Severe systemic type 1 pseudohypoaldosteronism: 5 years of evolution
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Reference9 articles.
1. A salt wasting syndrome in infancy;Cheek;Arch Dis Child,1958
2. Type I pseudohypoaldosteronism includes two clinically and genetically distinct entities with either renal or multiple target organ defects;Hanukoglu;J Clin Endocrinol Metab,1991
3. Disturbances of Na/K balance: pseudohypoaldosteronism revisited;Bonny;J Am Soc Nephrol,2002
4. A case of systemic pseudohypoaldosteronism with a novel mutation in the SCNN1A gene;Silva;Endocrinol Nutr,2013
5. Pulmonary epithelial sodium-cannel dysfunction and excess airway liquid in pseudohypoaldosteronism;Kerem;N Engl J Med,1999
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1. Pulmonary manifestations of Pseudohypoaldosteronism type 1b: A systematic review of the literature;Paediatric Respiratory Reviews;2024-09
2. Clinical Manifestations of Pseudohypoaldosteronism with Genotype-phenotype Correlation. A Single Center Experience, A Retrospective Cohort Study.;2024-04-18
3. Pseudohypoaldosteronism Type 1B and Cohen Syndrome: Novel Mutation, Unusual Combination, and Presentation;Cureus;2024-03-29
4. A case of severe systemic type 1 pseudohypoaldosteronism with 10 years of evolution;Journal of Pediatric Endocrinology and Metabolism;2022-08-02
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