 24. PubMed PMID: 29797064.
7: Çevik S, Katar S, Hanımoǧlu H. C1-C2 Transverse Foramen Decompression by Anterolateral Approach as an Alternative Treatment in Bow Hunter's Syndrome. Asian J Neurosurg. 2018 Apr-Jun;13(2):411-413. doi: 10.4103/ajns.AJNS_338_16. PubMed PMID: 29682046; PubMed Central PMCID: PMC5898117.
8: Kasap M, Canaz H, Canaz G, Tokmak M, Bingul A, Alatas I. Morphometric Analysis of Dose-dependent Effect of Progesterone on Experimental Vasospasm-induced Rat Femoral Arteries. Asian J Neurosurg. 2018 Apr-Jun;13(2):271-276. doi: 10.4103/1793-5482.228567. PubMed PMID: 29682020; PubMed Central PMCID: PMC5898091.
9: Kocoglu C, Gundogdu A, Kocaman G, Kahraman-Koytak P, Uluc K, Kiziltan G, Caglayan AO, Bilguvar K, Vural A, Basak AN. Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families. Neurol Genet. 2018 Jan 18;4(1):e218. doi: 10.1212/NXG.0000000000000218. eCollection 2018 Feb. PubMed PMID: 29379883; PubMed Central PMCID: PMC5773845.
10: Canaz H, Alatas I, Canaz G, Gumussuyu G, Cacan MA, Saracoglu A, Ucar BY. Surgical treatment of patients with myelomeningocele-related spine deformities: study of 26 cases. Childs Nerv Syst. 2018 Jul;34(7):1367-1374. doi: 10.1007/s00381-018-3731-z. Epub 2018 Jan 25. PubMed PMID: 29372371.
11: Kaymakcalan H, Yarman Y, Goc N, Toy F, Meral C, Ercan-Sencicek AG, Gunel M. Novel compound heterozygous mutations in GPT2 linked to microcephaly, and intellectual developmental disability with or without spastic paraplegia. Am J Med Genet A. 2018 Feb;176(2):421-425. doi: 10.1002/ajmg.a.38558. Epub 2017 Dec 11. PubMed PMID: 29226631.
12: Alatas I, Canaz G, Kayran NA, Kara N, Canaz H. Shunt revision rates in myelomeningocele patients in the first year of life: a retrospective study of 52 patients. Childs Nerv Syst. 2018 May;34(5):919-923. doi: 10.1007/s00381-017-3663-z. Epub 2017 Nov 20. PubMed PMID: 29159427.
13: Canaz H, Canaz G, Dogan I, Alatas I. Health-related quality of life in non-paraplegic (ambulatory) children with myelomeningocele. Childs Nerv Syst. 2017 Nov;33(11):1997-2002. doi: 10.1007/s00381-017-3494-y. Epub 2017 Jun 27. PubMed PMID: 28656385.
14: Çağlayan AO, Sezer RG, Kaymakçalan H, Ulgen E, Yavuz T, Baranoski JF, Bozaykut A, Harmanci AS, Yalcin Y, Youngblood MW, Yasuno K, Bilgüvar K, Gunel M. ALPK3 gene mutation in a patient with congenital cardiomyopathy and dysmorphic features. Cold Spring Harb Mol Case Stud. 2017 Sep 1;3(5). pii: a001859. doi: 10.1101/mcs.a001859. Print 2017 Sep. PubMed PMID: 28630369; PubMed Central PMCID: PMC5593152.
15: Alatas I, Canaz H, Ozel K. Tethered cord release after fetal surgery. Childs Nerv Syst. 2017 Jun;33(6):889-890. doi: 10.1007/s00381-017-3416-z. Epub 2017 Apr 25. PubMed PMID: 28444461.
16: Aydın S, Canaz H, Erdogan ET, Durmaz N, Topcular B. Holmes' Tremor with Shoulder Pain Treated by Deep Brain Stimulation of Unilateral Ventral Intermediate Thalamic Nucleus and Globus Pallidus Internus. J Mov Disord. 2017 May;10(2):92-95. doi: 10.14802/jmd.16051. Epub 2017 Apr 18. PubMed PMID: 28415166; PubMed Central PMCID: PMC5435830.
17: Kilincaslan A, Aydin S, Kok BE, Akcakaya H, Yapici Z. Pallidal Stimulation in an 11-Year-Old Boy with Treatment-Resistant Tourette Syndrome. J Child Adolesc Psychopharmacol. 2017 Sep;27(7):673-674. doi: 10.1089/cap.2017.0008. Epub 2017 Mar 30. PubMed PMID: 28358600.
18: Sgourdou P, Mishra-Gorur K, Saotome I, Henagariu O, Tuysuz B, Campos C, Ishigame K, Giannikou K, Quon JL, Sestan N, Caglayan AO, Gunel M, Louvi A. Disruptions in asymmetric centrosome inheritance and WDR62-Aurora kinase B interactions in primary microcephaly. Sci Rep. 2017 Mar 8;7:43708. doi: 10.1038/srep43708. PubMed PMID: 28272472; PubMed Central PMCID: PMC5341122.
