Bevacizumab for treating Hereditary Hemorrhagic Telangiectasia patients with severe hepatic involvement or refractory anemia

Author:

Vázquez CarolinaORCID,Gonzalez María Laura,Ferraris Augusto,Bandi Juan Carlos,Serra Marcelo MartínORCID

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference36 articles.

1. International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia;ME Faughnan;J Med Genet,2011

2. The prevalence and manifestations of hereditary hemorrhagic telangiectasia in the Afro-Caribbean population of the Netherlands Antilles: A family screening;CJJ Westermann;Am J Med Genet,2003

3. Serra MM, Franceschini C PJ. First prevalence report of hereditary hemorrhagic telangiectasia in a Latin American population. HHT International Scientific Conference 2015. Captiva, Florida, USA. Angiogenesis. 2015;18: 525–75.

4. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome);CL Shovlin;Am J Med Genet,2000

5. Diagnosis and management of gastrointestinal bleeding in patients with hereditary hemorrhagic telangiectasia;V. Longacre A;Am J Gastroenterol,2003

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