Associated Papers
Liddle syndrome with a SCNN1B mutation: a case report and systematic review.
Tang Q et al.
Bmc Nephrology, 2025
A frameshift mutation in the SCNN1B gene in a family with Liddle syndrome: A case report and systematic review.
Lu Y et al.
Molecular Medicine Reports, 2024
38099339 (PubMed )
Supplement: Supplementary_Data.pdf
Genetic screening for monogenic hypertension in hypertensive individuals in a clinical setting.
Bao M et al.
Journal of Medical Genetics, 2020
Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Characterized by Early-Onset Hypertension.
Fan P et al.
American Journal of Hypertension, 2020
32161960 (PubMed )
Supplement: hpaa037_suppl_supplementary_table_s2.doc
A family with Liddle's syndrome caused by a new c.1721 deletion mutation in the epithelial sodium channel β-subunit.
Ding X et al.
Experimental and Therapeutic Medicine, 2019
Liddle Syndrome: Review of the Literature and Description of a New Case.
Tetti M et al.
International Journal of Molecular Sciences, 2018
Liddle syndrome: clinical and genetic profiles.
Cui Y et al.
Journal of Clinical Hypertension (greenwich, Conn.), 2017
Liddle syndrome in a Turkish family with heterogeneous phenotypes.
Büyükkaragöz B et al.
Pediatrics International : Official Journal of the Japan Pediatric Society, 2016
A novel epithelial sodium channel beta-subunit mutation associated with hypertensive Liddle syndrome.
Freundlich M et al.
Pediatric Nephrology (berlin, Germany), 2005
Genotype-phenotype analysis of a newly discovered family with Liddle's syndrome.
Jeunemaitre X et al.
Journal of Hypertension, 1997
Disorders of the epithelial Na(+) channel in Liddle's syndrome and autosomal recessive pseudohypoaldosteronism type 1.
Oh YS et al.
Experimental Nephrology, 0
Reversal of convention: from man to experimental animal in elucidating the function of the renal amiloride-sensitive sodium channel.
Hummler E
Experimental Nephrology, 0
Select a paper to view details