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

Voltage-gated potassium channelopathy: an expanding spectrum of clinical phenotypes.

BMJ case reports - 10 Jan 2013

Shribman Sam, Patani Rickie, Deeb Jacquie, Chaudhuri Abhijit

Abstract excerpt

Autoimmune voltage-gated potassium channelopathies represent a wide and expanding spectrum of neurological conditions. We present a case demonstrating the phenotypic heterogeneity of antivoltage-gated potassium channels (VGKC)-associated disorders. Such cases may easily be dismissed as functional...

Read the complete abstract on PubMed

Topics

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

Share to Channelopathies
Share to Phenotype
Share to Potassium Channels, Voltage-Gated

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Open in PubMed Open full text

Identifiers

PMID: 23314449
DOI: 10.1136/bcr-2012-007742
PMCID: PMC3603777

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23314449-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Voltage-gated potassium channelopathy: an expanding spectrum of clinical phenotypes.PMID 23314449Read ↗

Emerging psychiatric syndromes associated with antivoltage-gated potassium channel complex antibodies.Semantic proximity Read ↗

Neurological channelopathies.Semantic proximity Read ↗

Carbamazepine-responsive Double-Negative VGKC-Complex Antibody Isaac’s Syndrome – A Case Report and Literature ReviewSemantic proximity Read ↗

Pediatric anti-CaVα2δ Autoimmune Encephalitis: a case report and literature reviewSemantic proximity Read ↗

Differences and diversity of autoimmune-mediated encephalitis in 77 cases from a single tertiary care centerSemantic proximity Read ↗

Expanded phenotypes and outcomes among 256 LGI1/CASPR2-IgG-positive patients.Semantic proximity Read ↗

Anti-voltage-Gated Potassium Channel (VGKC) Antibodies and Acquired Neuromyotonia in Patients with Immune Dysregulation, Polyendocrinopathy, Enteropathy X-Lined (IPEX) Syndrome.Semantic proximity Read ↗

DPPX-IgG-associated CNS hyperexcitability overlapping with acquired neuromyotonia (Isaacs syndrome): a case reportSemantic proximity Read ↗

Psychiatric Phenotypes of Pediatric Patients With Seropositive Autoimmune Encephalitis.Semantic proximity Read ↗

A clinico-radiological phenotype of voltage-gated potassium channel complex antibody-mediated disorder presenting with seizures and basal ganglia changes.Semantic proximity Read ↗

Chronic inflammatory demyelinating polyradiculoneuropathy: update on clinical features, phenotypes and treatment options.Semantic proximity Read ↗

Fabry disease with atypical neurological presentation: report of a case.Semantic proximity Read ↗

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