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...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Sumida, Keiichi, Ubara, Yoshifumi, Hoshino, Junichi, Hayami, Noriko, Suwabe, Tatsuya, Hiramatsu, Rikako, Hasegawa, Eiko, Yamanouchi, Masayuki, Sawa, Naoki, Takaichi, Kenmei, Ohashi, Kenichi
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2013
Témata:
Case Report
On-line přístup: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
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky