Vasopressin Type 2 Receptor V88M Mutation: Molecular Basis of Partial and Complete Nephrogenic Diabetes Insipidus-Reference-Cited by-同舟云学术

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Vasopressin Type 2 Receptor V88M Mutation: Molecular Basis of Partial and Complete Nephrogenic Diabetes Insipidus

Published:2010 Issue:1 Volume:114 Page:p1-p10
ISSN:1660-2137
Container-title:Nephron Physiology
language:en
Short-container-title:Nephron Physiol

Author:

Bockenhauer Detlef,Carpentier Eric,Rochdi Driss,van’t Hoff W.,Breton Billy,Bernier Virginie,Bouvier Michel,Bichet Daniel G.

Publisher

S. Karger AG

Subject

Physiology (medical),Nephrology,General Medicine,Physiology

Cited by 51 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. Lithium-induced Nephrogenic Diabetes Insipidus with Efficacy of Desmopressin in Combination with Thiazide Diuretics and Non-steroidal Anti-inflammatory Drugs: A Case Report with a Review of the Literature;Internal Medicine;2023

2. Genetic basis of nephrogenic diabetes insipidus;Molecular and Cellular Endocrinology;2023-01

3. Diabetes Insipidus;Pediatric Kidney Disease;2023

4. Disorders of Fluid and Electrolyte Balance;Endocrinology;2023

5. Desmopressin responding female nephrogenic diabetes insipidus: a case report;Childhood Kidney Diseases;2022-12-09

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