"Disappearing Infarct" Is Late-Onset MELAS
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Metabolic Disease and Stroke: MELAS
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Clinicopathological Conference
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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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Unilateral Leukoencephalopathy Revealing Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
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More Than a Little Unsteady
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Imaging Patterns Characterizing Mitochondrial Leukodystrophies
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Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
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Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
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A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
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A Young Man with Progressive Vision and Hearing Loss
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Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
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Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use
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Characyeristic features and progression of abnormalities on MRI for CARASIL
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Cerebral Abnormalities in Adults with Ataxia-Telangiectasia
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Sturge-Weber Syndrome
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Clinical Reasoning: A Young Man with Reversible Paralysis, Cerebral White Matter Lesions, and Peripheral Neuropathy
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Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
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Pulmonary Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia: A Series of 126 Patients
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Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
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Multiple Sclerosis
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De Novo Mutation in the Notch3 Gene Causing CADASIL
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Unusual Clinical Features and Early Brain MRI Lesions in a Family with Cerebral Autosomal Dominant Arteriopathy
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Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
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Stroke in Williams Syndrome
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Cerebrovascular Complications of Fabry's Disease
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Familial Cerebral Cavernous Angiomas:Clinical and Radiologic Studies
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Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus
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Ischemic Stroke in Young Pts with Activated Protein C Resistance:Rpt of Three Cases Belonging to Three Different Kindreds
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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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Neurovascular Manifestations of Heritable Connective Tissue Disorders:A Review
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Progress in the Genetics of Cerebrovascular Disease Inherited Subcortical Arteriopathies
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Ornithine Transcarbamylase Deficiency Presenting with Strokelike Episodes
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Intracranial Hemorrhage in Patients with Polycystic Kidney Disease
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