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

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

A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome lp21-q23CHUNG, Ming-Yi; LU, Yi-Chun; CHENG, Nai-Chia et al.Brain. 2003, Vol 126, pp 1293-1299, issn 0006-8950, 7 p., 6Article

Spinocerebellar ataxia type 6 (SCA6): neurodegeneration goes beyond the known brain predilection sitesGIERGA, K; SCHELHAAS, H. J; DELLER, T et al.Neuropathology and applied neurobiology (Print). 2009, Vol 35, Num 5, pp 515-527, issn 0305-1846, 13 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

Regional patterns of cerebral glucose metabolism in spinocerebellar ataxia type 2, 3 and 6 : A voxel-based FDG-positron emission tomography analysisWANG, Po-Shan; LIU, Ren-Shyan; YANG, Bang-Hung et al.Journal of neurology. 2007, Vol 254, Num 7, pp 838-845, issn 0340-5354, 8 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

Spinocerebellar ataxia type 2 : polyQ repeat variation in the CACNAIA calcium channel modifies age of onsetPULST, Stefan-M; SANTOS, Nieves; DAI WANG et al.Brain. 2005, Vol 128, pp 2297-2303, issn 0006-8950, 7 p., 10Article

Excessive daytime somnolence in spinocerebellar ataxia type 1DIEN DANG; CUNNINGTON, David.Journal of the neurological sciences. 2010, Vol 290, Num 1-2, pp 146-147, issn 0022-510X, 2 p.Article

Molecular analysis of spinocerebellar ataxia trinucleotide repeat behavior in normal individuals of a Brazilian populationWOLFGRAMM, Eldamaria De Vargas; MAGRI DE CARVALHO, Fernanda; PENHA DE NADAI SARTORI, Mariana et al.Journal of the neurological sciences. 2008, Vol 269, Num 1-2, pp 113-117, issn 0022-510X, 5 p.Article

Spinocerebellar ataxia type 2 (SCA2) with white matter involvementARMSTRONG, J; BONAVENTURA, I; ROJO, A et al.Neuroscience letters. 2005, Vol 381, Num 3, pp 247-251, issn 0304-3940, 5 p.Article

Proteolytic cleavage and cellular toxicity of the human α1A calcium channel in spinocerebellar ataxia type 6KUBODERA, Takayuki; YOKOTA, Takanori; OHWADA, Kiyoshi et al.Neuroscience letters. 2003, Vol 341, Num 1, pp 74-78, issn 0304-3940, 5 p.Article

Spinocerebellar ataxias types 1, 2 and 3 : Age adjusted clinical severity of disease at presentation correlates with size of CAG repeat lengthsNETRAVATHI, M; PRAMOD KUMAR PAL; PURUSHOTTAM, Meera et al.Journal of the neurological sciences. 2009, Vol 277, Num 1-2, pp 83-86, issn 0022-510X, 4 p.Article

Mitochondrial recessive ataxia syndrome mimicking dominant spinocerebellar ataxiaPALIN, Eino J. H; HAKONEN, Anna H; KORPELA, Mari et al.Journal of the neurological sciences. 2012, Vol 315, Num 1-2, pp 160-163, issn 0022-510X, 4 p.Article

Heredity in multiple system atrophySOMA, Hiroyuki; YABE, Ichiro; TAKEI, Asako et al.Journal of the neurological sciences. 2006, Vol 240, Num 1-2, pp 107-110, issn 0022-510X, 4 p.Article

Meiotic CAG repeat instability in spinocerebellar ataxia type 6 : Maternally transmitted elongation in a presumed sporadic caseLINDQUIST, Suzanne Granhøj; NØRREMOLLE, Anne; HJERMIND, Lena Elisabeth et al.Journal of the neurological sciences. 2006, Vol 241, Num 1-2, pp 95-98, issn 0022-510X, 4 p.Article

Spinocerebellar ataxia type 31 exists in Northeast ChinaYI OUYANG; ZHIYI HE; LEI LI et al.Journal of the neurological sciences. 2012, Vol 316, Num 1-2, pp 164-167, issn 0022-510X, 4 p.Article

Spinocerebellar ataxia type 6 in Mainland China : Molecular and clinical features in four familiesHONG JIANG; BEISHA TANG; KUN XIA et al.Journal of the neurological sciences. 2005, Vol 236, Num 1-2, pp 25-29, issn 0022-510X, 5 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

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

Analysis of SCA8 and SCA12 loci in 134 Italian ataxic patients negative for SCAT-3, 6 and 7 CAG expansionsBRUSCO, Alfredo; CAGNOLI, Claudia; FRANCO, Alessandra et al.Journal of neurology. 2002, Vol 249, Num 7, pp 923-929, issn 0340-5354, 7 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