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Refractory epilepsy in Norrie disease.
Cação G, Garrido C, Miranda V, Pinto-Basto J, Chaves J, Chorão R. Cação G, et al. Among authors: chorao r. Neurol Sci. 2018 Sep;39(9):1631-1633. doi: 10.1007/s10072-018-3428-9. Epub 2018 May 3. Neurol Sci. 2018. PMID: 29725776 No abstract available.
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: chorao 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
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: chorao r. Epilepsy Res. 2020 Oct;166:106396. doi: 10.1016/j.eplepsyres.2020.106396. Epub 2020 Jun 16. Epilepsy Res. 2020. PMID: 32585211
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: chorao 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.
Different relationships between epilepsy syndromes and autoimmune diseases.
Chaves J, Leal B, Sardoeira A, Carvalho V, Samões R, Freitas J, Chorão R, Ferreira AM, Brás S, Lopes J, Ramalheira J, Lemos C, Costa PP, Marinho A, da Silva BM, da Silva AM. Chaves J, et al. Among authors: chorao r. Epileptic Disord. 2023 Feb;25(1):33-44. doi: 10.1002/epd2.20048. Epub 2023 Apr 17. Epileptic Disord. 2023. PMID: 37002555
Familial occipital lobe epilepsy associated with GABAA receptor variants.
Fonte J, Videira G, Chorão R, Freitas J, Carrilho I, Freixo JP, Oliveira J, Chaves J. Fonte J, et al. Among authors: chorao r. Seizure. 2023 Nov;112:139-142. doi: 10.1016/j.seizure.2023.10.003. Epub 2023 Oct 5. Seizure. 2023. PMID: 37852164 No abstract available.
Novel L2HGDH mutations in 21 patients with L-2-hydroxyglutaric aciduria of Portuguese origin.
Vilarinho L, Cardoso ML, Gaspar P, Barbot C, Azevedo L, Diogo L, Santos M, Carrilho I, Fineza I, Kok F, Chorão R, Alegria P, Martins E, Teixeira J, Cabral Fernandes H, Verhoeven NM, Salomons GS, Santorelli FM, Cabral P, Amorim A, Jakobs C. Vilarinho L, et al. Among authors: chorao r. Hum Mutat. 2005 Oct;26(4):395-6. doi: 10.1002/humu.9373. Hum Mutat. 2005. PMID: 16134148
21 results