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• W2149380069 abstract "We report the case of a 9-year-old girl with early-onset developmental delay, chronic ataxia and prolonged hemiplegic migraine episodes bringing about progressive deterioration. Two days into one episode, diffusion-weighted magnetic resonance imaging disclosed unilateral striatal abnormal signal consistent with cytotoxic edema, which evolved into atrophy on follow-up scans. Mutational screen of CACNA1A gene identified a de novo p.Tyr1387Cys mutation." @default.
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• W2149380069 date "2011-11-01" @default.
• W2149380069 modified "2023-10-06" @default.
• W2149380069 title "Acute Striatal Necrosis in Hemiplegic Migraine With de Novo CACNA1A Mutation" @default.
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• W2149380069 doi "https://doi.org/10.1111/j.1526-4610.2011.02014.x" @default.
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