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Last Updated : 05/19/2022

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Found 15 publications

Next-generation sequencing identified a novel CACNA1A I1379F variant in a familial hemiplegic migraine type 1 pedigree: A case report.

Familial hemiplegic migraine.

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

CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family report.

A case report of atypical hemiplegic migraine with nonheadache onset in a Chinese child.

Bilateral persistent ophthalmoplegia in a patient with migraine: persistent migraine aura without infarction?

Clinical and genetic analysis of 5 pediatric patients with hemiplegic migraine presenting as acute encephalopathy.

Familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2.

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

Insights into pathophysiology and treatment of visual snow syndrome: A systematic review.

Manual acupuncture versus sham acupuncture and usual care for prophylaxis of episodic migraine without aura: multicentre, randomised clinical trial.

Familial hemiplegic migraine with a PRRT2 mutation: Phenotypic variations and carbamazepine efficacy.

Showing 1-12 of 15

Last Updated : 05/19/2022