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Next-generation sequencing of Tunisian Leigh syndrome patients reveals novel variations: impact for diagnosis and treatment.
Hechmi M, Charif M, Kraoua I, Fassatoui M, Dallali H, Desquiret-Dumas V, Bris C, Goudenège D, Drissi C, Galaï S, Ouerhani S, Procaccio V, Amati-Bonneau P, Abdelhak S, Ben Youssef-Turki I, Lenaers G, Kefi R. Hechmi M, et al. Among authors: ben youssef turki i. Biosci Rep. 2022 Sep 30;42(9):BSR20220194. doi: 10.1042/BSR20220194. Biosci Rep. 2022. PMID: 36093993 Free PMC article.
Childhood opsoclonus-myoclonus syndrome: A case series from Tunisia.
Ben Achour N, Mrabet S, Rebai I, Abid I, Benrhouma H, Klaa H, Rouissi A, Kraoua I, Ben Youssef Turki I. Ben Achour N, et al. Brain Dev. 2017 Oct;39(9):751-755. doi: 10.1016/j.braindev.2017.05.001. Epub 2017 May 23. Brain Dev. 2017. PMID: 28549713
Autoimmune Encephalitis in Tunisia: Report of a Pediatric Cohort.
Douma B, Ben Younes T, Benrhouma H, Miladi Z, Zamali I, Rouissi A, Klaa H, Kraoua I, Ben Ahmed M, Ben Youssef Turki I. Douma B, et al. Among authors: ben youssef turki i. J Immunol Res. 2021 May 10;2021:6666117. doi: 10.1155/2021/6666117. eCollection 2021. J Immunol Res. 2021. PMID: 34056010 Free PMC article.
31 results