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A 23-Year-Old Man With Seizures and Visual Deficit
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De Novo Mutation in the Notch3 Gene Causing CADASIL
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Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus
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Mitochondrial DNA and Disease
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Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
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Clinical Spectrum of CADASIL:A Study of 7 Families
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New Phenotype of the Cerebral Autosomal Dominant Arteriopathy Mapped to Chromosome 19:Migraine as the Prominent Clinical Feature
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Progress in the Genetics of Cerebrovascular Disease Inherited Subcortical Arteriopathies
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MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission
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