A review of clinical characteristics and genetic backgrounds in Alport syndrome-Reference-Cited by-同舟云学术

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A review of clinical characteristics and genetic backgrounds in Alport syndrome

Published:2018-08-20 Issue:2 Volume:23 Page:158-168
ISSN:1342-1751
Container-title:Clinical and Experimental Nephrology
language:en
Short-container-title:Clin Exp Nephrol

Author:

Nozu Kandai^ORCID,Nakanishi Koichi,Abe Yoshifusa,Udagawa Tomohiro,Okada Shinichi,Okamoto Takayuki,Kaito Hiroshi,Kanemoto Katsuyoshi,Kobayashi Anna,Tanaka Eriko,Tanaka Kazuki,Hama Taketsugu,Fujimaru Rika,Miwa Saori,Yamamura Tomohiko,Yamamura Natsusmi,Horinouchi Tomoko,Minamikawa Shogo,Nagata Michio,Iijima Kazumoto

Funder

Ministry of Health, Labour and Welfare

Japan Agency for Medical Research and Development

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Springer Science and Business Media LLC

Subject

Physiology (medical),Nephrology,Physiology

Link

http://link.springer.com/article/10.1007/s10157-018-1629-4/fulltext.html

Reference48 articles.

1. Kashtan CE. Alport syndrome. An inherited disorder of renal, ocular, and cochlear basement membranes. Medicine (Baltimore). 1999;78(5):338–60.

2. Nakanishi K, Yoshikawa N, Iijima K, Kitagawa K, Nakamura H, Ito H, et al. Immunohistochemical study of alpha 1–5 chains of type IV collagen in hereditary nephritis. Kidney Int. 1994;46(5):1413–21.

3. Rheault MN, Kashtan CE. Inherited glomerular diseases. Ped Nephrol. 2016; 7 1918–84.

4. Mallett A, Tang W, Clayton PA, Stevenson S, McDonald SP, Hawley CM, et al. End-stage kidney disease due to Alport syndrome: outcomes in 296 consecutive Australia and New Zealand dialysis and transplant registry cases. Nephrol Dial Transplant. 2014;29(12):2277–86. https://doi.org/10.1093/ndt/gfu254 .

5. Hattori M, Sako M, Kaneko T, Ashida A, Matsunaga A, Igarashi T, et al. End-stage renal disease in Japanese children: a nationwide survey during 2006–2011. Clin Exp Nephrol. 2015;19(5):933–8. https://doi.org/10.1007/s10157-014-1077-8 .

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