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Metabolic Disease and Stroke: MELAS
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Cerebrovascular Complications of Fabry's Disease
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Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus
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Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
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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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Ornithine Transcarbamylase Deficiency Presenting with Strokelike Episodes
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A Familial Disorder with Subcortical Ischemic Strokes, Dementia, and Leukoencephalopathy
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Hematologic Disorders and Ischemic Stroke
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Livedo Reticularis, Porcelain-White Scars, and Cerebral Thromboses
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A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
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A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
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RNF213 Polymorphisms in Intracranial Artery Dissection
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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Neonatal Seizures
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Pediatric Leigh Syndrome
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Clinical Reasoning: A Teenager with Left Arm Weakness
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Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
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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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Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
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A Case of Refractory Nocturnal Seizures
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Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use
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Molybdenum Cofactor Deficiency
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Sturge-Weber Syndrome
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Brain Arteriovenous Malformation Multiplicity Predicts the Diagnosis of Hereditary Hemorrhagic Telangiectasia Quantitive Assessment
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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
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Genomewide Association Studies of Stroke
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The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
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Decoding Cryptogenic Cardioembolism
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Pulmonary Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia: A Series of 126 Patients
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Parental Transmission of MS in a Population-Based Canadian Cohort
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Prevalence of Fabry Disease in Patients with Cryptogenic Stroke: A Prospective Study
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Epilepsy Syndromes in Infancy
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