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

Thyrotoxic periodic paralysis and polymorphisms of sodium-potassium ATPase genes.

Clinical endocrinology - 1 Feb 2006

Kung Annie W C, Lau K S, Cheung William M W, Chan Vivian

Abstract excerpt

OBJECTIVE: Thyrotoxic periodic paralysis (TPP) is a complication of hyperthyroidism association with recurrent, reversible episodes of muscle weakness. Increased sodium-potassium ATPase (Na/K-ATPase) pump activity is postulated to contribute to the hypokalaemic paralytic attacks in TPP. The aim of this study was to determine the genetic predisposition to TPP in relation to Na/K-ATPase genes. DESIGN: A...

Read the complete abstract on PubMed

Topics

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

Share to Adenosine Triphosphatases
Share to Cation Transport Proteins
Share to Cell Adhesion Molecules, Neuronal

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Graves Disease

Share to Haplotypes

Share to Hypokalemic Periodic Paralysis

Share to Protein Subunits

Share to Sodium-Potassium-Exchanging ATPase

Source

Identifiers

PMID: 16430714
DOI: 10.1111/j.1365-2265.2005.02442.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

Thyrotoxic periodic paralysis and polymorphisms of sodium-potassium ATPase genes.PMID 16430714Read ↗

A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis.Semantic proximity Read ↗

Thyrotoxic periodic paralysis: clinical and molecular aspects.Semantic proximity Read ↗

Association of KCNJ2 Genetic Variants with Susceptibility to Thyrotoxic Periodic Paralysis in Patients with Graves' Disease.Semantic proximity Read ↗

The clinical and genetic features in a cohort of mainland Chinese patients with thyrotoxic periodic paralysis.Semantic proximity Read ↗

Thyrotoxic Hypokalemic Periodic Paralysis: Pathophysiological Mechanisms.Semantic proximity Read ↗

Genetic variant rs623011 (17q24.3) associates with non-familial thyrotoxic and sporadic hypokalemic paralysis.Semantic proximity Read ↗

Genome-wide meta-analysis reveals novel susceptibility loci for thyrotoxic periodic paralysis.Semantic proximity Read ↗

Association of novel single nucleotide polymorphisms in the calcium channel alpha 1 subunit gene (Ca(v)1.1) and thyrotoxic periodic paralysis.Semantic proximity Read ↗

Skeletal muscle dihydropyridine-sensitive calcium channel (CACNA1S) gene mutations in chinese patients with hypokalemic periodic paralysis.Semantic proximity Read ↗

Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3.Semantic proximity Read ↗

Association of genetic variants in GABRA3 gene and thyrotoxic hypokalaemic periodic paralysis in Thai population.Semantic proximity Read ↗

Genetic Screening of Patients with Thyrotoxic Hypokalemic Periodic Paralysis: An Experience from a Tertiary Care Hospital in the Northeast of Brazil.Semantic proximity Read ↗

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