Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Nizar Ben Halim"'
Autor:
Nizar Ben Halim, Sana Hsouna, Khaled Lasram, Mariem Chargui, Laaroussi Khemira, Rachid Saidane, Sonia Abdelhak, Rym Kefi
Publikováno v:
Annals of Human Biology, Vol 45, Iss 1, Pp 86-97 (2018)
Background: Douiret is an isolated Berber population from South-Eastern Tunisia. The strong geographic and cultural isolation characterising this population might have contributed to remarkable endogamy and consanguinity, which were practiced for sev
Externí odkaz:
https://doaj.org/article/9f7bc6ec21a344659691ecd2c9cb1ae8
Autor:
Soukaina Abdelwahed, Hanen Cherif, Bilel Bejaoui, Ilhem Saadouli, Tarek Hajji, Nizar Ben Halim, Awatef Ouertani, Imen Ouzari, Ameur Cherif, Wissem Mnif, Amor Mosbah, Ahmed Slaheddine Masmoudi
Publikováno v:
Main Group Chemistry. 22:143-154
The detection and quantification of Indole -3 Acetic Acid (IAA) produced by Plant growth promoting rhizobacteria (PGPR) rely on a standard well-documented assay, which remains time-consuming, laborious, and costly. These drawbacks led to sway interes
Autor:
Sana Hsouna, Rachid Saidane, Sonia Abdelhak, Laaroussi Khemira, Khaled Lasram, Nizar Ben Halim, Mariem Chargui, Rym Kefi
Publikováno v:
Annals of Human Biology
Annals of Human Biology, Taylor & Francis, 2018, 45 (1), pp.86--97. ⟨10.1080/03014460.2017.1414875⟩
Annals of Human Biology, Taylor & Francis, 2018, 45 (1), pp.86--97. ⟨10.1080/03014460.2017.1414875⟩
International audience; BACKGROUND Douiret is an isolated Berber population from South-Eastern Tunisia. The strong geographic and cultural isolation characterising this population might have contributed to remarkable endogamy and consanguinity, which
Autor:
Nizar Ben Halim, Habiba Ben Romdhane, Zinet Turki, Om Kalthoum Sallem, Insaf Rejeb, Abdelmajid Abid, Mariem Chargui, Majdi Nagara, Sahar Elouej, Dalenda Triki, Sonia Bahri, Henda Jamoussi, Sonia Abdelhak, Khaled Lasram, Redha Attaoua, Claude Ben Slama, Sana Hsouna, Ines Kamoun, Florin Grigorescu, Hanen Belfki-Benali, Rym Kefi
Publikováno v:
Journal of Diabetes and its Complications
Journal of Diabetes and its Complications, Elsevier, 2016, 30 (2), pp.206-211. ⟨10.1016/j.jdiacomp.2015.11.013⟩
Journal of Diabetes and its Complications, Elsevier, 2016, 30 (2), pp.206-211. ⟨10.1016/j.jdiacomp.2015.11.013⟩
International audience; Aims: Variants in the fat mass and obesity-associated gene (FTO) are associated with obesity and type 2 diabetes. However, the association of FTO variants in the MENA (Middle East and North Africa) region with MetS is largely
Autor:
Ahmed Rebai, Sonia Abdelhak, Imen Dorboz, Majdi Nagara, Lilia Romdhane, Najoua Miladi, Najla Kharrat, Odile Boespflug-Tanguy, Nizar Ben Halim, Nissaf Ben Alaya-Bouafif, Eleonore Eymard-Pierre, Rym Kefi
Publikováno v:
Neurological Sciences
Neurological Sciences, Springer Verlag, 2016, 37 (3), pp.403-409. ⟨10.1007/s10072-015-2417-5⟩
Neurological Sciences, 2016, 37 (3), pp.403-409. ⟨10.1007/s10072-015-2417-5⟩
Neurological Sciences, Springer Verlag, 2016, 37 (3), pp.403-409. ⟨10.1007/s10072-015-2417-5⟩
Neurological Sciences, 2016, 37 (3), pp.403-409. ⟨10.1007/s10072-015-2417-5⟩
International audience; Arylsulfatase A (ASA) is a lysosomal enzyme involved in the catabolism of cerebroside sulfate. ASA deficiency is associated with metachromatic leukodystrophy (MLD). Low ASA activities have also been reported in a more common c
