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Page 1
Normal ATXN3 Allele but Not CHIP Polymorphisms Modulates Age at Onset in Machado-Joseph Disease.
França MC Jr, Emmel VE, D'Abreu A, Maurer-Morelli CV, Secolin R, Bonadia LC, da Silva MS, Nucci A, Jardim LB, Saraiva-Pereira ML, Marques W Jr, Paulson H, Lopes-Cendes I. França MC Jr, et al. Among authors: bonadia lc. Front Neurol. 2012 Nov 19;3:164. doi: 10.3389/fneur.2012.00164. eCollection 2012. Front Neurol. 2012. PMID: 23181052 Free PMC article.
The frequency of the C9orf72 expansion in a Brazilian population.
Cintra VP, Bonadia LC, Andrade HMT, de Albuquerque M, Eusébio MF, de Oliveira DS, Claudino R, Gonçalves MVM, Teixeira AL Jr, de Godoy Rousseff Prado L, de Souza LC, Dourado MET Jr, Oliveira ASB, Tumas V, França MC Jr, Marques W Jr. Cintra VP, et al. Among authors: bonadia lc. Neurobiol Aging. 2018 Jun;66:179.e1-179.e4. doi: 10.1016/j.neurobiolaging.2018.01.007. Epub 2018 Jan 31. Neurobiol Aging. 2018. PMID: 29449030
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. Among authors: bonadia lc. 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
CAG repeats ≥ 34 in Ataxin-1 gene are associated with amyotrophic lateral sclerosis in a Brazilian cohort.
Gonçalves JPN, de Andrade HMT, Cintra VP, Bonadia LC, Leoni TB, de Albuquerque M, Martins MP, de Borba FC, Couteiro RED, de Oliveira DS, Claudino R, Gonçalves MVM, Dourado ME, de Souza LC, Teixeira AL, de Godoy Rousseff Prado L, Tumas V, Oliveira ASB, Nucci A, Lopes-Cendes I, Marques W Jr, França MC Jr. Gonçalves JPN, et al. Among authors: bonadia lc. J Neurol Sci. 2020 Jul 15;414:116842. doi: 10.1016/j.jns.2020.116842. Epub 2020 Apr 19. J Neurol Sci. 2020. PMID: 32339968
Dopa-Responsive Parkinsonism in a Patient With Homozygous RFC1 Expansions.
da Silva Schmitt G, Martinez ARM, da Graça FF, de Lima FD, Bonadia LC, Amorim BJ, Nucci A, França MC Jr. da Silva Schmitt G, et al. Among authors: bonadia lc. Mov Disord. 2020 Oct;35(10):1889-1890. doi: 10.1002/mds.28286. Mov Disord. 2020. PMID: 33068476 No abstract available.
Diagnostic Yield of Whole Exome Sequencing for Adults with Ataxia: a Brazilian Perspective.
da Graça FF, Peluzzo TM, Bonadia LC, Martinez ARM, Diniz de Lima F, Pedroso JL, Barsottini OGP, Gama MTD, Akçimen F, Dion PA, Rouleau GA, Marques W Jr, França MC Jr. da Graça FF, et al. Among authors: bonadia lc. Cerebellum. 2022 Feb;21(1):49-54. doi: 10.1007/s12311-021-01268-1. Epub 2021 May 6. Cerebellum. 2022. PMID: 33956305
Brain Structural Signature of RFC1-Related Disorder.
Matos PCAAP, Rezende TJR, Schmitt GS, Bonadia LC, Reis F, Martinez ARM, de Lima FD, Bueno MGA, Tomaselli PJ, Cendes F, Pedroso JL, Barsottini OGP, Marques W Jr, França M Jr. Matos PCAAP, et al. Among authors: bonadia lc. Mov Disord. 2021 Nov;36(11):2634-2641. doi: 10.1002/mds.28711. Epub 2021 Jul 9. Mov Disord. 2021. PMID: 34241918
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