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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Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
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A 53-year-old Woman with Lower Extremity Paresthesias
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A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
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A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
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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, Werdnig-Hoffman Disease, Spinal Muscular Atrophy
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The Autosomal Recessive Cerebellar Ataxias
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Clinical Reasoning: A Young Man with Reversible Paralysis, Cerebral White Matter Lesions, and Peripheral Neuropathy
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Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
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Distal Myopathies:Clinical and Molecular Diagnosis and Classification
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Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
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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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Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
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Cortically Evoked Motor Responses in Patients with Xp22. 3-Linked Kallmann's Syndrome and in Female Gene Carriers
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Brief Report:Intragenic Deletion of the Kalig-1 Gene in Kallmann's Syndrome
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Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Autosomal Dominant Cramping Disease
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Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
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Peripheral Neuropathy in Amyotrophic Chorea-Acanthocytosis
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Neurofibromatosis 2 (Bilateral Acoustic Neuro-fibromatosis)
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McArdle's Disease:Biochemical and Molecular Genetic Studies
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Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
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Familial Recurrent Bell's Palsy with Ocular Motor Palsies
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Cervicomedullary Compression in Young Patients with Achondroplasia:Value of Neurologic & Respiratory Eval
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Sclerosteosis:Neurogenetic & Pathophysiologic Analysis of an American Kinship
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Phytanic Acid Storage Disease:Hearing Maintained After 15 Years of Dietary Treatment
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Chronic Progressive External Ophthalmoplegia (CPEO) :Clinical, Morphologic, & Biochemical Studies
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Evoked Response Studies in Patients with Adreno-leukodystrophy & Heterozygous Relatives
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Detection Of Adrenoleucodystrophy Carriers By Means Of Evoked Potentials
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Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
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Juvenile Metachromatic Leukodystrophy
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Leber's Optic Neuropathy
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Quadriceps Myopathy in Two Brothers
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Obstructive Sleep Apnea in Family Members
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Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
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Familial Spasmodic Torticollis
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