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
Systemic Pseudohypoaldosteronism Type I: A Case Report and Review of the Literature.
Nur N et al.
Case Reports in Pediatrics, 2017
Five novel mutations in the SCNN1A gene causing autosomal recessive pseudohypoaldosteronism type 1.
Welzel M et al.
European Journal of Endocrinology, 2013
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