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 with reversible cerebral vasoconstriction caused by ATP1A2 mutations.

Journal of neurology - 1 Aug 2013

Hermann Andreas, Engelandt Kay, Rautenstrauss Bernd, Reichmann Heinz, Jacobasch Eleonore

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 Cerebral Angiography
Share to Cerebrovascular Circulation
Share to Diffusion Magnetic Resonance Imaging
Share to Magnetic Resonance Angiography

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Migraine with Aura

Share to Migraine without Aura

Share to Sodium-Potassium-Exchanging ATPase

Share to Vasoconstriction

Source

Identifiers

PMID: 23821026
DOI: 10.1007/s00415-013-7010-3

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

Hemiplegic migraine with reversible cerebral vasoconstriction caused by ATP1A2 mutations.PMID 23821026Read ↗

Prolonged Hyperperfusion in a Child With ATP1A2 Defect-Related Hemiplegic Migraine.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 ↗

Diagnostic and therapeutic aspects of hemiplegic migraine.Semantic proximity Read ↗

Dissociated neurovascular dynamics in ATP1A2-related familial hemiplegic migraine mimicking acute ischemic stroke.Semantic proximity Read ↗

Familial hemiplegic migraine type 2 does not share hypersensitivity to nitric oxide with common types of migraine.Semantic proximity Read ↗

Neurovascular changes in prolonged migraine aura in FHM with a novel ATP1A2 gene mutation.Semantic proximity Read ↗

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

A novel ATP1A2 mutation in a family with FHM type II.Semantic proximity Read ↗

Early Treatment in Acute Severe Encephalopathy Caused by ATP1A2 Mutation of Familial Hemiplegic Migraine Type 2: Case Report and Literature Review.Semantic proximity Read ↗

Adult-onset Leigh Syndrome with a m.9176T>C Mutation Manifested As Reversible Cerebral Vasoconstriction Syndrome.Semantic proximity Read ↗

Intellectual Decline in a Patient with Migraine and APT1A2 Mutation: A Case ReportSemantic proximity Read ↗

Functional correlation of ATP1A2 mutations with phenotypic spectrum: from pure hemiplegic migraine to its variant forms.Semantic proximity Read ↗

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