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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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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, Friedreich Ataxia
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The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
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Fragile X Premutation With Atypical Symptoms at Onset
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The Parkinsonian Phenotype of Spinocerebellar Ataxia Type 2
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Clinical Features and ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10
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SCA-12: Tremor with Cerebellar and Cortical Atrophy is Associated with a CAG Repeat Expansion
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Spinocerebellar Ataxia Type 2 Presenting as Familial Levodopa-Responsive Parkinsonism
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Spinocerebellar Ataxia Type 8
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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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Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
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CAG Repeat Number Correlates with the Rate of Brainstem and Cerebellar Atrophy in Machado-Joseph Disease
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Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
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Isolated Vitamin E Deficiency
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