Treatment of Hereditary Hemorrhagic Telangiectasia–Related Epistaxis-Reference-Cited by-同舟云学术

Treatment of Hereditary Hemorrhagic Telangiectasia–Related Epistaxis

Published:2016-06 Issue:3 Volume:49 Page:639-654
ISSN:0030-6665
Container-title:Otolaryngologic Clinics of North America
language:en
Short-container-title:Otolaryngologic Clinics of North America

Author:

Sautter Nathan B.,Smith Timothy L.

Publisher

Elsevier BV

Subject

General Medicine,Otorhinolaryngology

Reference51 articles.

2. Patients with hereditary hemorrhagic telangiectasia have increased plasma levels of vascular endothelial growth factor and transforming growth factor-beta 1 as well as high ALK1 tissue expression;Sadick;Haematologica,2005

3. Distribution of ENG and ACVRL1 (ALK1) mutations in French HHT patients;Lesca;Hum Mutat,2006

4. A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4);Gallione;Lancet,2004

5. BMP9 mutations cause a vascular-anomaly syndrome with phenotypic overlap with hereditary hemorrhagic telangiectasia;Wooderchak-Donahue;Am J Hum Genet,2013

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