Show pageBacklinksCite current pageExport to PDFBack to top This page is read only. You can view the source, but not change it. Ask your administrator if you think this is wrong. ====== Pulmonary arterial hypertension ====== Pulmonary arterial hypertension (PAH) is one form of a broader condition known as pulmonary [[hypertension]], which is high blood pressure in the lungs. In PAH, this increased pressure in the vessels is caused by obstruction in the small arteries in the lung for a variety of reasons. ---- 1: Otero-Fernández P, Negreira-Caamaño M, Moreno-Flores A, Calvo-Alonso M, Sosa- Cabezas JP, Mateos-Romero A, Villena-Martín M. [[Pulmonary Arterial Hypertension]] due to [[Ventriculoatrial Shunt]]s: A [[Case Report]] and [[Literature Review]]. Neurochirurgie. 2022 Apr 21:S0028-3770(22)00061-3. doi: 10.1016/j.neuchi.2022.03.002. Epub ahead of print. PMID: 35461815. 2: Sundaram M, Mishra RK, Uppar AM. Neurogenic stunned myocardium resulting from surgical brainstem handling during resection of paediatric recurrent medulloblastoma-a possible brain heart interaction. Childs Nerv Syst. 2022 Apr 23. doi: 10.1007/s00381-022-05523-6. Epub ahead of print. PMID: 35460357. 3: He T, Zhang J, Qiao T, Zhang Z, Han H, Yang C, Chen Y, Ruan Y, Meng L. Compensatory roles of Protein Related to DAN and Cerberus (PRDC) decrease in pulmonary arterial hypertension. Int J Biol Sci. 2022 Mar 6;18(6):2372-2391. doi: 10.7150/ijbs.70247. PMID: 35414785; PMCID: PMC8990474. 4: Puk O, Nowacka A, Smulewicz K, Mocna K, Bursiewicz W, Kęsy N, Kwiecień J, Wiciński M. Pulmonary artery targeted therapy in treatment of COVID-19 related ARDS. Literature review. Biomed Pharmacother. 2022 Feb;146:112592. doi: 10.1016/j.biopha.2021.112592. Epub 2021 Dec 25. 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