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

Benefit of carbamazepine in a patient with hemiplegic migraine associated with PRRT2 mutation.

Developmental medicine and child neurology - 1 Sept 2014

Dale Russell C, Gardiner Alice, Branson Joceline A, Houlden Henry

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Analgesics, Non-Narcotic
Share to Carbamazepine
Share to Child
Share to Family

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Membrane Proteins

Share to Migraine with Aura

Share to Mutation

Share to Nerve Tissue Proteins

Source

Identifiers

PMID: 24506539
DOI: 10.1111/dmcn.12396

Genes

PRRT2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Benefit of carbamazepine in a patient with hemiplegic migraine associated with PRRT2 mutation.PMID 24506539Read ↗

PRRT2 and hemiplegic migraine: a complex association.Semantic proximity Read ↗

Functional characterization of a novel PRRT2 variant found in a Portuguese patient with hemiplegic migraine.Semantic proximity Read ↗

PRRT2 mutations cause hemiplegic migraine.Semantic proximity Read ↗

Hemiplegic Migraine Associated With PRRT2 Variations: A Clinical and Genetic Study.Semantic proximity Read ↗

PRRT2 mutation correlated with phenotype of paroxysmal kinesigenic dyskinesia and drug response.Semantic proximity Read ↗

PharmGKB summary: carbamazepine pathway.Semantic proximity Read ↗

Novel ATP1A3 mutation in a sporadic RDP patient with minimal benefit from deep brain stimulation.Semantic proximity Read ↗

Super-refractory status epilepticus related to COVID-19 in a paediatric patient with PRRT2 mutation.Semantic proximity Read ↗

Dihydropteridine Reductase Deficiency: A Treatable Neurotransmitter Movement Disorder Masquerading as Refractory Epilepsy Due to Novel Mutation.Semantic proximity Read ↗

Familial PRRT2 mutation with heterogeneous paroxysmal disorders including paroxysmal torticollis and hemiplegic migraine.Semantic proximity Read ↗

Hemiplegic migraine with reversible cerebral vasoconstriction caused by ATP1A2 mutations.Semantic proximity Read ↗

A case of familial hemiplegic migraine associated with a novel ATP1A2 gene mutation.Semantic proximity Read ↗

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