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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. Cerebellum. 2015 Dec;14(6):728-30. doi: 10.1007/s12311-015-0666-8. Cerebellum. 2015. PMID: 25869926 No abstract available.
Alpha-fetoprotein as a biomarker for recessive ataxias.
Braga-Neto P, Dutra LA, Pedroso JL, Barsottini OG. Braga-Neto P, et al. Arq Neuropsiquiatr. 2010 Dec;68(6):953-5. doi: 10.1590/s0004-282x2010000600022. Arq Neuropsiquiatr. 2010. PMID: 21243258 Free article. No abstract available.
Sleep disorders in cerebellar ataxias.
Pedroso JL, Braga-Neto P, Felício AC, Aquino CC, Prado LB, Prado GF, Barsottini OG. Pedroso JL, et al. Arq Neuropsiquiatr. 2011 Apr;69(2A):253-7. doi: 10.1590/s0004-282x2011000200021. Arq Neuropsiquiatr. 2011. PMID: 21537570 Free article. Review.
SCA2 presenting as an ataxia-parkinsonism-motor neuron disease syndrome.
Braga-Neto P, Pedroso JL, Felício AC, Abrahão A, Dutra LA, Bezerra ML, Barsottini OG. Braga-Neto P, et al. Arq Neuropsiquiatr. 2011;69(2B):405-6. doi: 10.1590/s0004-282x2011000300027. Arq Neuropsiquiatr. 2011. PMID: 21625775 Free article. No abstract available.
Akathisia: An unusual movement disorder in Machado-Joseph disease.
Pedroso JL, Braga-Neto P, Felício AC, Barsottini OG, Jardim LB, Saraiva-Pereira ML. Pedroso JL, et al. Parkinsonism Relat Disord. 2011 Nov;17(9):712-3. doi: 10.1016/j.parkreldis.2011.05.011. Epub 2011 Jun 24. Parkinsonism Relat Disord. 2011. PMID: 21703908 No abstract available.
142 results