Intravenous and topical intranasal bevacizumab (Avastin) in hereditary hemorrhagic telangiectasia

Author:

Brinkerhoff Brian T.,Choong Nicholas W.,Treisman Jonathan S.,Poetker David M.

Publisher

Elsevier BV

Subject

Otorhinolaryngology

Reference11 articles.

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

2. Patients with hereditary hemorrhagic telangiectasia have increased plasma levels of vascular endothelial growth factor and transforming growth factor–beta1 as well as high ALK1 tissue expression;Sadick;Haematologica,2005

3. Dramatic improvement in hereditary hemorrhagic telangiectasia after treatment with the vascular endothelial growth factor (VEGF) antagonist bevacizumab;Flieger;Ann Hematol,2006

4. Bevacizumab in hereditary hemorrhagic telangiectasia;Bose;N Engl J Med,2009

5. Long-term therapy with bevacizumab in hereditary hemorrhagic telangiectasia;Brinkerhoff;N Engl J Med,2011

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