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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.
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.