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Comorbidity in the Tunisian population.
Clin Genet. 2016 Mar;89(3):312-9. doi: 10.1111/cge.12616. Epub 2015 Jun 10.
Clin Genet. 2016.
PMID: 26010040
Mutation spectrum of primary hyperoxaluria type 1 in Tunisia: implication for diagnosis in North Africa.
Nagara M, Tiar A, Ben Halim N, Ben Rhouma F, Messaoud O, Bouyacoub Y, Kefi R, Hassayoun S, Zouari N, Ben Ammar MS, Abdelhak S, Chemli J.
Nagara M, et al. Among authors: tiar a.
Gene. 2013 Sep 15;527(1):316-20. doi: 10.1016/j.gene.2013.06.023. Epub 2013 Jun 25.
Gene. 2013.
PMID: 23810941
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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
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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
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Impact of parental acquired brain injury on children: Review of the literature and conceptual model.
Tiar AM, Dumas JE.
Tiar AM, et al.
Brain Inj. 2015;29(9):1005-17. doi: 10.3109/02699052.2014.976272. Epub 2015 Jul 16.
Brain Inj. 2015.
PMID: 26182231
Review.
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A study survey on intestinal and blood parasites among school children in Sana'a province, Yemen.
Azazy AA, Al-Tiar AS.
Azazy AA, et al. Among authors: al tiar as.
Saudi Med J. 1999 Jun;20(6):422-4.
Saudi Med J. 1999.
PMID: 27632648
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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.
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