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 revisited: does it exist?

Annals of neurology - 1 Aug 2002

Chinnery Patrick F, Walls Timothy J, Hanna Michael G, Bates David, Fawcett Peter R W

Abstract excerpt

Normokalemic periodic paralysis (normoKPP) is well established in the literature, but there are doubts as to whether it exists as a discrete entity. Retrospective clinical and molecular analysis has confirmed suspicions that most normoKPP families actually have a variant of hyperkalemic periodic paralysis (hyperKPP) due to a mutation of the muscle-specific sodium channel gene (SCN4A). However, the original...

Read the complete abstract on PubMed

Topics

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

Share to Amino Acid Sequence
Share to Electromyography
Share to Genetic Variation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to NAV1.4 Voltage-Gated Sodium Channel

Share to Paralyses, Familial Periodic

Share to Potassium

Share to Reference Values

Share to Sodium Channels

Source

Identifiers

PMID: 12210802
DOI: 10.1002/ana.10257

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

Normokalemic periodic paralysis revisited: does it exist?PMID 12210802Read ↗

Normokalemic periodic paralysis is not a distinct disease.Semantic proximity Read ↗

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

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

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

Periodic paralysis.Semantic proximity Read ↗

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

[Screening SCN4A gene for mutations with denaturing high performance liquid chromatography technology in a Chinese family with normokalemic periodic paralysis].Semantic proximity Read ↗

An unusual pathologic feature and phenotype associated with familial hyperkalemic periodic paralysis.Semantic proximity Read ↗

[Normokalemic periodic paralysis lasting for two weeks: a severe form of sodium channelopathy with M1592V mutation].Semantic proximity Read ↗

Normokalemic periodic paralysis with involuntary movements and generalized epilepsy associated with two novel mutations in SCN4A gene.Semantic proximity Read ↗

Exercise test on the patients with normokalaemic periodic paralysis from a Chinese family with a mutation in the SCN4A gene.Semantic proximity Read ↗

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

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