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Jaw Drop in Kennedy's Disease
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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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Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
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X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome) A Kindred with Hypobetalipoproteinemia
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Amyotrophic Lateral Sclerosis
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Ears of the Lynx Magnetic Resonance Imaging Sign
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A 42-year-old man with unilateral leg weakness
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A Neonate with Micrognathia and Hypotonia
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Degenerative Diseases of the Nervous System, Kugelberg-Welander Syndrome SMAIII
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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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Spinal Muscular Atrophy
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Familial Amyotrophic Lateral Sclerosis
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Amyotrophic Lateral Sclerosis
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Clinical and Genetic Aspects of Distal Myopathies
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Congenital Muscular Dystrophy with Rigid Spine Syndrome:A Clinical, Pathological, Radiological, and Genetic Study
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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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Familial Nature and Continuing Morbidity of the Amyotrophic Lateral Sclerosis-Parkinsonism Dementia Complex of Guam
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Superoxide Dismutase and ALS
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Monomelic Amyotrophy
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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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Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
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Familial Adult-Onset Muscular Dystrophy with Leukoencephalopathy
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Welander's Distal Myopathy:Clinical Neurophysiol & Muscle Biopsy Obser in Young & Middle Aged Adults with Early Symptoms
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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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Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
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Familial Adult Motor Neuron Disease:Amyotrophic Lateral Sclerosis
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The Oculopharyngeal Syndrome
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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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A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
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Leber Hereditary Optic Neuropathy with Longitudinal Spinal Cord Lesion Mimicking Spinal Cord Infarction
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A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
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A 53-year-old Woman with Lower Extremity Paresthesias
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Complex Ataxia
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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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A 54-year-old man with Dyspnea and Muscle Weakness
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Strokelike Episodes in a Patient with Chronic Gait Abnormalities
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Clinicopathologic Conference, Lebers Hereditary Optic Neuropathy
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A 60-year-old man with arm weakness and numbness
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