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Diagnostic challenge in a series of eleven patients with hyper IgE syndromes.
Yaakoubi R, Mekki N, Ben-Mustapha I, Ben-Khemis L, Bouaziz A, Ben Fraj I, Ammar J, Hamzaoui A, Turki H, Boussofara L, Denguezli M, Haddad S, Ouederni M, Bejaoui M, Chan KW, Lau YL, Mellouli F, Barbouche MR, Ben-Ali M. Yaakoubi R, et al. Among authors: ouederni m. Front Immunol. 2023 Jan 10;13:1057679. doi: 10.3389/fimmu.2022.1057679. eCollection 2022. Front Immunol. 2023. PMID: 36703986 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: ouederni m. J Pediatr Hematol Oncol. 2013 Oct;35(7):547-50. doi: 10.1097/MPH.0b013e31827e56cb. J Pediatr Hematol Oncol. 2013. PMID: 23337544
Budd-Chiari syndrome in a boy with β thalassemia major (a study of a new case).
Guirat-Dhouib N, Mellouli F, Abdelaali A, Ouederni M, Guedri R, Dridi Y, Askri M, Bejaoui M. Guirat-Dhouib N, et al. Among authors: ouederni m. J Pediatr Hematol Oncol. 2013 Apr;35(3):237. doi: 10.1097/MPH.0b013e3182880784. J Pediatr Hematol Oncol. 2013. PMID: 23511493 No abstract available.
Clinical features of Candidiasis in patients with inherited interleukin 12 receptor β1 deficiency.
Ouederni M, Sanal O, Ikinciogullari A, Tezcan I, Dogu F, Sologuren I, Pedraza-Sánchez S, Keser M, Tanir G, Nieuwhof C, Colino E, Kumararatne D, Levy J, Kutukculer N, Aytekin C, Herrera-Ramos E, Bhatti M, Karaca N, Barbouche R, Broides A, Goudouris E, Franco JL, Parvaneh N, Reisli I, Strickler A, Shcherbina A, Somer A, Segal A, Angel-Moreno A, Lezana-Fernandez JL, Bejaoui M, Bobadilla-Del Valle M, Kachboura S, Sentongo T, Ben-Mustapha I, Bustamante J, Picard C, Puel A, Boisson-Dupuis S, Abel L, Casanova JL, Rodríguez-Gallego C. Ouederni M, et al. Clin Infect Dis. 2014 Jan;58(2):204-13. doi: 10.1093/cid/cit722. Epub 2013 Nov 1. Clin Infect Dis. 2014. PMID: 24186907 Free PMC 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: ouederni m. 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.
Report of the Tunisian Registry of Primary Immunodeficiencies: 25-Years of Experience (1988-2012).
Mellouli F, Mustapha IB, Khaled MB, Besbes H, Ouederni M, Mekki N, Ali MB, Larguèche B, Hachicha M, Sfar T, Gueddiche N, Barsaoui S, Sammoud A, Boussetta K, Becher SB, Meherzi A, Guandoura N, Boughammoura L, Harbi A, Amri F, Bayoudh F, Jaballah NB, Tebib N, Bouaziz A, Mahfoudh A, Aloulou H, Mansour LB, Chabchoub I, Boussoffara R, Chemli J, Bouguila J, Hassayoun S, Hammami S, Habboul Z, Hamzaoui A, Ammar J, Barbouche MR, Bejaoui M. Mellouli F, et al. Among authors: ouederni m. J Clin Immunol. 2015 Nov;35(8):745-53. doi: 10.1007/s10875-015-0206-9. Epub 2015 Oct 13. J Clin Immunol. 2015. PMID: 26464197 Review.
82 results