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
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
Novel mutations in epithelial sodium channel (ENaC) subunit genes and phenotypic expression of multisystem pseudohypoaldosteronism.
Edelheit O et al.
Clinical Endocrinology, 2005
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