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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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Библиографические подробности
Главные авторы: Sumida, Keiichi, Ubara, Yoshifumi, Hoshino, Junichi, Hayami, Noriko, Suwabe, Tatsuya, Hiramatsu, Rikako, Hasegawa, Eiko, Yamanouchi, Masayuki, Sawa, Naoki, Takaichi, Kenmei, Ohashi, Kenichi
Формат: Artigo
Язык:Inglês
Опубликовано: BioMed Central 2013
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Online-ссылка: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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