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Nature Genetics|November 1, 1993
Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type IM Y Chung, L P Ranum, L A Duvick, et al.Human Molecular Genetics|January 1, 1996
Cloning and developmental expression analysis of the murine homolog of the spinocerebellar ataxia type 1 gene (Sca1)S Banfi, A Servadio, M Chung, et al.Functional Neurology|June 8, 2019
Evaluation of the psychometric properties of the Barthel Index in an Italian ischemic stroke population in the acute phase: a cross-sectional studyG Galeoto, M C Formica, N B Mercuri, et al.Nature|November 14, 1997
Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structuresP J Skinner, B T Koshy, C J Cummings, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 5, 2003
Dementia, ataxia, extrapyramidal features, and epilepsy: phenotype spectrum in two Italian families with spinocerebellar ataxia type 17G De Michele, F Maltecca, M Carella, et al.Neurology|November 26, 2003
Intergenerational instability and marked anticipation in SCA-17F Maltecca, A Filla, I Castaldo, et al.Cell|September 22, 1995
SCA1 transgenic mice: a model for neurodegeneration caused by an expanded CAG trinucleotide repeatE N Burright, H B Clark, A Servadio, et al.Cytopathology : Official Journal of the British Society for Clinical Cytology|November 21, 2013
Histo-cytological diagnostic accuracy in lung cancerA Proietti, L Boldrini, G Alì, et al.Nature Genetics|August 1, 1994
Identification and characterization of the gene causing type 1 spinocerebellar ataxiaS Banfi, A Servadio, M Y Chung, et al.Nature Genetics|July 1, 1993
Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1H T Orr, M Y Chung, S Banfi, et al.Pageof 2