Collagenofibrotic Glomerulopathy-Reference-Cited by-同舟云学术

Collagenofibrotic Glomerulopathy

Published:2021-03-15 Issue:6 Volume:60 Page:911-915
ISSN:0918-2918
Container-title:Internal Medicine
language:en
Short-container-title:Intern. Med.

Author:

Miyake Masato¹,Katayama Kan²,Ehara Takashi³,Sado Yoshikazu⁴,Nawa Shunpei¹,Murata Tomohiro²,Mizutani Yasuhide¹,Joh Kensuke⁵,Ito Masaaki²,Dohi Kaoru²

Affiliation:

1. Department of Nephrology, Yokkaichi Hazu Medical Center, Japan

2. Department of Cardiology and Nephrology, Mie University Graduate School of Medicine, Japan

3. Department of Histopathology, Shinshu University School of Medicine, Japan

4. Division of Immunology, Shigei Medical Research Institute, Japan

5. Department of Pathology, The Jikei University School of Medicine, Japan

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

Link

https://www.jstage.jst.go.jp/article/internalmedicine/60/6/60_6090-20/_pdf

Reference13 articles.

1. 1. Alchi B, Nishi S, Narita I, Gejyo F. Collagenofibrotic glomerulopathy: clinicopathologic overview of a rare glomerular disease. Am J Kidney Dis 49: 499-506, 2007.

2. 2. Yoshioka K, Takemura T, Tohda M, et al. Glomerular localization of type III collagen in human kidney disease. Kidney Int 35: 1203-1211, 1989.

3. 3. Dombros N, Katz A. Nail patella-like renal lesions in the absence of skeletal abnormalities. Am J Kidney Dis 1: 237-240, 1982.

4. 4. Isojima T, Harita Y, Furuyama M, et al. LMX1B mutation with residual transcriptional activity as a cause of isolated glomerulopathy. Nephrol Dial Transplant 29: 81-88, 2014.

5. 5. Harita Y, Kitanaka S, Isojima T, Ashida A, Hattori M. Spectrum of LMX1B mutations: from nail-patella syndrome to isolated nephropathy. Pediatr Nephrol 32: 1845-1850, 2017.

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