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Showing articles 0 to 6 of 6 Filter Applied: cerebellar atrophy,primary (Click to remove) Chronic Neurodegenerative Disease Associated with HTLV-II Infection Lancet 339:645-646, Hjelle,B.,et al, 1992 Complex Ataxia Neurol 95:136-141, Abkur, T.,et al, 2020 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 Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria Neurol 52:1472-1478, Nardocci,N.,et al, 1999 Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum Neurol 39:1446-1452, Farlow,M.R.,et al, 1989 Showing articles 0 to 6 of 6