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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2009 1
2012 1
2014 2
2017 1
2018 2
2019 1
2020 2
2021 2
2022 2
2023 1
2024 1

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15 results

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Page 1
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
RFC1-Related Disorder: In Vivo Evaluation of Spinal Cord Damage.
Rezende TJR, Schmitt GS, de Lima FD, de Brito MR, Matos PCAAP, Bonadia LC, Martinez ARM, Cendes F, Pedroso JL, Barsottini OGP, Marques W Jr, França MC Jr. Rezende TJR, et al. Among authors: bonadia lc. Mov Disord. 2022 Oct;37(10):2122-2128. doi: 10.1002/mds.29169. Epub 2022 Jul 25. Mov Disord. 2022. PMID: 35877029
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
22q11.2 Deletion Syndrome: Influence of Parental Origin on Clinical Heterogeneity.
de Wallau MB, Xavier AC, Moreno CA, Kim CA, Mendes EL, Ribeiro EM, Oliveira A, Félix TM, Fett-Conte AC, Bonadia LC, Correia-Costa GR, Monlleó IL, Gil-da-Silva-Lopes VL, Vieira TP. de Wallau MB, et al. Among authors: bonadia lc. Genes (Basel). 2024 Apr 21;15(4):518. doi: 10.3390/genes15040518. Genes (Basel). 2024. PMID: 38674452 Free PMC article.
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
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
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
15 results