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Association of HLA-DR and -DQ Genes with Familial Moyamoya Disease in Koreans

OBJECTIVE: Moyamoya disease (MMD) is an uncommon cerebrovascular disorder, characterized by progressive occlusion at the terminal portion of the internal carotid artery. Incidence of the disease is high in East Asia and familial MMD accounts for about 15% of the disease. Although the pathogenesis is...

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Detalhes bibliográficos
Main Authors: Hong, Seok Ho, Wang, Kyu-Chang, Kim, Seung-Ki, Cho, Byung-Kyu, Park, Myoung Hee
Formato: Artigo
Idioma:Inglês
Publicado em: The Korean Neurosurgical Society 2009
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2803272/
https://ncbi.nlm.nih.gov/pubmed/20062572
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3340/jkns.2009.46.6.558
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