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A 60-Year-Old Man with Weakness and Gait Dysfunction
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A 59-Year-Old Female Patient with Urinary Dysfunction and Lightheadedness
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Spinal Muscular Atrophy
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Duchenne Muscular Dystrophy
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Ears of the Lynx Magnetic Resonance Imaging Sign
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Molybdenum Cofactor Deficiency
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Brugada Syndrome in Spinal and Bulbar Muscular Atrophy
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Degenerative Diseases of the Nervous System, Werdnig-Hoffman Disease, Spinal Muscular Atrophy
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Degenerative Diseases of the Nervous System, Kugelberg-Welander Syndrome SMAIII
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Psychosis in an Adolescent Girl: A Common Manifestation in Niemann-Pick Type C Disease
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Spinal Muscular Atrophy A Timely Review
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The Floppy Infant: Evaluation of Hypotonia
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Aicardi-Gouti�res Syndrome
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Genetics of Familial Amyotrophic Lateral Sclerosis
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Angelman Syndrome Revisited
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Glycogen-Storage Disease Type II
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Recessive Ataxia With Ocular Apraxia
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Amyotrophic Lateral Sclerosis
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Distal Hereditary Upper Limb Muscular Atrophy
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From Enigmatic to Problematic:The New Molecular Genetics of Childhood Spinal Muscular Atrophy
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Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
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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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Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
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DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
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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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