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A 42-year-old man with unilateral leg weakness
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Spinal Muscular Atrophy
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Familial Amyotrophic Lateral Sclerosis
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Amyotrophic Lateral Sclerosis
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Distal Hereditary Upper Limb Muscular Atrophy
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Frontotemporal Dementia is on the MAP
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Prognosis in Familial ALS:Progr & Surv in Pts with glu100gly & ala4val Mutations in Cu, Zn Superoxide Dismutase
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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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Superoxide Dismutase and ALS
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Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
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Parental Sex Effect in Familial Amyotrophic Lateral Sclerosis
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Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
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Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
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Familial Adult Motor Neuron Disease:Amyotrophic Lateral Sclerosis
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A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
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Inherited Metabolic Diseases of the Nervous System, Hepatolenticular Degeneration (Wilson Disease)
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Degenerative Diseases of the Nervous System, Parkinson Disease
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MRI and EEG as long-term seizure outcome predictors in familial mesial temporal lobe epilepsy
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Migraine and Cerebral White Matter Lesions
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Alzheimer's Disease and Parkinson's Disease
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Familial Dementia With Lewy Bodies
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De Novo Mutation in the Notch3 Gene Causing CADASIL
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Familial Idiopathic Brain Calcification with Autosomal Dominant Inheritance
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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A 51-Year-Old Woman with Abnormal Corups Callosum Signal
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Vascular Malformations of the Central Nervous System
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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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Leber Hereditary Optic Neuropathy with Longitudinal Spinal Cord Lesion Mimicking Spinal Cord Infarction
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More Than a Little Unsteady
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Ears of the Lynx Magnetic Resonance Imaging Sign
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Clinicopathologic Conference,Aceruloplasminemia, Hereditary
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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
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GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
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