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Page 1
Study of the T16189C variant and mitochondrial lineages in Tunisian and overall Mediterranean region.
Hsouna S, Ben Halim N, Lasram K, Meiloud G, Arfa I, Kerkeni E, Romdhane L, Jamoussi H, Bahri S, Ben Ammar S, Abid A, Barakat A, Houmeida A, Abdelhak S, Kefi R. Hsouna S, et al. Among authors: ben halim n. Mitochondrial DNA A DNA Mapp Seq Anal. 2016;27(2):1558-63. doi: 10.3109/19401736.2014.953136. Epub 2015 Sep 4. Mitochondrial DNA A DNA Mapp Seq Anal. 2016. PMID: 25208176
Mutational founder effect in recessive dystrophic epidermolysis bullosa families from Southern Tunisia.
Ben Brick AS, Laroussi N, Mesrati H, Kefi R, Bchetnia M, Lasram K, Ben Halim N, Romdhane L, Ouragini H, Marrakchi S, Boubaker MS, Meddeb Cherif M, Castiglia D, Hovnanian A, Abdelhak S, Turki H. Ben Brick AS, et al. Among authors: ben halim n. Arch Dermatol Res. 2014 May;306(4):405-11. doi: 10.1007/s00403-013-1421-y. Epub 2013 Oct 30. Arch Dermatol Res. 2014. PMID: 24170138
Contribution of CDKAL1 rs7756992 and IGF2BP2 rs4402960 polymorphisms in type 2 diabetes, diabetic complications, obesity risk and hypertension in the Tunisian population.
Lasram K, Ben Halim N, Benrahma H, Mediene-Benchekor S, Arfa I, Hsouna S, Kefi R, Jamoussi H, Ben Ammar S, Bahri S, Abid A, Benhamamouch S, Barakat A, Abdelhak S. Lasram K, et al. Among authors: ben halim n, ben ammar s. J Diabetes. 2015 Jan;7(1):102-13. doi: 10.1111/1753-0407.12147. Epub 2014 Apr 21. J Diabetes. 2015. PMID: 24636221
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: ben halim n. Hum Hered. 2014;77(1-4):167-74. doi: 10.1159/000362167. Epub 2014 Jul 29. Hum Hered. 2014. PMID: 25060280 Review.
21 results