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Myeloperoxidase-antineutrophil cytoplasmic antibody-associated crescentic glomerulonephritis in autosomal dominant polycystic kidney disease

BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is an inherited disorder that is characterized by the development of cysts in the kidneys and other organs. Urinary protein excretion is usually less than 1 g/day, and ADPKD is rarely associated with nephrotic syndrome or rapidly progr...

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Détails bibliographiques
Auteurs principaux: Sumida, Keiichi, Ubara, Yoshifumi, Hoshino, Junichi, Hayami, Noriko, Suwabe, Tatsuya, Hiramatsu, Rikako, Hasegawa, Eiko, Yamanouchi, Masayuki, Sawa, Naoki, Takaichi, Kenmei, Ohashi, Kenichi
Format: Artigo
Langue:Inglês
Publié: BioMed Central 2013
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3644260/
https://ncbi.nlm.nih.gov/pubmed/23617397
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2369-14-94
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