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Recent developments in the genetics of childhood epileptic encephalopathies: impact in clinical practice.
Arq Neuropsiquiatr. 2015 Nov;73(11):946-58. doi: 10.1590/0004-282X20150122. Epub 2015 Oct 6.
Arq Neuropsiquiatr. 2015.
PMID: 26517219
Free article.
Review.
Revisiting the clinical impact of variants in EFHC1 in patients with different phenotypes of genetic generalized epilepsy.
Gonsales MC, Ribeiro PAO, Betting LE, Alvim MKM, Guerreiro CM, Yasuda CL, Gitaí DLG, Cendes F, Lopes-Cendes I.
Gonsales MC, et al.
Epilepsy Behav. 2020 Nov;112:107469. doi: 10.1016/j.yebeh.2020.107469. Epub 2020 Sep 29.
Epilepsy Behav. 2020.
PMID: 33181902
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Multimodal Analysis of SCN1A Missense Variants Improves Interpretation of Clinically Relevant Variants in Dravet Syndrome.
Gonsales MC, Montenegro MA, Preto P, Guerreiro MM, Coan AC, Quast MP, Carvalho BS, Lopes-Cendes I.
Gonsales MC, et al.
Front Neurol. 2019 Mar 28;10:289. doi: 10.3389/fneur.2019.00289. eCollection 2019.
Front Neurol. 2019.
PMID: 31001185
Free PMC article.
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Genetic variability in COVID-19-related genes in the Brazilian population.
Secolin R, de Araujo TK, Gonsales MC, Rocha CS, Naslavsky M, Marco L, Bicalho MAC, Vazquez VL, Zatz M, Silva WA, Lopes-Cendes I.
Secolin R, et al. Among authors: gonsales mc.
Hum Genome Var. 2021 Apr 2;8:15. doi: 10.1038/s41439-021-00146-w. eCollection 2021.
Hum Genome Var. 2021.
PMID: 33824725
Free PMC article.
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Exploring a Region on Chromosome 8p23.1 Displaying Positive Selection Signals in Brazilian Admixed Populations: Additional Insights Into Predisposition to Obesity and Related Disorders.
Secolin R, Gonsales MC, Rocha CS, Naslavsky M, De Marco L, Bicalho MAC, Vazquez VL, Zatz M, Silva WA, Lopes-Cendes I.
Secolin R, et al. Among authors: gonsales mc.
Front Genet. 2021 Mar 25;12:636542. doi: 10.3389/fgene.2021.636542. eCollection 2021.
Front Genet. 2021.
PMID: 33841501
Free PMC article.
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