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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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Adult Patient Presenting with Spine Pain Following a Motor Vehicle Accident
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A 53-year-old Woman with Lower Extremity Paresthesias
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Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
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A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
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A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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Non-Alzheimers Dementia 1 Frontotemporal Dementia
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Chronic and Slowly Progressive Weakness of the Legs and Hands
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Brugada Syndrome in Spinal and Bulbar Muscular Atrophy
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A 52-year-old Woman with Progressive Proximal Weakness
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Degenerative Diseases of the Nervous System, Kennedy Syndrome (X-Linked Bulbospinal Muscular Atrophy)
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
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Amyotrophic Lateral Sclerosis
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Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
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Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
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Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Comparison of First Degree Relatives and Spouses of Poeple with Chronic Tension Headache
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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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Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
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Benign Familial Disease with Muscle Mounding and Rippling
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Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
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Neurologic Crises in Hereditary Tyrosinemia
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Acute Intermittent Porphyria
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Cylindrical Spirals in a Familial Neuromuscular Disorder
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Familial Psychosis & Diverse Neurologic Abnormalities in Adult-Onset Gaucher's Disease
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Hereditary Quadriceps Myopathy
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A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
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Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
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A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
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Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
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Clinodactyly as a Key Finding in Distal Spinal Muscular Atrophy
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AAV9-Mediated Gene Therapy for Infantile-Onset Pompes Disease
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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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Multivessel Cerebral Occlusion in Noonan Syndrome
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Melas Syndrome
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
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A 24-Year-Old Man with Spastic Ataxia and Hypodontia
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