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Tolvaptan treatment for severe neonatal autosomal-dominant polycystic kidney disease
BACKGROUND: Severe neonatal autosomal-dominant polycystic kidney disease (ADPKD) is rare and easily confused with recessive PKD. Managing such infants is difficult and often unsuccessful. CASE DIAGNOSIS/TREATMENT: A female infant with massive renal enlargement, respiratory compromise and hyponatraem...
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| Publicado no: | Pediatr Nephrol |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Berlin Heidelberg
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5368203/ https://ncbi.nlm.nih.gov/pubmed/28194574 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00467-017-3584-9 |
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