Endoglin Deficiency Impairs Stroke Recovery

BACKGROUND AND PURPOSE: Endoglin (ENG) deficiency causes hereditary hemorrhagic telangiectasia-1 (HHT1) and impairs myocardial repair. Pulmonary arteriovenous malformations (AVM) in HHT1 patients are associated with a high incidence of paradoxical embolism in the cerebral circulation and ischemic br...

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Autors principals: Shen, Fanxia, Vincent, Degos, Chu, Pei-Lun, Han, Zhenying, Westbroek, Erick M., Choi, Eun-Jung, Marchuk, Douglas, Kim, Helen, Lawton, Michael T., Maze, Mervyn, Young, William L., Su, Hua
Format: Artigo
Idioma:Inglês
Publicat: 2014
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4118747/
https://ncbi.nlm.nih.gov/pubmed/24876084
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/STROKEAHA.114.005115
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