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Comorbidity in the Tunisian population.
Romdhane L, Messaoud O, Bouyacoub Y, Kerkeni E, Naouali C, Cherif Ben Abdallah L, Tiar A, Charfeddine C, Monastiri K, Chabchoub I, Hachicha M, Tadmouri GO, Romeo G, Abdelhak S. Romdhane L, et al. Among authors: tiar a. Clin Genet. 2016 Mar;89(3):312-9. doi: 10.1111/cge.12616. Epub 2015 Jun 10. Clin Genet. 2016. PMID: 26010040
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. Gene. 2014 Feb 15;536(1):193-6. doi: 10.1016/j.gene.2013.02.011. Epub 2013 Feb 26. Gene. 2014. PMID: 23481307
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: tiar a. 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
Vitamin B-complex deficiency and visual acuity.
Damodaran M, Rameshwar Sarma KV, Tiar A, Nadamuni Naidu A. Damodaran M, et al. Among authors: tiar a. Br J Nutr. 1979 Jan;41(1):27-30. doi: 10.1079/bjn19790007. Br J Nutr. 1979. PMID: 420756 Clinical Trial.