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

Normokalemic periodic paralysis is not a distinct disease.

Muscle & nerve - 1 Dec 2012

Song Young-Wha, Kim Sung-Jo, Heo Tae-Hwe, Kim Man-Ho, Kim June-Bum

Abstract excerpt

INTRODUCTION: Recent molecular studies of the original cases of normokalemic periodic paralysis (normoKPP) have raised suspicions that these families actually had hyperkalemic periodic paralysis (hyperKPP) due to mutations in the skeletal muscle sodium channel gene SCN4A. However, there is still a debate about the existence of normoKPP. METHODS: We screened 230 individuals with primary periodic paralysis for...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Arginine
Share to DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Electrocardiography

Share to Family Health

Share to Glycine

Share to NAV1.4 Voltage-Gated Sodium Channel

Share to Paralyses, Familial Periodic

Source

Identifiers

PMID: 22926674
DOI: 10.1002/mus.23441

Genes

KCNJ2

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Normokalemic periodic paralysis is not a distinct disease.PMID 22926674Read ↗

Normokalemic periodic paralysis revisited: does it exist?Semantic proximity Read ↗

New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysisSemantic proximity Read ↗

The clinical and genetic heterogeneity analysis of five families with primary periodic paralysis.Semantic proximity Read ↗

Cardiac arrhythmias in hypokalemic periodic paralysis: Hypokalemia as only cause?Semantic proximity Read ↗

The primary periodic paralyses: diagnosis, pathogenesis and treatment.Semantic proximity Read ↗

[Clinical and molecular genetic analysis of a family with normokalemic periodic paralysis].Semantic proximity Read ↗

Identification of a SCN4A mutation in a large Chinese family with atypical normokalemic periodic paralysis using whole-exome sequencing.Semantic proximity Read ↗

Genotype and phenotype analysis of patients with sporadic periodic paralysis.Semantic proximity Read ↗

Thyrotoxic periodic paralysis associated with a mutation in the sodium channel gene SCN4A.Semantic proximity Read ↗

Sinus arrest in familial hypokalemic periodic paralysis caused by SCN4A mutation: a case report.Semantic proximity Read ↗

Mutations associated with hypokalemic periodic paralysis: from hotspot regions to complete analysis of CACNA1S and SCN4A genes.Semantic proximity Read ↗

A new clinical entity in T704M mutation in periodic paralysis.Semantic proximity Read ↗

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