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Showing articles 0 to 4 of 4 Filter Applied: cerebellar atrophy,primary (Click to remove) Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia Neurol 104:e210253, Chadha,D.,et al, 2024 Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019 SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases Eur J Hum Genet 24:1016-1021, Choquet,K.,et al, 2016 The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990 Showing articles 0 to 4 of 4