Cerebellar Ataxia With Anti-Glutamic Acid Decarboxylase Antibodies
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Degenerative Diseases of the Nervous System, Multiple System Atrophy
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Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
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The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
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Idiopathic Cerebellar Ataxia of Late Onset:Natural History and MRI Morphology
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