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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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Detalhes bibliográficos
Main Authors: Sumida, Keiichi, Ubara, Yoshifumi, Hoshino, Junichi, Hayami, Noriko, Suwabe, Tatsuya, Hiramatsu, Rikako, Hasegawa, Eiko, Yamanouchi, Masayuki, Sawa, Naoki, Takaichi, Kenmei, Ohashi, Kenichi
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2013
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Acesso em linha: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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