Pseudohypoaldosteronism Type 1: The Presentation and Management of a Neonate With a Novel Mutation of the SCNN1B Gene Found in Two Hispanic Siblings-Reference-Cited by-同舟云学术

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Pseudohypoaldosteronism Type 1: The Presentation and Management of a Neonate With a Novel Mutation of the SCNN1B Gene Found in Two Hispanic Siblings

Published:2022-04-07 Issue: Volume: Page:
ISSN:2168-8184
Container-title:Cureus
language:en
Short-container-title:

Author:

Pugh Charles P

Publisher

Cureus, Inc.

Subject

Aerospace Engineering

Reference9 articles.

1. Clinical and molecular features of type 1 pseudohypoaldosteronism;Riepe FG;Horm Res,2009

2. Autosomal dominant pseudohypoaldosteronism type 1: mechanisms, evidence for neonatal lethality, and phenotypic expression in adults;Geller DS;JASN,2006

3. A salt wasting syndrome in infancy;Cheek DB;Arch Dis Child,1958

4. The mutational constraint spectrum quantified from variation in 141,456 humans;Karczewski KJ;Nature,2020

5. Pseudohypoaldosteronism in a neonate presenting as life-threatening hyperkalemia;Attia NA;Case Rep Endocrinol,2016

Cited by 2 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. Pulmonary manifestations of Pseudohypoaldosteronism type 1b: A systematic review of the literature;Paediatric Respiratory Reviews;2024-09

2. The Epithelial Sodium Channel—An Underestimated Drug Target;International Journal of Molecular Sciences;2023-04-24

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