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Page 1
Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity.
Messaoud O, Rekaya MB, Ouragini H, Benfadhel S, Azaiez H, Kefi R, Gouider-Khouja N, Mokhtar I, Amouri A, Boubaker MS, Zghal M, Abdelhak S. Messaoud O, et al. Among authors: amouri a. Arch Dermatol Res. 2012 Mar;304(2):171-6. doi: 10.1007/s00403-011-1190-4. Epub 2011 Nov 12. Arch Dermatol Res. 2012. PMID: 22081045
The experience of a Tunisian referral centre in prenatal diagnosis of Xeroderma pigmentosum.
Messaoud O, Ben Rekaya M, Jerbi M, Ouertani I, Kefi R, Laroussi N, Bouyacoub Y, Benfadhel S, Yacoub-Youssef H, Boubaker S, Zghal M, Mrad R, Amouri A, Abdelhak S. Messaoud O, et al. Among authors: amouri a. Public Health Genomics. 2013;16(5):251-4. doi: 10.1159/000354584. Epub 2013 Sep 7. Public Health Genomics. 2013. PMID: 24021614
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: amouri a. 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
High frequency of exon 15 deletion in the FANCA gene in Tunisian patients affected with Fanconi anemia disease: implication for diagnosis.
Amouri A, Talmoudi F, Messaoud O, d'Enghien CD, Rekaya MB, Allegui I, Azaiez H, Kefi R, Abdelhak A, Meseddi SH, Torjemane L, Ouederni M, Mellouli F, Abid HB, Aissaoui L, Bejaoui M, Othmen TB, Lyonnet DS, Soulier J, Hachicha M, Dellagi K, Abdelhak S, Fanconi T. Amouri A, et al. Mol Genet Genomic Med. 2014 Mar;2(2):160-5. doi: 10.1002/mgg3.55. Epub 2014 Feb 5. Mol Genet Genomic Med. 2014. PMID: 24689079 Free PMC article.
Cytogenetic assessment of Fanconi anemia in children with aplastic anemia in Tunisia.
Talmoudi F, Kammoun L, Benhalim N, Torjemane L, Ouederni M, Aissaoui L, Lakhal A, Mellouli F, Othmen TB, Bejaoui M, Abdelhak S, Meddeb M, Dellagi K, Hdiji S, Amouri A; Tunisian Fanconi Anemia Study Group. Talmoudi F, et al. Among authors: amouri a. J Pediatr Hematol Oncol. 2013 Oct;35(7):547-50. doi: 10.1097/MPH.0b013e31827e56cb. J Pediatr Hematol Oncol. 2013. PMID: 23337544
Differentiation of Fanconi anemia and aplastic anemia using mitomycin C test in Tunisia.
Talmoudi F, Kilani O, Ayed W, Ben Halim N, Mellouli F, Torjmane L, Aissaoui L, Ben Youssef Y, Kammoun L, Ben Othmane T, Bejaoui M, Ben Romdhane N, Elloumi M, Hadiji S, Hentati S, Chemkhi I, Abidli N, Guermani H, Abdelhak S, Amouri A. Talmoudi F, et al. Among authors: amouri a. C R Biol. 2013 Jan;336(1):29-33. doi: 10.1016/j.crvi.2013.02.001. Epub 2013 Mar 11. C R Biol. 2013. PMID: 23537767 Free article.
104 results