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Progressive Pontobulbar Palsy With Deafness
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A 60-Year-Old Man with Weakness and Gait Dysfunction
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Distal Hereditary Upper Limb Muscular Atrophy
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Hereditary Form of Parkinsonism-Dementia
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Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
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Intrafamilial Heterogeneity in Hereditary Motor Neuron Disease
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Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
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Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
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The Molecular Genetic Revolution, Its Impact on Clinical Neurology
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Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
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Location of the Gene for X-Linked Spinal Muscular Atrophy
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Familial Occurrence of Amyotrophic Lateral Sclerosis, Parkinsonism, & Dementia
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Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
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Epidemiology of Motor-Neuron Diseases
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A 2-Year-Old Girl with Acute Encephalopathy After Febrile Systemic Illness
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Tuberous Sclerosis Complex: A Tale of Two Genes
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Adrenoleukodystrophy
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Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
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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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Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
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The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Mendelian Etiologies of Stroke
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Clinicopathological Conference
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Niemann-Pick Type C Disease
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A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
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Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
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The Spectrum of Fragile X Disorders
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A 9-Year-Old Girl with CNS Immune Dysregulation
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