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Autosomal dominant polycystic kidney disease: recent advances in clinical management
The first clinical descriptions of autosomal dominant polycystic kidney disease (ADPKD) go back at least 500 years to the late 16 (th) century. Advances in understanding disease presentation and pathophysiology have mirrored the progress of clinical medicine in anatomy, pathology, physiology, cell b...
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| Yayımlandı: | F1000Res |
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| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
F1000Research
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4991528/ https://ncbi.nlm.nih.gov/pubmed/27594986 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.9045.1 |
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