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Page 1
Pathologic complete response to neoadjuvant imatinib of a gastric stromal tumor with concomitant mutations in KIT: A case report and literature review.
Rekaya MB, Ksontini F, Kacem LBH, Sassi F, Harigua-Souiai E, Boujneh R, H'mayada A, Zaimi Y, Ayadi M, Trabelsi M, Mrad R, Rammeh S. Rekaya MB, et al. Among authors: trabelsi m. Clin Case Rep. 2023 Jun 7;11(6):e7463. doi: 10.1002/ccr3.7463. eCollection 2023 Jun. Clin Case Rep. 2023. PMID: 37305871 Free PMC article.
Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health.
Mkaouar R, Riahi Z, Marrakchi J, Mezzi N, Romdhane L, Boujemaa M, Dallali H, Sayeb M, Lahbib S, Jaouadi H, Boudabbous H, Zekri L, Chargui M, Messaoud O, Elyounsi M, Kraoua I, Zaouak A, Turki I, Mokni M, Boucher S, Petit C, Giraudet F, Mbarek C, Besbes G, Halayem S, Zainine R, Turki H, Tounsi A, Bonnet C, Mrad R, Abdelhak S, Trabelsi M, Charfeddine C. Mkaouar R, et al. Among authors: trabelsi m. Front Genet. 2024 Apr 22;15:1384094. doi: 10.3389/fgene.2024.1384094. eCollection 2024. Front Genet. 2024. PMID: 38711914 Free PMC article.
Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health.
Mkaouar R, Riahi Z, Marrakchi J, Mezzi N, Romdhane L, Boujemaa M, Dallali H, Sayeb M, Lahbib S, Jaouadi H, Boudabbous H, Zekri L, Chargui M, Messaoud O, Elyounsi M, Kraoua I, Zaouak A, Turki I, Mokni M, Boucher S, Petit C, Giraudet F, Mbarek C, Besbes G, Halayem S, Zainine R, Turki H, Tounsi A, Bonnet C, Mrad R, Abdelhak S, Trabelsi M, Charfeddine C. Mkaouar R, et al. Among authors: trabelsi m. Front Genet. 2024 Jun 25;15:1437233. doi: 10.3389/fgene.2024.1437233. eCollection 2024. Front Genet. 2024. PMID: 38983270 Free PMC article.
Genetic study of Alport syndrome in Tunisia.
Younsi ME, Achour A, Kraoua L, Nesrine M, Sayari T, Abderrahim E, Laabidi J, Zouaghi MK, Kharrat M, Gargah T, Trabelsi M, M'rad R. Younsi ME, et al. Among authors: m rad r, trabelsi m. Pediatr Nephrol. 2025 Jan;40(1):103-116. doi: 10.1007/s00467-024-06474-7. Epub 2024 Aug 14. Pediatr Nephrol. 2025. PMID: 39138691
Genome Tunisia Project: paving the way for precision medicine in North Africa.
Hamdi Y, Trabelsi M, Ghedira K, Boujemaa M, Ben Ayed I, Charfeddine C, Souissi A, Rejeb I, Kammoun Rebai W, Hkimi C, Neifar F, Jandoubi N, Mkaouar R, Chaouch M, Bennour A, Kamoun S, Chaker Masmoudi H, Abid N, Mezghani Khemakhem M; GTCA Consortium; Masmoudi S, Saad A, BenJemaa L, BenKahla A, Boubaker S, Mrad R, Kamoun H, Abdelhak S, Gribaa M, Belguith N, Kharrat N, Hmida D, Rebai A. Hamdi Y, et al. Among authors: trabelsi m. Genome Med. 2024 Aug 27;16(1):104. doi: 10.1186/s13073-024-01365-w. Genome Med. 2024. PMID: 39187811 Free PMC article.
Tremor Ataxia With Central Hypomyelation Phenotype Related to a Recurrent POLR3A Mutation in Six Unrelated Tunisian Families.
Kraoua I, Jamoussi M, Drissi C, Kraoua L, Drunat S, Benrhouma H, Ben Younes T, Nagi S, Abdelhak S, Boespflug Tanguy O, Youssef-Turki IB, Trabelsi M, Dorboz I. Kraoua I, et al. Among authors: trabelsi m. Mol Genet Genomic Med. 2024 Oct;12(10):e70007. doi: 10.1002/mgg3.70007. Mol Genet Genomic Med. 2024. PMID: 39436788 Free PMC article.
169 results