European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT)

Hereditary haemorrhagic telangiectasia (HHT) is a multisystemic vascular dysplasia inherited as an autosomal dominant trait. Approximately 10 % of patients have cerebral vascular malformations, a proportion being cerebral arteriovenous malformations (AVMs) and fistulae that may lead to potentially d...

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書誌詳細
出版年:Orphanet J Rare Dis
主要な著者: Eker, Omer F., Boccardi, Edoardo, Sure, Ulrich, Patel, Maneesh C., Alicante, Saverio, Alsafi, Ali, Coote, Nicola, Droege, Freya, Dupuis, Olivier, Fialla, Annette Dam, Jones, Bryony, Kariholu, Ujwal, Kjeldsen, Anette D., Lefroy, David, Lenato, Gennaro M., Mager, Hans Jurgen, Manfredi, Guido, Nielsen, Troels H., Pagella, Fabio, Post, Marco C., Rennie, Catherine, Sabbà, Carlo, Suppressa, Patrizia, Toerring, Pernille M., Ugolini, Sara, Buscarini, Elisabetta, Dupuis-Girod, Sophie, Shovlin, Claire L.
フォーマット: Artigo
言語:Inglês
出版事項: BioMed Central 2020
主題:
Position Statement
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC7322871/
https://ncbi.nlm.nih.gov/pubmed/32600364
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-020-01386-9
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