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Individualized therapy of HHT driven by network analysis of metabolomic profiles
BACKGROUND: Hereditary Hemorrhagic Telangiectasia (HHT) is an autosomal dominant disease with a varying range of phenotypes involving abnormal vasculature primarily manifested as arteriovenous malformations in various organs, including the nose, brain, liver, and lungs. The varied presentation and i...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3339509/ https://ncbi.nlm.nih.gov/pubmed/22185482 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1752-0509-5-200 |
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