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

Pediatric sporadic hemiplegic migraine (ATP1A2 gene): a case report and brief literature review.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology - 1 Jun 2018

Schwarz Ghil, Anzalone Nicoletta, Baldoli Cristina, Impellizzeri Matteo, Minicucci Fabio, Comi Giancarlo, Colombo Bruno

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 Adolescent
Share to Electroencephalography
Share to Functional Laterality

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Magnetic Resonance Imaging

Share to Migraine Disorders

Share to Mutation

Share to Sodium-Potassium-Exchanging ATPase

Source

Identifiers

PMID: 29904856
DOI: 10.1007/s10072-018-3405-3

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

Pediatric sporadic hemiplegic migraine (ATP1A2 gene): a case report and brief literature review.PMID 29904856Read ↗

[Familial hemiplegic migraine type 2: two paediatric case reports].Semantic proximity Read ↗

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

Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation.Semantic proximity Read ↗

Familial hemiplegic migraine in pediatric patients: A genetic, clinical, and follow-up study.Semantic proximity Read ↗

Alternating Hemiplegia of Childhood Caused by ATP1A3 Mutations: A Report of Two Cases.Semantic proximity Read ↗

Sporadic hemiplegic migraine.Semantic proximity Read ↗

The clinical spectrum associated with ATP1A2 variants in Chinese pediatric patients.Semantic proximity Read ↗

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

An Infant With Epilepsy and Recurrent Hemiplegia due to Compound Heterozygous Variants in ATP1A2.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 ↗

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

De novo exonic duplication of ATP1A2 in Italian patient with hemiplegic migraine: a case report.Semantic proximity Read ↗

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