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

Episodic movement disorders: from phenotype to genotype and back.

Current neurology and neuroscience reports - 1 Oct 2013

Brockmann Knut

Abstract excerpt

Episodic dyskinetic movement disorders are a heterogeneous group of rare conditions. Paroxysmal dyskinesias constitute the core of this group and usually exhibit normal interepisodic neurologic findings. Contrariwise, episodic dyskinesias occur as a particular feature of complex chronic neurologic disorders. Conjunction of accurate phenotyping with up-to-date methods of molecular genetics recently provided...

Read the complete abstract on PubMed

Topics

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

Share to PRRT2 gene
Share to Genotype
Share to Membrane Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Movement Disorders

Share to Nerve Tissue Proteins

Share to Phenotype

Share to Sodium-Potassium-Exchanging ATPase

Source

Identifiers

PMID: 23963607
DOI: 10.1007/s11910-013-0379-7

Genes

PRRT2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Episodic movement disorders: from phenotype to genotype and back.PMID 23963607Read ↗

Clinical and Genetic Overview of Paroxysmal Movement Disorders and Episodic Ataxias.Semantic proximity Read ↗

Phenotypes, genotypes, and the management of paroxysmal movement disorders.Semantic proximity Read ↗

Paroxysmal Genetic Movement Disorders and EpilepsySemantic proximity Read ↗

Paroxysmal movement disorders – practical update on diagnosis and managementSemantic proximity Read ↗

Paroxysmal Movement DisordersSemantic proximity Read ↗

Paroxysmal movement disorders: An update.Semantic proximity Read ↗

PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine.Semantic proximity Read ↗

Episodic neurologic disorders: syndromes, genes, and mechanisms.Semantic proximity Read ↗

Emerging Monogenic Complex Hyperkinetic Disorders.Semantic proximity Read ↗

Unravelling of the paroxysmal dyskinesiasSemantic proximity Read ↗

The clinical and genetic heterogeneity of paroxysmal dyskinesias.Semantic proximity Read ↗

Alternating hemiplegia of childhood: a distinct clinical entity and ATP1A3-related disorders: A narrative review.Semantic proximity Read ↗

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