Autor:
Slim Ben Ammar, Laroussi Khemira, Rachid Saidane, Hela Azaiez, Lilia Romdhane, Dominique Weil, Nizar Ben Halim, Sana Hsouna, Sonia Abdelhak, Christine Petit, Rym Kefi, Ghazi Besbes, Béatrice Regnault, Majdi Nagara, Khaled Lasram
Publikováno v:
Annals of Human Genetics. 79:402-417
Runs of homozygosity (ROHs) are extended genomic regions of homozygous genotypes that record populations' mating patterns in the past. We performed microarray genotyping on 15 individuals from a small isolated Tunisian community. We estimated the ind
Autor:
Slim Ben Ammar, Neji Tebib, Farah Ouechtati, Khaled Lasram, Marie Françoise Ben Dridi, Faten Talmoudi, Rym Kefi, Houyem Ouragini, Nizar Ben Halim, Insaf Rejeb, Olfa Messaoud, Asma Walha, Yosra Bouyacoub, Sonia Abdelhak, Mourad Mokni, Ahlem Amouri, Habib Messai, Sana Hsouna, Majdi Nagara, Ahlem Sabrine Ben Brick, Wafa Cherif, Leila El Matri, Faten Ben Rhouma, I. Chouchene, Mariem Ben Rekaya
Publikováno v:
American Journal of Human Biology. 28:171-180
Objectives Consanguinity is common in Tunisia. However, little information exists on its impact on recessive disorders. In this study, we evaluate the impact of consanguineous marriages on the occurrence of some specific autosomal recessive disorders
Autor:
Nizar Ben Halim, Slim Ben Ammar, Sonia Bahri, Rym Kefi, Khaled Lasram, Sana Hsouna, Abdelmajid Abid, Sonia Abdelhak, Imen Arfa, Sounnia Mediene-Benchekor, Soraya Benhamamouch, Houda Benrahma, Henda Jamoussi, Abdelhamid Barakat
Publikováno v:
Journal of Diabetes. 7:102-113
Background The insulin-like growth factor 2 mRNA-binding protein 2 (IGF2BP2) and the cyclin-dependent kinase 5 regulatory subunit-associated protein 1-like 1 (CDKAL1) identified through genome-wide association (GWA) studies have been shown to be asso
Autor:
Crystel Bonnet, Mariem Ben Rekaya, Nizar Ben Halim, Yosra Bouyacoub, Giovanni Romeo, Insaf Rejeb, Olfa Messaoud, Faten Ben Rhouma, Lilia Romdhane, Christine Petit, Habib Messai, Zied Riahi, Sonia Abdelhak, Rym Kefi, Majdi Nagara, Ken McElreavey
Publikováno v:
Human Heredity
Human Heredity, Karger, 2014, 77 (1-4), pp.167-74. ⟨10.1159/000362167⟩
Human Heredity, 2014, 77 (1-4), pp.167-74. ⟨10.1159/000362167⟩
Human Heredity, Karger, 2014, 77 (1-4), pp.167-74. ⟨10.1159/000362167⟩
Human Heredity, 2014, 77 (1-4), pp.167-74. ⟨10.1159/000362167⟩
International audience; Located at the cross-road between Europe and Africa, Tunisia is a North African country of 11 million inhabitants. Throughout its history, it has been invaded by different ethnic groups. These historical events, and consanguin
Autor:
Sonia Bahri, Nizar Ben Halim, Abdelmajid Abid, Sonia Abdelhak, Sana Hsouna, Najoua Miladi, Imen Arfa, Rym Kefi, Khaled Lasram, Henda Jamoussi, Slim Ben Ammar
Publikováno v:
Mitochondrial DNA
Mitochondrial DNA, 2015, 26 (3), pp.367-372. ⟨10.3109/19401736.2013.836508⟩
Mitochondrial DNA, 2015, 26 (3), pp.367-372. ⟨10.3109/19401736.2013.836508⟩
International audience; Mitochondrial DNA (mtDNA) variation may play an important role in the pathogenesis of type 2 diabetes (T2Ds). In this study, we aimed to explore whether mtDNA variants contribute to the susceptibility to T2Ds in a Tunisian pop