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Autosomal recessive polycystic kidney disease: The prototype of the hepato-renal fibrocystic diseases
Autosomal recessive polycystic kidney disease (ARPKD) is a severe, typically early onset form of renal cystic disease. The care of ARPKD patients has traditionally been the purview of pediatric nephrologists for management of systemic hypertension and progressive renal insufficiency. However, the di...
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| Publicado no: | J Pediatr Genet |
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| Autor principal: | |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Georg Thieme Verlag KG
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4306463/ https://ncbi.nlm.nih.gov/pubmed/25632369 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/PGE-14092 |
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