Brain Arteriovenous Malformations associated with Hereditary Hemorrhagic Telangiectasia: Gene-Phenotype Correlations

Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant genetic disease with a wide spectrum of vascular malformations involving multiple organs. Nine-16% of patients with HHT harbor brain arteriovenous malformations (AVMs), which can cause intracranial hemorrhage. Our objective was to...

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書誌詳細
主要な著者: Nishida, Takeo, Faughnan, Marie E., Krings, Timo, Chakinala, Murali, Gossage, James R., Young, William L., Kim, Helen, Pourmohamad, Tony, Henderson, Katharine J., Schrum, Stacy D., James, Melissa, Quinnine, Nancy, Bharatha, Aditya, terBrugge, Karel G., White, Robert I.
フォーマット: Artigo
言語:Inglês
出版事項: 2012
主題:
Article
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3610331/
https://ncbi.nlm.nih.gov/pubmed/22991266
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.35622
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