Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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Degenerative Diseases of the Nervous System, Kennedy Syndrome (X-Linked Bulbospinal Muscular Atrophy)
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Oculopharyngeal Muscular Dystrophy in Hispanic New Mexicans
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Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
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Progressive Supranuclear Palsy-Case Study
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A 42-year-old Woman with Progressive Cognitive Difficulties and Gait Imbalance
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An 81-year-old Woman with Decreased Consciousness and Fluctuating Right Facial Droop
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Ears of the Lynx Magnetic Resonance Imaging Sign
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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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Clinicopathologic Conference, Amyotrophic Lateral Sclerosis
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Strokelike Episodes in a Patient with Chronic Gait Abnormalities
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A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
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Man with Recurrent Paralysis and Cerebral White Matter Lesions
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
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Motor Neurone Disease
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The Acquired Metabolic Disorders of the Nervous System, Cretinism and Neonatal Myxedema
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Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis
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Degenerative Diseases of the Nervous System, Progressive Bulbar Palsy
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Clinical Reasoning: A Young Man with Reversible Paralysis, Cerebral White Matter Lesions, and Peripheral Neuropathy
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A 23-Year-Old Man With Seizures and Visual Deficit
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Diagnosis and Management of Motor Neurone Disease
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JC Viral Infection-Related Cerebellar Degeneration as the First Manifestation of AIDS
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Amyotrophic Lateral Sclerosis
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Spinocerebellar Ataxia Type 8
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Cerebellar Degeneration Associated With Human Immunodeficiency Virus Infection
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Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
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Speech Motor Control Disorder after HIV Infection
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Congenital Bilateral Perisylvian Syndrome:Study of 31 Patients
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Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Progressive Rubella Panencephalitis
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Misdiagnosis in Patients with Amyotrophic Lateral Sclerosis
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Clinical Features and Associations of 560 Cases of Motor Neuron Disease
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Dominant Spinopontine Atrophy
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Azorean Disease of the Nervous System
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