Clinical and genetic findings in children with central nervous system arteriovenous fistulas-Reference-Cited by-同舟云学术

Clinical and genetic findings in children with central nervous system arteriovenous fistulas

Published:2017-12 Issue:6 Volume:82 Page:972-980
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Saliou Guillaume¹²,Eyries Mélanie³⁴,Iacobucci Marta²,Knebel Jean‐François⁵,Waill Marie‐Christine³,Coulet Florence³,Ozanne Augustin²,Soubrier Florent³⁴

Affiliation:

1. Department of NeuroradiologyCentre Hospitalier Universitaire VaudoisLausanne Switzerland

2. Department of NeuroradiologyBicêtre HospitalLe Kremlin Bicêtre France

3. Department of geneticsHopital Pitié‐SalpêtrièreParis France

4. UMR‐S 1166‐ICAN; INSERM and UPMC Sorbonne UniversityParis France

5. département de Radiologie, Centre d'Imagerie Biomédicale, Hôpital Nestlé, CHUVLausanne Switzerland

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ana.25106

Reference42 articles.

1. Hereditary Hemorrhagic Telangiectasia

2. Capillary Malformation–Arteriovenous Malformation, a New Clinical and Genetic Disorder Caused by RASA1 Mutations

3. Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2

4. Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1

5. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome)

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