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Showing articles 0 to 7 of 7 Filter Applied: cerebellar atrophy,primary (Click to remove) 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 A 23-Year-Old Man With Seizures and Visual Deficit Neurol 70:73-78, Boustany,R.-M.,et al, 2008 Chronic Neurodegenerative Disease Associated with HTLV-II Infection Lancet 339:645-646, Hjelle,B.,et al, 1992 Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging Neurol 42:1220-1224, 1992,, Rando,T.A.,et al, 1992 Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum Neurol 39:1446-1452, Farlow,M.R.,et al, 1989 Showing articles 0 to 7 of 7