Treatment of pulmonary hypertension in patients with Hereditary Hemorrhagic Telangiectasia – A case series and systematic review
Author:
Publisher
Elsevier BV
Subject
Pharmacology (medical),Biochemistry (medical),Pulmonary and Respiratory Medicine
Reference60 articles.
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2. Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1;McAllister;Nat. Genet.,1994
3. The activin receptor-like kinase 1 gene: genomic structure and mutations in hereditary hemorrhagic telangiectasia type 2;Berg;Am. J. Hum. Genet.,1997
4. International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia;Faughnan;J. Med. Genet.,2011
5. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome);Shovlin;Am. J. Med. Genet.,2000
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