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Page 1
Association of apolipoprotein A5 gene variants with metabolic syndrome in Tunisian population.
Kefi R, Hechmi M, Dallali H, Elouej S, Jmel H, Halima YB, Nagara M, Chargui M, Fadhel SB, Romdhane S, Kamoun I, Turki Z, Abid A, Bahri S, Bahlous A, Gomis R, Baraket A, Grigorescu F, Normand C, Jamoussi H, Abdelhak S. Kefi R, et al. Among authors: chargui m. Ann Endocrinol (Paris). 2017 Jul;78(3):146-155. doi: 10.1016/j.ando.2017.01.005. Epub 2017 Jun 16. Ann Endocrinol (Paris). 2017. PMID: 28624160
Association of genetic variants in the FTO gene with metabolic syndrome: A case-control study in the Tunisian population.
Elouej S, Nagara M, Attaoua R, Sallem OK, Rejeb I, Hsouna S, Lasram K, Halim NB, Chargui M, Jamoussi H, Turki Z, Kamoun I, Belfki-Benali H, Abid A, Slama CB, Bahri S, Triki D, Romdhane HB, Abdelhak S, Kefi R, Grigorescu F. Elouej S, et al. Among authors: chargui m. J Diabetes Complications. 2016 Mar;30(2):206-11. doi: 10.1016/j.jdiacomp.2015.11.013. Epub 2015 Nov 14. J Diabetes Complications. 2016. PMID: 26700404
Association of rs9939609 Polymorphism with Metabolic Parameters and FTO Risk Haplotype Among Tunisian Metabolic Syndrome.
Elouej S, Belfki-Benali H, Nagara M, Lasram K, Attaoua R, Sallem OK, Kamoun I, Chargui M, Romdhane L, Jamoussi H, Turki Z, Abid A, Ben Slama C, Bahri S, Abdelhak S, Grigorescu F, Ben Romdhane H, Kefi R. Elouej S, et al. Among authors: chargui m. Metab Syndr Relat Disord. 2016 Mar;14(2):121-8. doi: 10.1089/met.2015.0090. Epub 2016 Jan 7. Metab Syndr Relat Disord. 2016. PMID: 26741700
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: chargui m. Acta Diabetol. 2019 May;56(5):515-523. doi: 10.1007/s00592-018-01283-5. Epub 2019 Jan 17. Acta Diabetol. 2019. PMID: 30656436
Whole Exome Sequencing allows the identification of two novel groups of Xeroderma pigmentosum in Tunisia, XP-D and XP-E: Impact on molecular diagnosis.
Ben Rekaya M, Naouali C, Messaoud O, Jones M, Bouyacoub Y, Nagara M, Pippucci T, Jmel H, Chargui M, Jerbi M, Alibi M, Dallali H, Bashamboo A, McElreavey K, Romeo G, Barakat A, Zghal M, Yacoub-Youssef H, Abdelhak S. Ben Rekaya M, et al. Among authors: chargui m. J Dermatol Sci. 2018 Feb;89(2):172-180. doi: 10.1016/j.jdermsci.2017.10.015. Epub 2017 Nov 2. J Dermatol Sci. 2018. PMID: 29169765
Family specific genetic predisposition to breast cancer: results from Tunisian whole exome sequenced breast cancer cases.
Hamdi Y, Boujemaa M, Ben Rekaya M, Ben Hamda C, Mighri N, El Benna H, Mejri N, Labidi S, Daoud N, Naouali C, Messaoud O, Chargui M, Ghedira K, Boubaker MS, Mrad R, Boussen H, Abdelhak S; PEC Consortium. Hamdi Y, et al. Among authors: chargui m. J Transl Med. 2018 Jun 7;16(1):158. doi: 10.1186/s12967-018-1504-9. J Transl Med. 2018. PMID: 29879995 Free PMC article.
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: chargui m. 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.
A founder large deletion mutation in Xeroderma pigmentosum-Variant form in Tunisia: implication for molecular diagnosis and therapy.
Ben Rekaya M, Laroussi N, Messaoud O, Jones M, Jerbi M, Naouali C, Bouyacoub Y, Chargui M, Kefi R, Fazaa B, Boubaker MS, Boussen H, Mokni M, Abdelhak S, Zghal M, Khaled A, Yacoub-Youssef H. Ben Rekaya M, et al. Among authors: chargui m. Biomed Res Int. 2014;2014:256245. doi: 10.1155/2014/256245. Epub 2014 May 4. Biomed Res Int. 2014. PMID: 24877075 Free PMC article. Clinical Trial.
26 results