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Page 1
A systematic review of adults with Dravet syndrome.
Selvarajah A, Zulfiqar-Ali Q, Marques P, Rong M, Andrade DM. Selvarajah A, et al. Among authors: zulfiqar ali q. Seizure. 2021 Apr;87:39-45. doi: 10.1016/j.seizure.2021.02.025. Epub 2021 Feb 22. Seizure. 2021. PMID: 33677403 Free article. Review.
Genome sequencing identifies rare tandem repeat expansions and copy number variants in Lennox-Gastaut syndrome.
Qaiser F, Sadoway T, Yin Y, Zulfiqar Ali Q, Nguyen CM, Shum N, Backstrom I, Marques PT, Tabarestani S, Munhoz RP, Krings T, Pearson CE, Yuen RKC, Andrade DM. Qaiser F, et al. Among authors: zulfiqar ali q. Brain Commun. 2021 Sep 14;3(3):fcab207. doi: 10.1093/braincomms/fcab207. eCollection 2021. Brain Commun. 2021. PMID: 34622207 Free PMC article.
Adult Phenotype of SYNGAP1-DEE.
Rong M, Benke T, Zulfiqar Ali Q, Aledo-Serrano Á, Bayat A, Rossi A, Devinsky O, Qaiser F, Ali AS, Fasano A, Bassett AS, Andrade DM. Rong M, et al. Among authors: zulfiqar ali q. Neurol Genet. 2023 Nov 17;9(6):e200105. doi: 10.1212/NXG.0000000000200105. eCollection 2023 Dec. Neurol Genet. 2023. PMID: 38045990 Free PMC article.
Adult Phenotype of CHD2-Associated Disorders.
Rong M, Zulfiqar Ali Q, Aledo-Serrano A, Bayat A, Devinsky O, Qaiser F, Chandran I, Ali A, Fasano A, Bassett AS, Andrade DM. Rong M, et al. Among authors: zulfiqar ali q. Neurol Genet. 2024 Nov 25;10(6):e200194. doi: 10.1212/NXG.0000000000200194. eCollection 2024 Dec. Neurol Genet. 2024. PMID: 39601014 Free PMC article.
Do germline genetic variants influence surgical outcomes in drug-resistant epilepsy?
Marques P, Moloney PB, Ji C, Zulfiqar Ali Q, Ramesh A, Goldstein DB, Barboza K, Chandran I, Rong M, Selvarajah A, Qaiser F, Lira VST, Valiante TA, Bazil CW, Choi H, Devinsky O, Depondt C, O'Brien T, Perucca P, Sen A, Dugan P, Sands TT, Delanty N, Andrade DM. Marques P, et al. Among authors: zulfiqar ali q. Epilepsy Res. 2024 Oct;206:107425. doi: 10.1016/j.eplepsyres.2024.107425. Epub 2024 Aug 6. Epilepsy Res. 2024. PMID: 39168079
11 results