Associated Papers
Clinical and Biochemical Characteristics of Pseudohypoaldosteronism Type 1 with and Without Genetic Mutations: A Literature Review.
Nakata Y et al.
Journal of Clinical Medicine, 2025
40648780 (PubMed )
Supplement: jcm-14-04408-s001.zip › supplementary_file › supplementary_table_3__ENaC_group_.xlsx › ENaC_group_n_54_
Pulmonary manifestations of Pseudohypoaldosteronism type 1b: A systematic review of the literature.
Chantzaras AP et al.
Paediatric Respiratory Reviews, 2025
Case Report: A Novel Compound Heterozygote Mutation of the SCNN1B Gene Identified in a Chinese Familial Pseudohypoaldosteronism Disease Type I With Persistent Hyperkalemia.
Liu Z et al.
Frontiers in Pediatrics, 2022
Clinical Management in Systemic Type Pseudohypoaldosteronism Due to SCNN1B Variant and Literature Review
Karacan Küçükali G et al.
Journal of Clinical Research in Pediatric Endocrinology, 2021
Pseudohypoaldosteronism type 1 due to novel variants of SCNN1B gene.
Nobel YR et al.
Endocrinology, Diabetes & Metabolism Case Reports, 2016
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