Familial Hemiplegic Migraine With Progressive Cerebellar Ataxia Caused by a p.Thr666Met CACNA1A Gene Mutation in a Chinese Family
Author:
Publisher
Frontiers Media SA
Subject
Neurology (clinical),Neurology
Reference22 articles.
1. Genetics of migraine;Anttila;Handb Clin Neurol.,2018
2. Sporadic and familial hemiplegic migraine: pathophysiological mechanisms, clinical characteristics, diagnosis, and management;Russell;Lancet Neurol.,2011
3. The International Classification of Headache Disorders, 3rd edition;Cephalalgia,2018
4. Advance in genetics of migraine;de Boer;Curr Opin Neurol.,2019
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1. Inactivation influences the extent of inhibition of voltage-gated Ca+2 channels by Gem—implications for channelopathies;Frontiers in Physiology;2023-08-16
2. Two pediatric patients with hemiplegic migraine presenting as acute encephalopathy: case reports and a literature review;Frontiers in Pediatrics;2023-07-28
3. Sporadic hemiplegic migraine with CACNA1A mutation masquerading as acute meningoencephalitis;Annals of Indian Academy of Neurology;2022
4. Diversity of CACNA1A-related disorders;Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova;2021
5. CACNA1A Gene Variants in Eight Chinese Patients With a Wide Range of Phenotypes;Frontiers in Pediatrics;2020-12-03
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