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Mitochondrial DNA sequence diversity in a sedentary population from Egypt.
Stevanovitch A, Gilles A, Bouzaid E, Kefi R, Paris F, Gayraud RP, Spadoni JL, El-Chenawi F, Béraud-Colomb E. Stevanovitch A, et al. Among authors: Kefi R. Ann Hum Genet. 2004 Jan;68(Pt 1):23-39. doi: 10.1046/j.1529-8817.2003.00057.x. Ann Hum Genet. 2004. PMID: 14748828
A review of clinical pharmacogenetics Studies in African populations.
Radouani F, Zass L, Hamdi Y, Rocha JD, Sallam R, Abdelhak S, Ahmed S, Azzouzi M, Benamri I, Benkahla A, Bouhaouala-Zahar B, Chaouch M, Jmel H, Kefi R, Ksouri A, Kumuthini J, Masilela P, Masimirembwa C, Othman H, Panji S, Romdhane L, Samtal C, Sibira R, Ghedira K, Fadlelmola F, Kassim SK, Mulder N. Radouani F, et al. Among authors: Kefi R. Per Med. 2020 Mar;17(2):155-170. doi: 10.2217/pme-2019-0110. Epub 2020 Mar 3. Per Med. 2020. PMID: 32125935 Free article.
Gut microbiota imbalances in Tunisian participants with type 1 and type 2 diabetes mellitus.
Fassatoui M, Lopez-Siles M, Díaz-Rizzolo DA, Jmel H, Naouali C, Abdessalem G, Chikhaoui A, Nadal B, Jamoussi H, Abid A, Gomis R, Abdelhak S, Martinez-Medina M, Kefi R. Fassatoui M, et al. Among authors: Kefi R. Biosci Rep. 2019 Jun 18;39(6):BSR20182348. doi: 10.1042/BSR20182348. Print 2019 Jun 28. Biosci Rep. 2019. PMID: 31147456 Free PMC article.
Novel MED12 variant in a multiplex Fragile X syndrome family: dual molecular etiology of two X-linked intellectual disabilities with autism in the same family.
Lahbib S, Trabelsi M, Dallali H, Sakka R, Bourourou R, Kefi R, Mrad R, Abdelhak S, Gaddour N. Lahbib S, et al. Among authors: Kefi R. Mol Biol Rep. 2019 Aug;46(4):4185-4193. doi: 10.1007/s11033-019-04869-6. Epub 2019 May 16. Mol Biol Rep. 2019. PMID: 31098807
Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing.
Dallali H, Pezzilli S, Hechmi M, Sallem OK, Elouej S, Jmel H, Ben Halima Y, Chargui M, Gharbi M, Mercuri L, Alberico F, Mazza T, Bahlous A, Ben Ahmed M, Jamoussi H, Abid A, Trischitta V, Abdelhak S, Prudente S, Kefi R. Dallali H, et al. Among authors: Kefi R. Acta Diabetol. 2019 May;56(5):515-523. doi: 10.1007/s00592-018-01283-5. Epub 2019 Jan 17. Acta Diabetol. 2019. PMID: 30656436
Thiamine responsive megaloblastic anemia mimicking mitochondrial disorders.
Tinsa F, Hechmi M, Hadj IB, Khalsi F, Chargui M, Kefi R, Azouz H, Boussetta K, Abdelhak S. Tinsa F, et al. Among authors: Kefi R. Rev Neurol (Paris). 2019 May;175(5):324-327. doi: 10.1016/j.neurol.2018.07.008. Epub 2019 Jan 3. Rev Neurol (Paris). 2019. PMID: 30612703 No abstract available.
Genetic Analysis of TREM2 Variants in Tunisian Patients with Alzheimer's Disease.
Landoulsi Z, Ben Djebara M, Kacem I, Sidhom Y, Kefi R, Abdelhak S, Gargouri-Berrechid A, Gouider R. Landoulsi Z, et al. Among authors: Kefi R. Med Princ Pract. 2018;27(4):317-322. doi: 10.1159/000489779. Epub 2018 May 3. Med Princ Pract. 2018. PMID: 29723869 Free PMC article.
Pharmacogenetic landscape of Metabolic Syndrome components drug response in Tunisia and comparison with worldwide populations.
Jmel H, Romdhane L, Ben Halima Y, Hechmi M, Naouali C, Dallali H, Hamdi Y, Shan J, Abid A, Jamoussi H, Trabelsi S, Chouchane L, Luiselli D, Abdelhak S, Kefi R. Jmel H, et al. Among authors: Kefi R. PLoS One. 2018 Apr 13;13(4):e0194842. doi: 10.1371/journal.pone.0194842. eCollection 2018. PLoS One. 2018. PMID: 29652911 Free PMC article.
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