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

Hemiplegic migraine type 2 with new mutation of the ATP1A2 gene in Japanese cases.

Neuroscience research - 1 Jul 2022

Oda Ituki, Danno Daisuke, Saigoh Kazumasa, Wolf Johanna, Kawashita Norihito, Hirano Makito, Samukawa Makoto, Kitamura Shigekazu, Kikui Shoji, Takeshima Takao, Mitsui Yoshiyuki, Kusunoki Susumu, Nagai Yoshitaka

Abstract excerpt

We analyzed the clinical symptoms of hemiplegic migraine (HM) and their relevance in four Japanese patients considered to have ATP1A2 mutations as a cause. Sequencing of ATP1A2 was performed using the Sanger method in 43 blood samples from clinically suspected patients with familial HM. Subsequently, algorithm analysis, allele frequency determination, and three-dimensional structure analysis of the recognized...

Read the complete abstract on PubMed

Topics

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

Share to Hemiplegia
Share to Japan

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Migraine Disorders

Share to Migraine with Aura

Share to Mutation

Share to Mutation, Missense

Share to Sodium-Potassium-Exchanging ATPase

Source

Identifiers

PMID: 35257835
DOI: 10.1016/j.neures.2022.03.002

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

Hemiplegic migraine type 2 with new mutation of the ATP1A2 gene in Japanese cases.PMID 35257835Read ↗

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

A wide clinical phenotype spectrum in patients with ATP1A2 mutations.Semantic proximity Read ↗

Familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2.Semantic proximity Read ↗

ATP1A2 mutations in 11 families with familial hemiplegic migraine.Semantic proximity Read ↗

Familial basilar migraine associated with a new mutation in the ATP1A2 gene.Semantic proximity Read ↗

Comprehensive Exonic Sequencing of Hemiplegic Migraine-Related Genes in a Cohort of Suspected Probands Identifies Known and Potential Pathogenic Variants.Semantic proximity Read ↗

Clinical spectrum in three families with familial hemiplegic migraine type 2 including a novel mutation in the ATP1A2 gene.Semantic proximity Read ↗

[Sporadic hemiplegic migraine due to a missense variation in ATP1A2 gene in 2 children].Semantic proximity Read ↗

Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation.Semantic proximity Read ↗

Genetic effects of ATP1A2 in familial hemiplegic migraine type II and animal models.Semantic proximity Read ↗

Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2.Semantic proximity Read ↗

Expanding the Genetic and Clinical Spectrum of SCN1A-Related Hemiplegic Migraine: Analysis of Mutations in JapaneseSemantic proximity Read ↗

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