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Association of genetic variants in the FTO gene with metabolic syndrome: A case-control study in the Tunisian population.
Elouej S, Nagara M, Attaoua R, Sallem OK, Rejeb I, Hsouna S, Lasram K, Halim NB, Chargui M, Jamoussi H, Turki Z, Kamoun I, Belfki-Benali H, Abid A, Slama CB, Bahri S, Triki D, Romdhane HB, Abdelhak S, Kefi R, Grigorescu F. Elouej S, et al. Among authors: rejeb i. J Diabetes Complications. 2016 Mar;30(2):206-11. doi: 10.1016/j.jdiacomp.2015.11.013. Epub 2015 Nov 14. J Diabetes Complications. 2016. PMID: 26700404
Specific aspects of consanguinity: some examples from the Tunisian population.
Romdhane L, Ben Halim N, Rejeb I, Kefi R, Bouyacoub Y, Ben Rekaya M, Messai H, Messaoud O, Riahi Z, Bonnet C, Ben Rhouma F, Nagara M, Petit C, McElreavey K, Romeo G, Abdelhak S. Romdhane L, et al. Among authors: rejeb i. Hum Hered. 2014;77(1-4):167-74. doi: 10.1159/000362167. Epub 2014 Jul 29. Hum Hered. 2014. PMID: 25060280 Free article. Review.
Differential impact of consanguineous marriages on autosomal recessive diseases in Tunisia.
Ben Halim N, Hsouna S, Lasram K, Rejeb I, Walha A, Talmoudi F, Messai H, Sabrine Ben Brick A, Ouragini H, Cherif W, Nagara M, Ben Rhouma F, Chouchene I, Ouechtati F, Bouyacoub Y, Ben Rekaya M, Messaoud O, Ben Ammar S, El Matri L, Tebib N, Ben Dridi MF, Mokni M, Amouri A, Kefi R, Abdelhak S. Ben Halim N, et al. Among authors: rejeb i. Am J Hum Biol. 2016 Mar-Apr;28(2):171-80. doi: 10.1002/ajhb.22764. Epub 2015 Jul 16. Am J Hum Biol. 2016. PMID: 26179682
Absent meibomian glands and cone dystrophy in ADULT syndrome: identification by whole exome sequencing of pathogenic variants in two causal genes TP63 and CNGB3.
Hizem S, Maamouri R, Zaouak A, Rejeb I, Karoui S, Sebai M, Jilani H, Elaribi Y, Fenniche S, Cheour M, Bilan F, Ben Jemaa L. Hizem S, et al. Among authors: rejeb i. Ophthalmic Genet. 2024 Feb;45(1):84-94. doi: 10.1080/13816810.2023.2206891. Epub 2023 May 9. Ophthalmic Genet. 2024. PMID: 37158316
Man-O-War simulator: a Low-cost manikin for training on chest tube management.
Nasri A, Jerbi M, Karray R, Snoussi H, Samet A, Talbi A, Ksentini H, Rejeb I, Chakroun-Walha O, Rekik N. Nasri A, et al. Among authors: rejeb i. Afr J Emerg Med. 2023 Jun;13(2):39-41. doi: 10.1016/j.afjem.2023.01.004. Epub 2023 Feb 17. Afr J Emerg Med. 2023. PMID: 36864887 Free PMC article.
Craniofacial Malformations as Fundamental Diagnostic Tools in Syndromic Entities.
Al Kaissi A, Ryabykh S, Nassib N, Bouchoucha S, Benjemaa L, Rejeb I, Hizem S, Kenis V, Grill F, Kircher SG, Shboul M, Ben Chehida F. Al Kaissi A, et al. Among authors: rejeb i. Diagnostics (Basel). 2022 Sep 30;12(10):2375. doi: 10.3390/diagnostics12102375. Diagnostics (Basel). 2022. PMID: 36292064 Free PMC article.
43 results