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Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
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Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
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Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
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Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
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Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
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A Family with Hereditary Ataxia:HLA Typing
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Clin. Path. Conference
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Dominant Spinopontine Atrophy
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Physostigmine in Familial Ataxias
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Spinocerebellar Ataxia & HLA Linkage:Risk Prediction by HLA Typing
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A 48-Year-Old Woman Presenting with Vertigo, Ptosis, and Red Eyes
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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Cogan Syndrome
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The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
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Clinicopath Conf., Paraneoplastic Cerebellar Degeneration Due to Anti-Yo Antibodies From Breast Cancer
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Congenital Lymphocytic Choriomeningitis Virus Infection: Spectrum of Disease
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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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Neuroradiologic Findings in Marinesco-Sjogren Syndrome
AJNR 19:281-283, Georgy,B.A.,et al, 1998
Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
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Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
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Neuroradiologic Aspects of Chester-Erdheim Disease
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Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
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Cogan's Syndrome:18 Cases & a Review of the Literature
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Ataxia with Aniridia of Gillespie:A Case Report
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Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
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Trichinosis with Central Nervous System Involvement
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