Familial “Diplegic” Migraine – Description of a Family With a Novel CACNA1A Mutation
Author:
Affiliation:
1. Department of Neurological Sciences The University of Vermont Burlington VT USA
2. Larner College of Medicine The University of Vermont Burlington VT USA
3. Department of Genetics University of Vermont Medical Center Burlington VT USA
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/head.13741
Reference28 articles.
1. The International Classification of Headache Disorders, 3rd edition (beta version)
2. Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4
3. Immunochemical identification and subcellular distribution of the alpha 1A subunits of brain calcium channels
4. Neurobiology of migraine
5. A Cacna1a Knockin Migraine Mouse Model with Increased Susceptibility to Cortical Spreading Depression
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1. Two pediatric patients with hemiplegic migraine presenting as acute encephalopathy: case reports and a literature review;Frontiers in Pediatrics;2023-07-28
2. Hemiplegic Migraine;Current Neurology and Neuroscience Reports;2023-05-29
3. Cerebro-Cerebellar Networks in Migraine Symptoms and Headache;Frontiers in Pain Research;2022-07-13
4. CACNA1A Gene Variants in Eight Chinese Patients With a Wide Range of Phenotypes;Frontiers in Pediatrics;2020-12-03
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