Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
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A 23-Year-Old Man With Seizures and Visual Deficit
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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Ataxia, Dementia, and Hypogonadotropism Caused by Disordered Ubiquitination
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Auto-Immune Cerebellar Ataxia with Anti-GAD Antibodies Accompanied by De Novo Late-Onset Type 1 Diabetes Mellitus
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Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
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Cerebellar Ataxia With Anti-Glutamic Acid Decarboxylase Antibodies
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SCA-12: Tremor with Cerebellar and Cortical Atrophy is Associated with a CAG Repeat Expansion
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Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
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Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
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Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
BMJ 315:856-857, Fox,N.C.,et al, 1997
Autoantibodies to Glutamic Acid Decarboxylase in Three Patients With Cerebellar Ataxia, Late-Onset Insulin-Dependent Diabetes Mellitus, and Polyendocrine Autoimmunity
Neurol 49:1026-1030, Saiz,A.,et al, 1997
Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
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Chronic Neurodegenerative Disease Associated with HTLV-II Infection
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Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
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The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
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Magnetic Resonance Imaging in Familial Paroxysmal Ataxia
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