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

Familial pure paroxysmal kinesigenic dyskinesia in Han population from the Chinese mainland: a new subtype?

Epilepsy research - 1 Aug 2008

Zhou Jinxia, Li Guoliang, Chen Chanjuan, Liu Ding, Xiao Bo

Abstract excerpt

Paroxysmal kinesigenic dyskinesia (PKD) is a rare neurologic inherited disease with heterogeneity. Autosomal dominant (AD) is the common inherited mode. There have been two loci mapped to 16 chromosome for PKD. However, no gene responsible for it has been identified so far. We collected 6 pedigrees from Chinese mainland. There were 122 members in all, including 26 affected. According to New diagnostic criteria of...

Read the complete abstract on PubMed

Topics

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

Share to Aged, 80 and over
Share to Asian People
Share to Chorea

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 16

Share to Family Health

Share to Genes, Dominant

Share to Genetic Linkage

Share to Genetic Predisposition to Disease

Source

Identifiers

PMID: 18541410
DOI: 10.1016/j.eplepsyres.2008.04.012

Genes

NPL

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

Familial pure paroxysmal kinesigenic dyskinesia in Han population from the Chinese mainland: a new subtype?PMID 18541410Read ↗

A case of familial paroxysmal nonkinesigenic dyskinesia due to mutation of the PNKD gene in Chinese Mainland.Semantic proximity Read ↗

Paroxysmal kinesigenic dyskinesia: clinical report of 10 cases from three pedigrees with literature review.Semantic proximity Read ↗

Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene.Semantic proximity Read ↗

Clinical and Genetic Characteristics of Paroxysmal Kinesigenic Dyskinesia: A Single-Center Study and Literature Review.Semantic proximity Read ↗

Paroxysmal dyskinesias revisited: a review of 500 genetically proven cases and a new classification.Semantic proximity Read ↗

[Clinical manifestations and genetic diagnosis of paroxysmal kinesigenic dyskinesia].Semantic proximity Read ↗

A gene for familial paroxysmal dyskinesia (FPD1) maps to chromosome 2q.Semantic proximity Read ↗

Familial paroxysmal kinesigenic dyskinesia with a novel missense variant (Arg2866Trp) in NBEA.Semantic proximity Read ↗

Paroxysmal dyskinesiasSemantic proximity Read ↗

A locus for paroxysmal kinesigenic dyskinesia maps to human chromosome 16Semantic proximity Read ↗

[Clinical features and PRRT2 gene mutation in paroxysmal kinesigenic dyskinesia].Semantic proximity Read ↗

Mutation Analysis of MR-1, SLC2A1, and CLCN1 in 28 PRRT2-negative Paroxysmal Kinesigenic Dyskinesia Patients.Semantic proximity Read ↗

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