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Hereditary Form of Parkinsonism-Dementia
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Mendelian Etiologies of Stroke
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Multiple Sclerosis & Systemic Lupus Erythematosus, Occurrence in Two Generations of the Same Family
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A 63-Year-Old Female Patient Presenting with Orthostatic Hypotension and Ataxia
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Adult-Onset Coats Plus, A Case of Leukoencephalopathy with Calcifications, a Tumefactive Brain Lesion, and a Presumed Autoimmune Disease
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A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
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Amyotrophic Lateral Sclerosis
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Spinal Muscular Atrophy
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Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
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Duchenne Muscular Dystrophy
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A 22-Year-Old Man with Progressive Bilateral Visual Loss
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A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
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Ehlers-Danlos Syndromes
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Muscular Dystrophies
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Clinicopathologic Conference, Vascular Malformations in Liver, Stomach, Esophagus, and Lungs that are Consistent with Hereditary Hemorrhagic Telangiectasia, Complicated
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Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
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Neuroimaging Changes in Menkes Disease, Part 1
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A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
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Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use
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Non-Alzheimers Dementia 1 Frontotemporal Dementia
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Spinal Muscular Atrophy A Timely Review
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Genetics of Familial Amyotrophic Lateral Sclerosis
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Tuberous Sclerosis Complex: A Tale of Two Genes
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Tuberous Sclerosis
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Amyotrophic Lateral Sclerosis
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Parental Transmission of MS in a Population-Based Canadian Cohort
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Metabolic Disease and Stroke: MELAS
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The Tuberous Sclerosis Complex
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Adrenoleukodystrophy
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Familial Multiple Sclerosis and Other Inherited Disorders of the White Matter
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Clinical Profile of Stroke in 900 Patients with Hypertrophic Cardiomyopathy
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Amyotrophic Lateral Sclerosis
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National Institutes of Health Consensus Conference: Tuberous Sclerosis Complex
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Conjugal Multiple Sclerosis: Population-Based Prevalence and Recurrence Risks in Offspring
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De Novo Mutation in the Notch3 Gene Causing CADASIL
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Distal Hereditary Upper Limb Muscular Atrophy
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The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
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