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Endothelial dysfunction occurs prior to clinical evidence of Polycystic Kidney Disease
OBJECTIVE: Polycystic kidney disease (PKD), a monogenic disease with an autosomal dominant or an autosomal recessive form of inheritance (ARPKD), is the most common genetic cause of renal dysfunction and end stage renal failure. In addition to the development of cysts, the autosomal form of PKD is a...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3835344/ https://ncbi.nlm.nih.gov/pubmed/24008943 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000354236 |
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