19: Gabor L, Canaz H, Canaz G, Kara N, Alatas I, Bozkus H. Russell-Silver syndrome associated with low conus medullaris. J Pediatr Neurosci. 2016 Oct-Dec;11(4):361-363. doi: 10.4103/1817-1745.199482. PubMed PMID: 28217167; PubMed Central PMCID: PMC5314858.
20: Lardelli RM, Schaffer AE, Eggens VR, Zaki MS, Grainger S, Sathe S, Van Nostrand EL, Schlachetzki Z, Rosti B, Akizu N, Scott E, Silhavy JL, Heckman LD, Rosti RO, Dikoglu E, Gregor A, Guemez-Gamboa A, Musaev D, Mande R, Widjaja A, Shaw TL, Markmiller S, Marin-Valencia I, Davies JH, de Meirleir L, Kayserili H, Altunoglu U, Freckmann ML, Warwick L, Chitayat D, Blaser S, Çağlayan AO, Bilguvar K, Per H, Fagerberg C, Christesen HT, Kibaek M, Aldinger KA, Manchester D, Matsumoto N, Muramatsu K, Saitsu H, Shiina M, Ogata K, Foulds N, Dobyns WB, Chi NC, Traver D, Spaccini L, Bova SM, Gabriel SB, Gunel M, Valente EM, Nassogne MC, Bennett EJ, Yeo GW, Baas F, Lykke-Andersen J, Gleeson JG. Biallelic mutations in the 3' exonuclease TOE1 cause pontocerebellar hypoplasia and uncover a role in snRNA processing. Nat Genet. 2017 Mar;49(3):457-464. doi: 10.1038/ng.3762. Epub 2017 Jan 16. PubMed PMID: 28092684; PubMed Central PMCID: PMC5325768.
21: Kaptan H, Kulaksızoğlu H, Kasımcan Ö, Seçkin B. The Association between Urinary Incontinence and Low Back Pain and Radiculopathy in Women. Open Access Maced J Med Sci. 2016 Dec 15;4(4):665-669. doi: 10.3889/oamjms.2016.129. Epub 2016 Nov 30. PubMed PMID: 28028410; PubMed Central PMCID: PMC5175518.
22: Gabor L, Canaz H, Canaz G, Kara N, Gulec EY, Alatas I. Foramina parietalia permagna: familial and radiological evaluation of two cases and review of literature. Childs Nerv Syst. 2017 May;33(5):853-857. doi: 10.1007/s00381-016-3315-8. Epub 2016 Dec 14. Review. PubMed PMID: 27975139.
23: Tărlungeanu DC, Deliu E, Dotter CP, Kara M, Janiesch PC, Scalise M, Galluccio M, Tesulov M, Morelli E, Sonmez FM, Bilguvar K, Ohgaki R, Kanai Y, Johansen A, Esharif S, Ben-Omran T, Topcu M, Schlessinger A, Indiveri C, Duncan KE, Caglayan AO, Gunel M, Gleeson JG, Novarino G. Impaired Amino Acid Transport at the Blood Brain Barrier Is a Cause of Autism Spectrum Disorder. Cell. 2016 Dec 1;167(6):1481-1494.e18. doi: 10.1016/j.cell.2016.11.013. PubMed PMID: 27912058; PubMed Central PMCID: PMC5554935.
24: Canaz H, Canaz G, Ucar BY, Alatas I. Hemimetameric shift in spina bifida: three case reports. Childs Nerv Syst. 2017 Mar;33(3):535-539. doi: 10.1007/s00381-016-3292-y. Epub 2016 Nov 7. PubMed PMID: 27822764.
25: Jerber J, Zaki MS, Al-Aama JY, Rosti RO, Ben-Omran T, Dikoglu E, Silhavy JL, Caglar C, Musaev D, Albrecht B, Campbell KP, Willer T, Almuriekhi M, Çağlayan AO, Vajsar J, Bilgüvar K, Ogur G, Abou Jamra R, Günel M, Gleeson JG. Biallelic Mutations in TMTC3, Encoding a Transmembrane and TPR-Containing Protein, Lead to Cobblestone Lissencephaly. Am J Hum Genet. 2016 Nov 3;99(5):1181-1189. doi: 10.1016/j.ajhg.2016.09.007. Epub 2016 Oct 20. PubMed PMID: 27773428; PubMed Central PMCID: PMC5097947.
26: Hanımoğlu H, Başlar Z. Intradiploic Hematoma in a Hemophilic Patient: Hemophilic Pseudotumor of Calvarium. Turk J Haematol. 2017 Mar 1;34(1):113-114. doi: 10.4274/tjh.2016.0254. Epub 2016 Sep 9. PubMed PMID: 27610826; PubMed Central PMCID: PMC5451677.
