Clinical and molecular characterization of a family with a dominant renin gene mutation and response to treatment with fludrocortisone-Reference-Cited by-同舟云学术

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Clinical and molecular characterization of a family with a dominant renin gene mutation and response to treatment with fludrocortisone

Published:2010-12-01 Issue:12 Volume:74 Page:411-422
ISSN:0301-0430
Container-title:Clinical Nephrology
language:en
Short-container-title:CN

Author:

Bleyer A.J.,Zivná M.,Hulková H.,Hodanová K.,Vyletal P.,Sikora J.,Zivný J.,Sovová J.,Hart T.C.,Adams J.N.,Elleder M.,Kapp K.,Haws R.,Cornell L.D.,Kmoch S.,Hart P.S.

Publisher

Dustri-Verlgag Dr. Karl Feistle

Subject

Nephrology,General Medicine

Cited by 41 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hypoaldosteronism due to a novel SEC61A1 variant successfully treated with fludrocortisone;Clinical Kidney Journal;2024-07-05

2. Case-inspired exploration of renin mutations in autosomal dominant tubulointerstitial kidney disease: not all paths lead to the endoplasmic reticulum;Pediatric Nephrology;2024-03-23

3. Two sides of the same coin: a complex presentation of autosomal dominant tubulointerstitial kidney diseases: a literature review and case reports;Frontiers in Pediatrics;2023-11-10

4. The contribution of the AT1 receptor to erythropoiesis;Biochemical Pharmacology;2023-11

5. Leader peptide or pro-segment mutants of renin are misrouted to mitochondria in autosomal dominant tubulointerstitial kidney disease;Disease Models & Mechanisms;2023-06-01

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