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Successful therapy with bevacizumab in a case of hereditary hemorrhagic telangiectasia
Hereditary hemorrhagic telangiectasia (HHT), genetic disorder manifested by uncontrolled multisystem angiogenesis with epistaxis, gastrointestinal bleeding, iron-deficiency anaemia, and arteriovenous malformations (AVM) is often related with increased levels of vascular endothelial growth factor (VE...
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| Foilsithe in: | Hum Vaccin Immunother |
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| Main Authors: | , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Taylor & Francis
2015
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4514147/ https://ncbi.nlm.nih.gov/pubmed/25839219 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/21645515.2015.1011960 |
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