27: Sengul T, Saracoglu A, Sener S, Bezen O. The use of sugammadex in a pregnant patient with Wolff-Parkinson-White syndrome. J Clin Anesth. 2016 Sep;33:1-4. doi: 10.1016/j.jclinane.2015.12.023. Epub 2016 Apr 6. PubMed PMID: 27555124.
28: Li H, Bielas SL, Zaki MS, Ismail S, Farfara D, Um K, Rosti RO, Scott EC, Tu S, Chi NC, Gabriel S, Erson-Omay EZ, Ercan-Sencicek AG, Yasuno K, Çağlayan AO, Kaymakçalan H, Ekici B, Bilguvar K, Gunel M, Gleeson JG. Biallelic Mutations in Citron Kinase Link Mitotic Cytokinesis to Human Primary Microcephaly. Am J Hum Genet. 2016 Aug 4;99(2):501-10. doi: 10.1016/j.ajhg.2016.07.004. Epub 2016 Jul 21. PubMed PMID: 27453578; PubMed Central PMCID: PMC4974110.
29: Dilmen OK, Akcil EF, Tunali Y, Karabulut ES, Bahar M, Altindas F, Vehid H, Yentur E. Postoperative analgesia for supratentorial craniotomy. Clin Neurol Neurosurg. 2016 Jul;146:90-5. doi: 10.1016/j.clineuro.2016.04.026. Epub 2016 May 4. PubMed PMID: 27164511.
30: Özgenç MM, Çevik S, Soyalp C, Hanımoğlu H, Bektaş AF. Spontaneously rapid and complete resolution of acute subdural hemorrhage in a 1-year-old patient. Am J Emerg Med. 2016 Oct;34(10):2056.e1-2056.e4. doi: 10.1016/j.ajem.2016.03.028. Epub 2016 Mar 11. PubMed PMID: 27073137.
31: Kahraman S, Karadereler S, Cobanoglu M, Yilar S, Mutlu A, Ulusoy LO, Hamzaoglu A. Does pedicle screw fixation under age 5 cause spinal canal narrowing? A CT study with minimum 5 years follow-up. Eur Spine J. 2016 Jun;25(6):1665-73. doi: 10.1007/s00586-016-4484-6. Epub 2016 Mar 21. PubMed PMID: 27001135.
32: Genç G, Apaydın H, Gündüz A, Poyraz Ç, Oğuz S, Yağcı S, Canaz H, Aydın S, Gündoğdu-Eken A, Başak AN, Ertan S. Successful treatment of Juvenile parkinsonism with bilateral subthalamic deep brain stimulation in a 14-year-old patient with parkin gene mutation. Parkinsonism Relat Disord. 2016 Mar;24:137-8. doi: 10.1016/j.parkreldis.2016.01.018. Epub 2016 Jan 23. PubMed PMID: 26830385.
33: Çağlayan AO, Tüysüz B, Coşkun S, Quon J, Harmancı AS, Baranoski JF, Baran B, Erson-Omay EZ, Henegariu O, Mane SM, Bilgüvar K, Yasuno K, Günel M. A patient with a novel homozygous missense mutation in FTO and concomitant nonsense mutation in CETP. J Hum Genet. 2016 May;61(5):395-403. doi: 10.1038/jhg.2015.160. Epub 2016 Jan 7. PubMed PMID: 26740239; PubMed Central PMCID: PMC4880488.
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35: Toktaş ZO, Yılmaz B, Konya D, Yapıcıer O, Demir MK. Posterior epidural migration of lumbar disc fragment as an unusual ring-enhancing mass. Spine J. 2016 Feb;16(2):e31-2. doi: 10.1016/j.spinee.2015.09.026. Epub 2015 Sep 16. PubMed PMID: 26386172.
36: Demir MK, Yapıcıer Ö, Toktaş ZO, Yılmaz B, Akakın A, Konya D. Lumbar Paget disease with spinal stenosis and conus medullaris compression. Spine J. 2016 Jan 1;16(1):e51-2. doi: 10.1016/j.spinee.2015.09.010. Epub 2015 Sep 9. PubMed PMID: 26363247.
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38: Demir MK, Yapıcıer Ö, Toktaş ZO, Akakın A, Yılmaz B, Konya D. Ossified-calcified intradural and extradural thoracic spinal meningioma with neural foraminal extension. Spine J. 2016 Jan 1;16(1):e35-7. doi: 10.1016/j.spinee.2015.08.053. Epub 2015 Aug 31. PubMed PMID: 26334230.
39: Alatas I, Demirci H, Canaz H, Akdemir O, Baydin S, Ozel K. The role of urodynamic studies in the diagnosis and treatment of patients with spina bifida. Asian J Neurosurg. 2015 Apr-Jun;10(2):83-6. doi: 10.4103/1793-5482.154872. PubMed PMID: 25972935; PubMed Central PMCID: PMC4421973.
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