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Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
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Neuroimaging Findings in Human Prion Disease
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Spinocerebellar Ataxia Type 10 is Rare in Populations Other Than Mexicans
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SCA-12: Tremor with Cerebellar and Cortical Atrophy is Associated with a CAG Repeat Expansion
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Trinucleotide Repeat Expansion in Neurological Disease
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Molecular Genetics in Neurology
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Mutation of the Prion Protein in Libyan Jews with Creutzfeldt-Jakob Disease
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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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Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
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NEJM 315:997-1003, Lugaresi,E.,et al, 1986
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Progressive Pontobulbar Palsy With Deafness
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Azorean Disease of the Nervous System
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Brugada Syndrome in Spinal and Bulbar Muscular Atrophy
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Spinal Muscular Atrophy A Timely Review
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Genetics of Familial Amyotrophic Lateral Sclerosis
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Glycogen-Storage Disease Type II
eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006
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