Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Liddle syndrome: genetics and mechanisms of Na+ channel defects.

The American journal of the medical sciences - 1 Dec 2001

Warnock D G

Abstract excerpt

Our current understanding of Na+ transport defects has been greatly expanded over the last several years and has provided new insights into unusual clinical syndromes resulting from mutations of specific ion transporters. These genetic disorders affect Na+ balance, with both Na+ retaining and Na+ wasting conditions being the consequence. A major focus of these studies has been the epithelial sodium channel...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Genetic Linkage
Share to Epithelial Sodium Channels
Share to Hyperaldosteronism

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hypertension

Share to Pseudohypoaldosteronism

Share to Sodium Channels

Share to Syndrome

Source

Identifiers

PMID: 11780687
DOI: 10.1097/00000441-200112000-00002

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Liddle syndrome: genetics and mechanisms of Na+ channel defects.PMID 11780687Read ↗

The epithelial sodium channel in hypertension.Semantic proximity Read ↗

Syndromes of impaired ion handling in the distal nephron: pseudohypoaldosteronism and familial hyperkalemic hypertension.Semantic proximity Read ↗

Liddle's syndrome: genetics and mechanisms of Na+ channel defects.Semantic proximity Read ↗

Aldosterone-related genetic effects in hypertension.Semantic proximity Read ↗

Pseudohypoaldosteronism: mutation found, problem solved?Semantic proximity Read ↗

Mendelian Forms of Human Hypertension and Mechanisms of DiseaseSemantic proximity Read ↗

Epithelial sodium channel, salt intake, and hypertension.Semantic proximity Read ↗

Mechanisms of type I and type II pseudohypoaldosteronism.Semantic proximity Read ↗

The ENaC channel as the primary determinant of two human diseases: Liddle syndrome and pseudohypoaldosteronism.Semantic proximity Read ↗

Inherited sodium avid states.Semantic proximity Read ↗

Reverse Phenotypes of Patients with Genetically Confirmed Liddle Syndrome.Semantic proximity Read ↗

Disorders of aldosterone synthesis, secretion, and cellular function.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.