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Page 1
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: aissaoui l. J Pediatr Hematol Oncol. 2013 Oct;35(7):547-50. doi: 10.1097/MPH.0b013e31827e56cb. J Pediatr Hematol Oncol. 2013. PMID: 23337544
Fanconi anemia: contribution of molecular analyses to the identification of bone marrow graft donors and the study of chimerism in grafted patients.
Bouchlaka C, Othman TB, Aissaoui L, Elloumi H, Elloumi M, Amouri A, Abid HB, Hadiji S, Slama H, Makni H, Saad A, Abdelhak S, Dellagi K; Tunisian Fanconi Anemia Study Group. Bouchlaka C, et al. Among authors: aissaoui l. Genet Test. 2004 Fall;8(3):268-75. doi: 10.1089/gte.2004.8.268. Genet Test. 2004. PMID: 15727250
Single autologous stem-cell transplantation followed by maintenance therapy with thalidomide is superior to double autologous transplantation in multiple myeloma: results of a multicenter randomized clinical trial.
Abdelkefi A, Ladeb S, Torjman L, Othman TB, Lakhal A, Romdhane NB, Omri HE, Elloumi M, Belaaj H, Jeddi R, Aissaouï L, Ksouri H, Hassen AB, Msadek F, Saad A, Hsaïri M, Boukef K, Amouri A, Louzir H, Dellagi K, Abdeladhim AB; Tunisian Multiple Myeloma Study Group. Abdelkefi A, et al. Among authors: aissaoui l. Blood. 2008 Feb 15;111(4):1805-10. doi: 10.1182/blood-2007-07-101212. Epub 2007 Sep 17. Blood. 2008. Retraction in: Blood. 2009 Jun 11;113(24):6265. doi: 10.1182/blood-2009-05-222927 PMID: 17875806 Free article. Retracted. Clinical Trial.
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: aissaoui l. 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.
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. Among authors: aissaoui l. 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.
Homozygous transcription factor 3 gene (TCF3) mutation is associated with severe hypogammaglobulinemia and B-cell acute lymphoblastic leukemia.
Ben-Ali M, Yang J, Chan KW, Ben-Mustapha I, Mekki N, Benabdesselem C, Mellouli F, Bejaoui M, Yang W, Aissaoui L, Lau YL, Barbouche MR. Ben-Ali M, et al. Among authors: aissaoui l. J Allergy Clin Immunol. 2017 Oct;140(4):1191-1194.e4. doi: 10.1016/j.jaci.2017.04.037. Epub 2017 May 19. J Allergy Clin Immunol. 2017. PMID: 28532655 No abstract available.
[Hemoglobin C disease: report of 16 Tunisian cases].
Hafsia R, Marrakchi O, Ben Salah N, Gouider E, Ben Lakhal R, Jeddi R, Aissaoui L, Belhadjali Z, Ben Abid H, Meddeb B, Hafsia A. Hafsia R, et al. Among authors: aissaoui l. Tunis Med. 2007 Mar;85(3):209-11. Tunis Med. 2007. PMID: 17668575 French.
Treatment of acute promyelocytic leukemia with PETHEMA LPA 99 protocol: a Tunisian single center experience.
Jeddi R, Ghédira H, Menif S, Ben Neji H, Ben Amor R, Kacem K, Aissaoui L, Bouteraâ W, Abdennebi Y, Raihane BL, Gouider E, Raouf H, Hèla BA, Saad A, Zaher B, Meddeb B. Jeddi R, et al. Among authors: aissaoui l. Hematology. 2010 Aug;15(4):204-9. doi: 10.1179/102453309X12583347114176. Hematology. 2010. PMID: 20670478 Free article. Clinical Trial.
33 results