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Page 1
History of settlement of villages from Central Tunisia by studying families sharing a common founder Glycogenosis type III mutation.
Rhouma FB, Messai H, Hsouna S, Halim NB, Cherif W, Fadhel SB, Tiar A, Nagara M, Azzouz H, Sfar MT, Dridi MF, Tebib N, Ayadi A, Abdelhak S, Kefi R. Rhouma FB, et al. Among authors: halim nb. Mitochondrial DNA A DNA Mapp Seq Anal. 2016 Sep;27(5):3194-8. doi: 10.3109/19401736.2015.1007331. Epub 2015 Dec 24. Mitochondrial DNA A DNA Mapp Seq Anal. 2016. PMID: 26704523
Biotinidase deficiency: novel mutations in Algerian patients.
Tiar A, Mekki A, Nagara M, Rhouma FB, Messaoud O, Halim NB, Kefi R, Hamlaoui MT, Lebied A, Abdelhak S. Tiar A, et al. Among authors: halim nb. Gene. 2014 Feb 15;536(1):193-6. doi: 10.1016/j.gene.2013.02.011. Epub 2013 Feb 26. Gene. 2014. PMID: 23481307
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: halim nb. 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