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

The neuronal channelopathies.

Brain : a journal of neurology - 1 Jun 2002

Kullmann Dimitri M

Abstract excerpt

This review addresses the molecular and cellular mechanisms of diseases caused by inherited mutations of ion channels in neurones. Among important recent advances is the elucidation of several dominantly inherited epilepsies caused by mutations of both voltage-gated and ligand-gated ion channels. The neuronal channelopathies show evidence of phenotypic convergence; notably, episodic ataxia can be caused by...

Read the complete abstract on PubMed

Topics

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

Share to Central Nervous System Diseases
Share to Ion Channels
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 12023309
DOI: 10.1093/brain/awf130

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

The neuronal channelopathies.PMID 12023309Read ↗

Neurological ChannelopathiesSemantic proximity Read ↗

Genetic neurological channelopathies.Semantic proximity Read ↗

The inherited episodic ataxias: how well do we understand the disease mechanisms?Semantic proximity Read ↗

Neurological disorders caused by inherited ion-channel mutations.Semantic proximity Read ↗

Neurological channelopathies.Semantic proximity Read ↗

Genetic neurological channelopathies: molecular genetics and clinical phenotypes.Semantic proximity Read ↗

Mutational consequences of aberrant ion channels in neurological disorders.Semantic proximity Read ↗

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

Neurological channelopathies: new insights into disease mechanisms and ion channel functionSemantic proximity Read ↗

Genetic paroxysmal neurological disorders featuring episodic ataxia and epilepsy.Semantic proximity Read ↗

Ion channel mutations in neuronal diseases: a genetics perspective.Semantic proximity Read ↗

Channelopathies: ion channel defects linked to heritable clinical disorders.Semantic proximity Read ↗

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