Associated Papers
Pulmonary manifestations of Pseudohypoaldosteronism type 1b: A systematic review of the literature.
Chantzaras AP et al.
Paediatric Respiratory Reviews, 2025
A mild and transient form of autosomal recessive pseudohypoaldosteronism type 1 caused by a novel mutation in the SCNN1A gene.
Efthymiadou A et al.
American Journal of Physiology. Endocrinology and Metabolism, 2023
Pseudohypoaldosteronism type 1b in fraternal twins of a Chinese family: report of two cases and literature review.
Gao Z et al.
Archives of Endocrinology and Metabolism, 2023
Clinical features and molecular basis of pseudohypoaldosteronism type 1.
Tajima T et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology, 2017
Phenotypic variation of autosomal recessive pseudohypoaldosteronism type I: a case in point.
Kala Ahluwalia G et al.
Clinical Case Reports, 2014
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