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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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Amyotrophic Lateral Sclerosis
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MR Neurography for the Diagnosis of Hypertrophic Neuropathies
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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A 52-year-old Woman with Progressive Proximal Weakness
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Degenerative Diseases of the Nervous System, Parkinson Disease
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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The Occurence of Guillain-Barre Syndrome Within Families
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Cardiac Dysfunction in Neuromuscular Diseases
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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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Hereditary Spastic Paraplegia:Advances in Genetic Research
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Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
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Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
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Inclusion Body Myositis and Myopathies
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Anticonvulsant Hypersensitivity Syndrome
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Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
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Benign Familial Disease with Muscle Mounding and Rippling
JNNP 57:344-347, Burns,R.J.,et al, 1994
Familial Inclusion Body Myositis:Evidence for Autosomal Dominant Inheritance
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Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
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Delayed Diagnosis of Juvenile Myoclonic Epilepsy
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A Clinical Study of Noonan Syndrome
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Diagnostic Tests for Choreoacanthocytosis
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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Thyrotoxic Periodic Paralysis
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More Than a Little Unsteady
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A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
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