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Page 1
Neurological phenotypes in spinocerebellar ataxia type 2: Role of mitochondrial polymorphism A10398G and other risk factors.
Monte TL, Pereira FS, Reckziegel EDR, Augustin MC, Locks-Coelho LD, Santos ASP, Pedroso JL, Barsottini O, Vargas FR, Saraiva-Pereira ML, Jardim LB; Rede Neurogenética. Monte TL, et al. Among authors: barsottini o. Parkinsonism Relat Disord. 2017 Sep;42:54-60. doi: 10.1016/j.parkreldis.2017.06.010. Epub 2017 Jun 19. Parkinsonism Relat Disord. 2017. PMID: 28648514
ATXN3, ATXN7, CACNA1A, and RAI1 Genes and Mitochondrial Polymorphism A10398G Did Not Modify Age at Onset in Spinocerebellar Ataxia Type 2 Patients from South America.
Pereira FS, Monte TL, Locks-Coelho LD, Silva AS, Barsottini O, Pedroso JL, Cornejo-Olivas M, Mazzetti P, Godeiro C, Vargas FR, Lima MA, van der Linden H Jr, Toralles MB, Medeiros PF, Ribeiro E, Braga-Neto P, Salarini D, Castilhos RM, Saraiva-Pereira ML, Jardim LB; Rede Neurogenetica. Pereira FS, et al. Among authors: barsottini o. Cerebellum. 2015 Dec;14(6):728-30. doi: 10.1007/s12311-015-0666-8. Cerebellum. 2015. PMID: 25869926 No abstract available.
Selective Forces Related to Spinocerebellar Ataxia Type 2.
Sena LS, Castilhos RM, Mattos EP, Furtado GV, Pedroso JL, Barsottini O, de Amorim MMP, Godeiro C, Pereira MLS, Jardim LB. Sena LS, et al. Among authors: barsottini o. Cerebellum. 2019 Apr;18(2):188-194. doi: 10.1007/s12311-018-0977-7. Cerebellum. 2019. PMID: 30219976
Huntington disease and Huntington disease-like in a case series from Brazil.
Castilhos RM, Souza AF, Furtado GV, Gheno TC, Silva AL, Vargas FR, Lima MA, Barsottini O, Pedroso JL, Godeiro C Jr, Salarini D, Pereira ET, Lin K, Toralles MB, Saute JA, Rieder CR, Quintas M, Sequeiros J, Alonso I, Saraiva-Pereira ML, Jardim LB. Castilhos RM, et al. Among authors: barsottini o. Clin Genet. 2014 Oct;86(4):373-7. doi: 10.1111/cge.12283. Epub 2013 Oct 17. Clin Genet. 2014. PMID: 24102565
Spinocerebellar ataxia type 10: common haplotype and disease progression rate in Peru and Brazil.
Gheno TC, Furtado GV, Saute JAM, Donis KC, Fontanari AMV, Emmel VE, Pedroso JL, Barsottini O, Godeiro-Junior C, van der Linden H, Ternes Pereira E, Cintra VP, Marques W Jr, de Castilhos RM, Alonso I, Sequeiros J, Cornejo-Olivas M, Mazzetti P, Leotti VB, Jardim LB, Saraiva-Pereira ML; Rede Neurogenetica. Gheno TC, et al. Among authors: barsottini o. Eur J Neurol. 2017 Jul;24(7):892-e36. doi: 10.1111/ene.13281. Epub 2017 May 31. Eur J Neurol. 2017. PMID: 28560845
Polysomnography findings in spinocerebellar ataxia type 6.
Rueda AD, Pedroso JL, Truksinas E, Do Prado GF, Coelho FM, Barsottini OG. Rueda AD, et al. J Sleep Res. 2016 Dec;25(6):720-723. doi: 10.1111/jsr.12439. Epub 2016 Jul 5. J Sleep Res. 2016. PMID: 27377205
Spinocerebellar ataxias in Brazil--frequencies and modulating effects of related genes.
de Castilhos RM, Furtado GV, Gheno TC, Schaeffer P, Russo A, Barsottini O, Pedroso JL, Salarini DZ, Vargas FR, de Lima MA, Godeiro C, Santana-da-Silva LC, Toralles MB, Santos S, van der Linden H Jr, Wanderley HY, de Medeiros PF, Pereira ET, Ribeiro E, Saraiva-Pereira ML, Jardim LB; Rede Neurogenetica. de Castilhos RM, et al. Among authors: barsottini o. Cerebellum. 2014 Feb;13(1):17-28. doi: 10.1007/s12311-013-0510-y. Cerebellum. 2014. PMID: 23943520
Correction to: Selective Forces Related to Spinocerebellar Ataxia Type 2.
Sena LS, Castilhos RM, Mattos EP, Furtado GV, Pedroso JL, Barsottini O, de Amorim MMP, Godeiro C, Saraiva-Pereira ML, Jardim LB. Sena LS, et al. Among authors: barsottini o. Cerebellum. 2019 Apr;18(2):195. doi: 10.1007/s12311-018-0991-9. Cerebellum. 2019. PMID: 30450503
330 results