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2013 1
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2016 5
2017 1
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Page 1
The expanding clinical and genetic spectrum of alsin-related disorders: the first cohort of Brazilian patients.
Alves De Siqueira Carvalho A, Antônio Troccoli Chieia M, Braga Farias I, Bulle Oliveira AS, Pinto WBVR, Souza PVS. Alves De Siqueira Carvalho A, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2022 Feb;23(1-2):16-24. doi: 10.1080/21678421.2021.1910306. Epub 2021 Nov 5. Amyotroph Lateral Scler Frontotemporal Degener. 2022. PMID: 34738851 Review.
DRPLA: An unusual disease or an underestimated cause of ataxia in Brazil?
Pinto WBVR, Salomão RPA, Bergamasco NC, da Cunha Ribas G, da Graça FF, Lopes-Cendes I, Bonadia L, de Souza PVS, Bulle Oliveira AS, Saraiva-Pereira ML, Jardim LB, Tumas V, Junior WM, França MC Jr, Pedroso JL, Barsottini OGP, Teive HAG. Pinto WBVR, et al. Parkinsonism Relat Disord. 2021 Nov;92:67-71. doi: 10.1016/j.parkreldis.2021.10.004. Epub 2021 Oct 11. Parkinsonism Relat Disord. 2021. PMID: 34700111
Mutation in PNKP presenting initially as axonal Charcot-Marie-Tooth disease.
Pedroso JL, Rocha CR, Macedo-Souza LI, De Mario V, Marques W Jr, Barsottini OG, Bulle Oliveira AS, Menck CF, Kok F. Pedroso JL, et al. Among authors: bulle oliveira as. Neurol Genet. 2015 Oct 22;1(4):e30. doi: 10.1212/NXG.0000000000000030. eCollection 2015 Dec. Neurol Genet. 2015. PMID: 27066567 Free PMC article.
Intermediate-length CAG repeat in ATXN2 is associated with increased risk for amyotrophic lateral sclerosis in Brazilian patients.
Tavares de Andrade HM, Cintra VP, de Albuquerque M, Piccinin CC, Bonadia LC, Duarte Couteiro RE, Sabino de Oliveira D, Claudino R, Magno Gonçalves MV, Dourado MET Jr, de Souza LC, Teixeira AL, de Godoy Rousseff Prado L, Tumas V, Bulle Oliveira AS, Nucci A, Lopes-Cendes I, Marques W Jr, França MC Jr. Tavares de Andrade HM, et al. Neurobiol Aging. 2018 Sep;69:292.e15-292.e18. doi: 10.1016/j.neurobiolaging.2018.04.020. Epub 2018 May 8. Neurobiol Aging. 2018. PMID: 29934271
16 results