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The Motor Disorder of Multiple System Atrophy
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Neurologic Sequelae of Chronic Solvent Vapor Abuse
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Long-Term Treatment of Cerebrotendinous Xanthomatosis with Chenodeoxycholic Acid
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SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
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CMT with Pyramidal Features
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Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
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Asymmetrical Skin Temperature in Ischemic Stroke
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Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
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Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
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Neurologic Aspects of Cobalamin Deficiency
Medicine 70:229-245, Healton,E.B.,et al, 1991
Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Familial Idiopathic Striopallidodentate Calcifications
Neurol 39:381-385, Ellie,E.,et al, 1989
Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
Neurol 39:1446-1452, Farlow,M.R.,et al, 1989
Pyramidal Tract Deficits & Polyneuropathy in Hyperthyroidism
Am J Med 78:1041-1044, Fisher,M.,et al, 1985
Multifocal Central Nervous System Damage Caused by Toluene Abuse
Neurol 33:1337-1340, Lazar,R.B.,et al, 1983
Clinical Criteria for Diagnosis of Machado-Joseph Disease:Report of a Non-Azorean Portuguese Family
Neurol 30:319-322, Lima,L.,et al, 1980
Chronic Meningitis
Medicine 55:341, Ellner,J.J.,et al, 1976
Mollaret's Meningitis & Differential Diagnosis of Recurrent Meningitis
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Brain Stem Tumors of Childhood & Adolescence
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