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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | J Pediatr Genet |
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| Κύριος συγγραφέας: | |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Georg Thieme Verlag KG
2014
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| Θέματα: | |
| Διαθέσιμο Online: | 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 |
| Ετικέτες: |
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