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Last Updated: 03/06/2025
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Found 730 publications
A Rare Cause of Neonatal Salt Wasting Syndrome: Clinical Management of a Case Diagnosed with Pseudohypoaldosteronism Due to a Novel Homozygous Variant in the SCNN1B Gene.
Journal: Journal of clinical research in pediatric endocrinology
Published: December 26, 2024
Hyperkalaemic acidosis: blood pressure is the diagnostic clue.
Journal: Pediatric nephrology (Berlin, Germany)
Published: September 30, 2024
Prevalence of Hyperkalemia and Familial Hyperkalemic Hypertension in 5100 Patients Referred to a Tertiary Hypertension Unit.
Journal: Hypertension (Dallas, Tex. : 1979)
Published: September 04, 2024
Distal convoluted tubule-specific disruption of the COP9 signalosome but not its regulatory target cullin 3 causes tubular injury.
Journal: American journal of physiology. Renal physiology
Published: August 29, 2024
Renal pseudohypoaldosteronism type 1-an adult case series including a novel gene variant.
Journal: Endocrine
Published: August 16, 2024
Pulmonary manifestations of Pseudohypoaldosteronism type 1b: A systematic review of the literature.
Journal: Paediatric respiratory reviews
Published: August 05, 2024
An unusual case of Pseudohypoaldosteronism coexisting with cystic fibrosis.
Journal: BMJ case reports
Published: June 24, 2024
Autosomal Dominant Pseudohypoaldosteronism Type 1 in a Newborn With Failure to Thrive.
Journal: Cureus
Published: April 30, 2024
Pseudohypoaldosteronism type II and sensory neuropathy associated with a heterozygous pathogenic variant in KLHL3 gene, a case report.
Journal: Heliyon
Published: March 27, 2024
Last Updated: 03/06/2025