Literature DB >> 35369019

Persistent Isolated Hematuria in a Japanese Woman.

Masayo Sato1, Toshio Mochizuki1,2, Kosaku Nitta1.   

Abstract

Entities:  

Keywords:  Alport syndrome; electron microscopy; glomerular and tubulointerstitial diseases; glomerular basement membrane; kidney biopsy; thin basement membrane nephropathy; type IV collagen

Mesh：

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Year:  2021        PMID： 35369019      PMCID： PMC8786000          DOI： 10.34067/KID.0005642020

Source DB:  PubMed          Journal:  Kidney360        ISSN： 2641-7650


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  3 in total

Review 1.  Alport syndrome--clinical phenotypes, incidence, and pathology.

Authors:  M C Gregory; D A Terreros; D F Barker; P N Fain; J C Denison; C L Atkin
Journal:  Contrib Nephrol       Date:  1996       Impact factor: 1.580

2.  Autosomal dominant form of type IV collagen nephropathy exists among patients with hereditary nephritis difficult to diagnose clinicopathologically.

Authors:  Aya Imafuku; Kandai Nozu; Naoki Sawa; Eiko Hasegawa; Rikako Hiramatsu; Masahiro Kawada; Junichi Hoshino; Kiho Tanaka; Yasuo Ishii; Kenmei Takaichi; Takeshi Fujii; Kenichi Ohashi; Kazumoto Iijima; Yoshifumi Ubara
Journal:  Nephrology (Carlton)       Date:  2018-10       Impact factor: 2.506

3.  Glomerular Basement Membrane Protein Expression and the Diagnosis and Prognosis of Autosomal Dominant Alport Syndrome.

Authors:  Taro Akihisa; Masayo Sato; Yoshie Wakayama; Sekiko Taneda; Shigeru Horita; Orie Hirose; Shiho Makabe; Hiroshi Kataoka; Takayasu Mori; Eisei Sohara; Shinichi Uchida; Kosaku Nitta; Toshio Mochizuki
Journal:  Kidney Med       Date:  2019-08-20
  3 in total

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