More Than a Little Unsteady
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Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
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Neuronal Intranuclear Inclusion Disease Cases with Leukoencephalopathy Diagnosed via Skin Biopsy
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Neurologic Manifestations of von Hippel-Lindau Disease
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Creutzfeldt-Jacob Disease in a Husband and Wife
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Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
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Fatal Insomnia in a Case of Familial Creutzfeldt-Jakob Disease with the Codon 200Lys Mutation
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Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
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Mutation of the Prion Protein in Libyan Jews with Creutzfeldt-Jakob Disease
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Familial Creutzfeldt-Jakob Disease without Periodic EEG Activity
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Supranuclear Gaze Palsy in Familial Creutzfeldt-Jakob Disease
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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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Hereditary Hemorrhagic Telangiectasia, Clinical Presentations, and Management
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Amyotrophic Lateral Sclerosis
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Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
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A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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Complex Ataxia
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Recurrent Cerebral Ischemia During Pregnancies
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Ehlers-Danlos Syndromes
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Recurrent Epistaxis in an Adolescent
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Cranial Cavernous Malformations
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Essential Tremor
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Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
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Clinicopathologic Conference, Vascular Malformations in Liver, Stomach, Esophagus, and Lungs that are Consistent with Hereditary Hemorrhagic Telangiectasia, Complicated
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A 13-year-old boy with Chronic Ataxia and Developmental Delay
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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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Neuromyelitis Optica Spectrum Disorders
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A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
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Red Papules on the Tongue of a Patient with Hemiparesis
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Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Gertsmann-Straussler Schneinker Syndrome
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Degenerative Diseases of the Nervous System, Parkinson Disease
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Degenerative Diseases of the Nervous System, Friedreich Ataxia
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Degenerative Diseases of the Nervous System, Cerebellar Degeneration
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Degenerative Diseases of the Nervous System, Olivopontocerebellar Atrophy
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Degenerative Diseases of the Nervous System, Machado-Joseph-Azorean Disease
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Degenerative Diseases of the Nervous System, Hereditary Spastic Paraplagia
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Brain Arteriovenous Malformation Multiplicity Predicts the Diagnosis of Hereditary Hemorrhagic Telangiectasia Quantitive Assessment
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Cerebral Amyloid Angiopathy
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CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis
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