Spinocerebellar ataxia type 6 and episodic ataxia type 2: differences and similarities between two allelic disordersMANTUANO, E; VENEZIANO, L; JODICE, C et al.Cytogenetic and genome research. 2003, Vol 100, Num 1-4, pp 147-153, issn 1424-8581, 7 p.Article

Profile of families with Parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2)FURTADO, Sarah; PAYAMI, Haydeh; DE LA FUENTE-FERNANDEZ, Raul et al.Movement disorders. 2004, Vol 19, Num 6, pp 622-629, issn 0885-3185, 8 p.Article

Spinocerebellar ataxia type 5: Clinical and molecular genetic features of a German kindredBÜRK, K; ZÜHLKE, C; KÖNIG, I. R et al.Neurology. 2004, Vol 62, Num 2, pp 327-329, issn 0028-3878, 3 p.Article

The parkinsonian phenotype of spinocerebellar ataxia type 2LU, Chin-Song; CHOU, Yah-Huei Wu; KUO, Pei-Chi et al.Archives of neurology (Chicago). 2004, Vol 61, Num 1, pp 35-38, issn 0003-9942, 4 p.Article

Molecular genetics of hereditary spinocerebellar ataxia: Mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian familiesBRUSCO, Alfredo; GELLERA, Cinzia; TARONI, Franco et al.Archives of neurology (Chicago). 2004, Vol 61, Num 5, pp 727-733, issn 0003-9942, 7 p.Article

Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10MATSUURA, Tohru; PING FANG; ZOGHBI, Huda Y et al.American journal of human genetics. 2004, Vol 74, Num 6, pp 1216-1224, issn 0002-9297, 9 p.Article

A novel haplotype of spinocerebellar ataxia type 6 contributes to the highest prevalence in Western JapanTERASAWA, Hideo; ODA, Masaya; MORINO, Hiroyuki et al.Neuroscience letters. 2004, Vol 358, Num 2, pp 107-110, issn 0304-3940, 4 p.Article

Peripheral nerve involvement in spinocerebellar ataxiasVAN DE WARRENBURG, Bart P. C; NOTERMANS, Nicolette C; SCHELHAAS, Helenius J et al.Archives of neurology (Chicago). 2004, Vol 61, Num 2, pp 257-261, issn 0003-9942, 5 p.Article

Spinocerebellar ataxia type 8: Molecular genetic comparisons and haplotype analysis of 37 families with ataxiaIKEDA, Yoshio; DALTON, Joline C; SHOJI, Mikio et al.American journal of human genetics. 2004, Vol 75, Num 1, pp 3-16, issn 0002-9297, 14 p.Article

Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2pSTEVANIN, Giovanni; BOUSLAM, Naima; THOBOIS, Stéphane et al.Annals of neurology. 2004, Vol 55, Num 1, pp 97-104, issn 0364-5134, 8 p.Article

Complex phenotypes in an Indian family with homozygous SCA2 mutationsRAGOTHAMAN, Mona; SARANGMATH, Nagaraja; THELMA, B. K et al.Annals of neurology. 2004, Vol 55, Num 1, pp 130-133, issn 0364-5134, 4 p.Article

Discoveries in sphingolipid metabolism, spinocerebellar ataxia and autoimmune diseaseBRUNHAM, Liam R; CHAN, Edmond Y. W; ORBAN, Paul C et al.Clinical genetics. 2003, Vol 64, Num 1, pp 1-6, issn 0009-9163, 6 p.Article

Electrophysiologic characterization in spinocerebellar ataxia 17MANGANELLI, F; PERRETTI, A; NOLANO, M et al.Neurology. 2006, Vol 66, Num 6, pp 932-934, issn 0028-3878, 3 p.Article

Saccade velocity is controlled by polyglutamine size in spinocerebellar ataxia 2VELAZQUEZ-PEREZ, Luis; SEIFRIED, Carola; VELAZQUEZ-MANRESA, Mercedes et al.Annals of neurology. 2004, Vol 56, Num 3, pp 444-447, issn 0364-5134, 4 p.Article

Expanded ATXN2 CAG repeat size in ALS identifies genetic overlap between ALS and SCA2VAN DAMME, P; VELDINK, J. H; VAN BLITTERSWIJK, M et al.Neurology. 2011, Vol 76, Num 24, pp 2066-2072, issn 0028-3878, 7 p.Article

The wide clinical spectrum and nigrostriatal dopaminergic damage in spinocerebellar ataxia type 6KIM, Jong-Min; LEE, Jee-Young; HEE JIN KIM et al.Journal of neurology, neurosurgery and psychiatry. 2010, Vol 81, Num 5, pp 529-532, issn 0022-3050, 4 p.Article

Abraham Lincoln did not have type 5 spinocerebellar ataxiaSOTOS, John G.Neurology. 2009, Vol 73, Num 16, pp 1328-1332, issn 0028-3878, 5 p.Article

Spinocerebellar ataxia type 20 is genetically distinct from spinocerebellar ataxia type 5LORENZO, D. N; FORREST, S. M; IKEDA, Y et al.Neurology. 2006, Vol 67, Num 11, pp 2084-2085, issn 0028-3878, 2 p.Article

The clinical and genetic spectrum of spinocerebellar ataxia 14CHEN, D.-H; CIMINO, P. J; WOLFF, J et al.Neurology. 2005, Vol 64, Num 7, pp 1258-1260, issn 0028-3878, 3 p.Article

Spinocerebellar ataxia type 2 with glial cell cytoplasmic inclusionsPROBST-COUSIN, S; ACKER, T; EPPLEN, J. T et al.Journal of neurology, neurosurgery and psychiatry. 2004, Vol 75, Num 3, pp 503-505, issn 0022-3050, 3 p.Article

Spinocerebellar ataxia type 8 in Scotland: genetic and c inical features in seven unrelated cases and a review of published reportsZEMAN, A; STONE, J; PORTEOUS, M et al.Journal of neurology, neurosurgery and psychiatry. 2004, Vol 75, Num 3, pp 459-465, issn 0022-3050, 7 p.Article

Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C γYABE, Ichiro; SASAKI, Hidenao; CHEN, Dong-Hui et al.Archives of neurology (Chicago). 2003, Vol 60, Num 12, pp 1749-1751, issn 0003-9942, 3 p.Article

Les ataxies spinocérébelleuses = Spinocerebellar ataxiasTHAUVIN-ROBINET, C; FAIVRE, L; CAZENEUVE, C et al.La Lettre du neurologue. 2013, Num 8, pp 234-239, issn 1276-9339, 6 p.Article

Spinocerebellar ataxia types 1, 2, 3, and 6 : Disease severity and nonataxia symptomsSCHMITZ-HÜBSCH, T; COUDERT, M; RIBAI, P et al.Neurology. 2008, Vol 71, Num 13, pp 982-989, issn 0028-3878, 8 p.Article

Quantitative assessment of cerebral blood flow in genetically confirmed spinocerebellar ataxia type 6HONJO, Kie; OHSHITA, Tomohiko; KAWAKAMI, Hideshi et al.Archives of neurology (Chicago). 2004, Vol 61, Num 6, pp 933-937, issn 0003-9942, 5 p.Article