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Spinocerebellar ataxia type 2 has multiple ancestral origins.
Sena LS, Furtado GV, Pedroso JL, Barsottini O, Cornejo-Olivas M, Nóbrega PR, Braga Neto P, Soares DMB, Vargas FR, Godeiro C, Medeiros PFV, Camejo C, Toralles MBP, Fagundes NJR, Jardim LB, Saraiva-Pereira ML; Rede Neurogenetica. Sena LS, et al. Among authors: furtado gv. Parkinsonism Relat Disord. 2024 Mar;120:105985. doi: 10.1016/j.parkreldis.2023.105985. Epub 2023 Dec 31. Parkinsonism Relat Disord. 2024. PMID: 38181536
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: furtado gv. Cerebellum. 2019 Apr;18(2):188-194. doi: 10.1007/s12311-018-0977-7. Cerebellum. 2019. PMID: 30219976
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: furtado gv. Cerebellum. 2014 Feb;13(1):17-28. doi: 10.1007/s12311-013-0510-y. Cerebellum. 2014. PMID: 23943520
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: furtado gv. Eur J Neurol. 2017 Jul;24(7):892-e36. doi: 10.1111/ene.13281. Epub 2017 May 31. Eur J Neurol. 2017. PMID: 28560845
Haplotype Study in SCA10 Families Provides Further Evidence for a Common Ancestral Origin of the Mutation.
Bampi GB, Bisso-Machado R, Hünemeier T, Gheno TC, Furtado GV, Veliz-Otani D, Cornejo-Olivas M, Mazzeti P, Bortolini MC, Jardim LB, Saraiva-Pereira ML; Rede Neurogenetica. Bampi GB, et al. Among authors: furtado gv. Neuromolecular Med. 2017 Dec;19(4):501-509. doi: 10.1007/s12017-017-8464-8. Epub 2017 Sep 13. Neuromolecular Med. 2017. PMID: 28905220
The progression rate of spinocerebellar ataxia type 2 changes with stage of disease.
Monte TL, Reckziegel EDR, Augustin MC, Locks-Coelho LD, Santos ASP, Furtado GV, de Mattos EP, Pedroso JL, Barsottini OP, Vargas FR, Saraiva-Pereira ML, Camey SA, Leotti VB, Jardim LB; Rede Neurogenética. Monte TL, et al. Among authors: furtado gv. Orphanet J Rare Dis. 2018 Jan 25;13(1):20. doi: 10.1186/s13023-017-0725-y. Orphanet J Rare Dis. 2018. PMID: 29370806 Free PMC article.
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: furtado gv. Cerebellum. 2019 Apr;18(2):195. doi: 10.1007/s12311-018-0991-9. Cerebellum. 2019. PMID: 30450503
35 results