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Podocyturia: A Clue for the Rational Use of Amiloride in Alport Renal Disease
No specific or efficient treatment exists for Alport syndrome, an X-linked hereditary disease caused by mutations in collagen type IV, a crucial component of the glomerular basement membrane. Kidney failure is usually a major complication of the disease, and patients require renal replacement therap...
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| Publicat a: | Case Rep Nephrol |
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| Autors principals: | , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Hindawi Publishing Corporation
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4749773/ https://ncbi.nlm.nih.gov/pubmed/26942026 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2016/1492743 |
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