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Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
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Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
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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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Clinicopathological Study of 35 Cases of Multiple System Atrophy
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Trinucleotide Repeat Expansion in Neurological Disease
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Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
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Presynaptic Parkinsonism in Olivopontocerebellar Atrophy:Clinical, pathological, and Neurochemical Evidence
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Neuropsychological Changes in Olivopontocerebellar Atrophy
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A Quantitative Evaluation of Pontine Volume by Computed Tomography in Patients with Cerebral Degeneration
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Cerebellar & Brainstem Hypometabolism in Olivo-pontocerebellar Atrophy Detected with Positron Emission Tomography
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Spinocerebellar Degeneration:Qualitative & Quantitative MR Analysis of Atrophy
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Sleep Apnea in Olivopontocerebellar Degeneration:Treatment with Trazodone
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The Role of Glutamate in Neurotransmission & in Neurologic Disease
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Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
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Glutamate Dehydrogenase Deficiency in Patients with Olivopontocerebellar Atrophy
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Evoked Potentials in Olivopontocerebellar Atrophy
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Dominant Spinopontine Atrophy
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Dominant Spinopontine Atrophy
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Physostigmine in Familial Ataxias
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A Case of Cerebellar Ataxia, with a Discussion of Classification
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A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
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A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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Hypointensity of the Basal Ganglia in Adults with Glucose Transporter Protein Type 1 Deficiency Syndrome: A Novel Magnetic Resonance Imaging Finding
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Burning Pain in the Legs
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Clinicopathologic Conference, HIV Type 2 Infection & Cerebral Toxoplasmosis
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Neurosyphilis
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Progressive Gait Difficulty and Incontinence in a 40-year-old Man with HIV
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A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
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A 46-year-old man with Persistent Hiccups, Cognitive Dysfunction, and Imbalance
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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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