Samões R - Search Results

1

Female preponderance in genetic generalized epilepsies.

Videira G, Gabriel D, Freitas J, Samões R, Chorão R, Lopes J, Ramalheira J, Lemos C, Leal B, da Silva AM, Chaves J. Videira G, et al. Among authors: samoes r. Seizure. 2021 Oct;91:167-171. doi: 10.1016/j.seizure.2021.06.014. Epub 2021 Jun 16. Seizure. 2021. PMID: 34171625 Free article.

2

The vitamin D receptor gene FokI polymorphism and Multiple Sclerosis in a Northern Portuguese population.

Bettencourt A, Boleixa D, Guimarães AL, Leal B, Carvalho C, Brás S, Samões R, Santos E, Costa PP, Silva B, da Silva AM. Bettencourt A, et al. Among authors: samoes r. J Neuroimmunol. 2017 Aug 15;309:34-37. doi: 10.1016/j.jneuroim.2017.05.005. Epub 2017 May 11. J Neuroimmunol. 2017. PMID: 28601283

3

Circulating microRNAs as potential biomarkers for genetic generalized epilepsies: a three microRNA panel.

Martins-Ferreira R, Chaves J, Carvalho C, Bettencourt A, Chorão R, Freitas J, Samões R, Boleixa D, Lopes J, Ramalheira J, da Silva BM, Martins da Silva A, Costa PP, Leal B. Martins-Ferreira R, et al. Among authors: samoes r. Eur J Neurol. 2020 Apr;27(4):660-666. doi: 10.1111/ene.14129. Epub 2019 Dec 15. Eur J Neurol. 2020. PMID: 31746515

4

Apolipoprotein E isoforms and susceptibility to genetic generalized epilepsies.

Chaves J, Martins-Ferreira R, Carvalho C, Bettencourt A, Brás S, Chorão R, Freitas J, Samões R, Lopes J, Ramalheira J, Silva BM, Pinho E Costa P, da Silva AM, Leal B. Chaves J, et al. Among authors: samoes r. Int J Neurosci. 2020 Sep;130(9):892-897. doi: 10.1080/00207454.2019.1709840. Epub 2020 Jan 6. Int J Neurosci. 2020. PMID: 31877079

5

Social impairment and stigma in genetic generalized epilepsies.

Gabriel D, Ventura M, Samões R, Freitas J, Lopes J, Ramalheira J, Martins da Silva A, Chaves J. Gabriel D, et al. Among authors: samoes r. Epilepsy Behav. 2020 Mar;104(Pt A):106886. doi: 10.1016/j.yebeh.2019.106886. Epub 2020 Jan 11. Epilepsy Behav. 2020. PMID: 31931462

6

Immunogenetic protective factors in Genetic Generalized Epilepsy.

Chaves J, Martins-Ferreira R, Ferreira AM, Brás S, Carvalho C, Bettencourt A, Samões R, Monteiro F, Freitas J, Chorão R, Lopes J, Ramalheira J, da Silva BM, Costa PP, da Silva AM, Leal B. Chaves J, et al. Among authors: samoes r. Epilepsy Res. 2020 Oct;166:106396. doi: 10.1016/j.eplepsyres.2020.106396. Epub 2020 Jun 16. Epilepsy Res. 2020. PMID: 32585211

7

Paraneoplastic neurological syndromes with onconeural antibodies: A single center retrospective study.

Oliveira V, Videira G, Samões R, Carneiro P, Neves E, Santos E. Oliveira V, et al. Among authors: samoes r. J Neurol Sci. 2020 Nov 15;418:117103. doi: 10.1016/j.jns.2020.117103. Epub 2020 Aug 21. J Neurol Sci. 2020. PMID: 32877801

8

Limbic Encephalitis With Positivity for Anti-Flotillin Antibodies in Serum and CSF.

Videira G, Albuquerque L, Oliveira V, Carneiro P, Neves E, Martins da Silva A, Samões R. Videira G, et al. Among authors: samoes r. Neurol Clin Pract. 2021 Feb;11(1):e8-e10. doi: 10.1212/CPJ.0000000000000741. Neurol Clin Pract. 2021. PMID: 33968480 Free PMC article. No abstract available.

9

Depression and anxiety in multiple sclerosis patients: The role of genetic variability of interleukin 1β.

Ferreira AM, Leal B, Ferreira I, Brás S, Moreira I, Samões R, Sousa AP, Santos E, Silva B, Costa PP, Cavaco S, Martins da Silva A. Ferreira AM, et al. Among authors: samoes r. Mult Scler Relat Disord. 2021 Jul;52:102982. doi: 10.1016/j.msard.2021.102982. Epub 2021 Apr 30. Mult Scler Relat Disord. 2021. PMID: 34004436

10

Novel KMT2B mutation causes cerebellar ataxia: Expanding the clinical phenotype.

Damásio J, Santos M, Samões R, Araújo M, Macedo M, Sardoeira A, Cavaco S, Freitas J, Barros J, Oliveira J, Sequeiros J. Damásio J, et al. Among authors: samoes r. Clin Genet. 2021 Dec;100(6):743-747. doi: 10.1111/cge.14055. Epub 2021 Sep 8. Clin Genet. 2021. PMID: 34477219

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