Acute Striatal Necrosis in Hemiplegic Migraine With de Novo CACNA1A Mutation
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1526-4610.2011.02014.x/fullpdf
Reference14 articles.
1. Familial hemiplegic migraine;Pietrobon;Neurother,2007
2. Defective membrane expression of the Na+-HCO3- cotransporter NBCe1 is associated with familial migraine;Suzuki;PNAS,2010
3. De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine;Riant;Neurology,2010
4. Prolonged hemiplegic episodes in children due to mutations in ATP1A2;Jen;J Neurol Neurosurg Psychiatry,2007
5. Prolonged sporadic hemiplegic migraine associated with a novel de novo missense ATP1A2 gene mutation;De Sanctis;Headache,2011
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1. Familial hemiplegic migraine;Handbook of Clinical Neurology;2024
2. Two pediatric patients with hemiplegic migraine presenting as acute encephalopathy: case reports and a literature review;Frontiers in Pediatrics;2023-07-28
3. The genotype–phenotype correlations of the CACNA1A-related neurodevelopmental disorders: a small case series and literature reviews;Frontiers in Molecular Neuroscience;2023-07-24
4. CACNA1A-Related Channelopathies: Clinical Manifestations and Treatment Options;Voltage-gated Ca2+ Channels: Pharmacology, Modulation and their Role in Human Disease;2023
5. Next-generation sequencing identified a novel CACNA1A I1379F variant in a familial hemiplegic migraine type 1 pedigree;Medicine;2021-12-23
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