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A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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Choreoathetosis, Dystonia, and Myoclonus in 3 Siblings with Autosomal Recessive Spinocerebellar Ataxia Type 16
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A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
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Degenerative Diseases of the Nervous System, Multiple System Atrophy
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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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The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
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Chronic Pain in Machado-Joseph Disease: A Frequent and Disabling Symptom
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The Clinical and Genetic Spectrum of Spinocerebellar Ataxia 14
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Autonomic Dysfunction in Machado-Joseph Disease
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Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
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The Parkinsonian Phenotype of Spinocerebellar Ataxia Type 2
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Clinical Features and Neuropathology of Autosomal Dominant Spinocerebellar Ataxia (SCA17)
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Clinical Features and ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10
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Spinocerebellar Ataxia Type 10 is Rare in Populations Other Than Mexicans
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Spinocerebellar Ataxia Type 2 Presenting as Familial Levodopa-Responsive Parkinsonism
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Evolution of Sporadic Olivopontocerebellar Atrophy Into Multiple System Atrophy
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Cardiac Dysfunction in Neuromuscular Diseases
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Molecular Basis of the Neurodegenerative Disorders
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Clinical and MRI Findings in Spinocerebellar Ataxia Type 5
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CAG Repeat Number Correlates with the Rate of Brainstem and Cerebellar Atrophy in Machado-Joseph Disease
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Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
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Clinical Usefulness of Magnetic Resonance Imaging in Multiple System Atrophy
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Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
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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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Characteristic Magnetic Resonance Imaging Findings in Machado-Joseph Disease
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Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
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Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
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Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
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Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl
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Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
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Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
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Clinicopathological Study of 35 Cases of Multiple System Atrophy
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Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
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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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Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
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PET Studies on the Dopaminergic Sys & Striatal Opioid Binding in the OPCA Variant of Multiple System Atrophy
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Dopa-Responsive parkinsonism Phenotype of Machado-Jospeh Disease:Confirmation of 14q CAG Expansion
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Trinucleotide Repeat Expansion in Neurological Disease
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Molecular Genetics in Neurology
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Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Presynaptic Parkinsonism in Olivopontocerebellar Atrophy:Clinical, pathological, and Neurochemical Evidence
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Olivopontocerebellar Atrophy:MR Diagnosis and Relationahip to Multisystem Atrophy
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Neuropsychological Changes in Olivopontocerebellar Atrophy
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