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Neonatal screening for spinal muscular atrophy: A pilot study in Brazil.
Oliveira Netto AB, Brusius-Facchin AC, Lemos JF, Pasetto FB, Brasil CS, Trapp FB, Saute JAM, Donis KC, Becker MM, Wiest P, Coutinho VLS, Castro S, Ferreira J, Silveira C, Bittar MFR, Wang C, Lana JM, França Junior MC, Giugliani R. Oliveira Netto AB, et al. Among authors: becker mm. Genet Mol Biol. 2023 Dec 11;46(3 Suppl 1):e20230126. doi: 10.1590/1678-4685-GMB-2023-0126. eCollection 2023. Genet Mol Biol. 2023. PMID: 38091267 Free PMC article.
Consensus from the Brazilian Academy of Neurology for the diagnosis, genetic counseling, and use of disease-modifying therapies in 5q spinal muscular atrophy.
Zanoteli E, Araujo APQC, Becker MM, Fortes CPDD, França MC Jr, Machado-Costa MC, Marques W Jr, Matsui C Jr, Mendonça RH, Nardes F, Oliveira ASB, Pessoa ALS, Saute JAM, Sgobbi P, Van der Linden H Jr, Gurgel-Giannetti J. Zanoteli E, et al. Among authors: becker mm. Arq Neuropsiquiatr. 2024 Jan;82(1):1-18. doi: 10.1055/s-0044-1779503. Epub 2024 Feb 5. Arq Neuropsiquiatr. 2024. PMID: 38316428 Free PMC article.
Intragenic variants in the SMN1 gene determine the clinical phenotype in 5q spinal muscular atrophy.
Mendonça RH, Matsui C Jr, Polido GJ, Silva AMS, Kulikowski L, Torchio Dias A, Zanardo EA, Solla DJF, Gurgel-Giannetti J, de Moura ACML, Sampaio GPC, Oliveira ASB, de Souza PVS, Pinto WBVR, Gonçalves EA, Farias IB, Nardes F, Araújo APQC, Marques W Jr, Tomaselli PJ, Ribeiro MDO, Kitajima JP, Paoli Monteiro F, Saute JAM, Becker MM, Saraiva-Pereira ML, Brusius-Facchin AC, van der Linden V, Florêncio RN, Barbosa AVS, Machado-Costa MC, Pessoa ALS, Souza LS, Franca MC Jr, Kok F, Reed UC, Zanoteli E. Mendonça RH, et al. Among authors: becker mm. Neurol Genet. 2020 Sep 1;6(5):e505. doi: 10.1212/NXG.0000000000000505. eCollection 2020 Oct. Neurol Genet. 2020. PMID: 33062891 Free PMC article.
Genetic profile of Brazilian patients with dystrophinopathies.
de Almeida PAD, Machado-Costa MC, Manzoli GN, Ferreira LS, Rodrigues MCS, Bueno LSM, Saute JAM, Pinto Vairo F, Matte US, Siebert M, Cossio SL, Macedo GS, Winckler PB, Becker MM, Magalhães LVB, Gonçalves MVM, Marrone CD, Nucci A, França MC Jr. de Almeida PAD, et al. Among authors: becker mm. Clin Genet. 2017 Aug;92(2):199-203. doi: 10.1111/cge.12975. Epub 2017 Feb 22. Clin Genet. 2017. PMID: 28116794
Evidence for Association Between OXTR Gene and ASD Clinical Phenotypes.
de Oliveira Pereira Ribeiro L, Vargas-Pinilla P, Kappel DB, Longo D, Ranzan J, Becker MM, Dos Santos Riesgo R, Schuler-Faccini L, Roman T, Schuch JB. de Oliveira Pereira Ribeiro L, et al. Among authors: becker mm. J Mol Neurosci. 2018 Jun;65(2):213-221. doi: 10.1007/s12031-018-1088-0. Epub 2018 Jun 1. J Mol Neurosci. 2018. PMID: 29858823
Treatment of refractory neonatal seizures with topiramate.
Riesgo R, Winckler MI, Ohlweiler L, Ranzan J, Becker M, Salvador S, Magalhaes L, Ribeiro R. Riesgo R, et al. Neuropediatrics. 2012 Dec;43(6):353-6. doi: 10.1055/s-0032-1327771. Epub 2012 Sep 24. Neuropediatrics. 2012. PMID: 23007795
Post-H1N1 vaccine acute disseminated encephalomyelitis.
Becker MM, Ranzan J, Magalhães LV, Ohlweiler L, Winckler MI, Ramos MS, Riesgo R. Becker MM, et al. Pediatr Int. 2014 Jun;56(3):437-8. doi: 10.1111/ped.12148. Pediatr Int. 2014. PMID: 24894935 No abstract available.
88 results