Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Hajer Siala"'
Autor:
I. Bel Hadj, K. Bousetta, Rym Dabboubi, Hajer Siala, Chaima Abdelhafidh Sahli, S. Hadj Fredj, Taieb Messaoud, Imen Wahabi
Publikováno v:
Revue Française d'Allergologie. 59:363-368
Objective Asthma is a multifactorial disease of genetic origin; its clinical expression depends largely on acquired factors, often related to the environment. It is defined as a chronic inflammatory condition of the airways with mucus obstruction, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4445b5884e18cdae7396e435245a1cf4
https://doi.org/10.1016/j.reval.2019.05.001
https://doi.org/10.1016/j.reval.2019.05.001
Autor:
F. Khalsi, Malek Nefzi, Khedija Bousetta, Hajer Siala, Sondess Hadj Fredj, Imen Wahabi, Rym Dabboubi, Taieb Messaoud
Publikováno v:
Allergologia et Immunopathologia. 47:159-165
Introduction and Objectives Asthma is a complex genetic disorder. Several genes have been found associated with asthma. The cystic fibrosis transmembrane conductance regulator (CFTR) gene is one of them. The aim of this study was to perform a compara
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d310d45b25dcf574bb68bc18f4b14d31
https://doi.org/10.1016/j.aller.2018.06.007
https://doi.org/10.1016/j.aller.2018.06.007
Autor:
Latifa Jouini, Sabrine Haloui, Amina Bibi, Chaima Abdelhafidh Sahli, Rym Daboubi, Nourelhouda Toumi, Taieb Messsaoud, Naouel Laouini, Hajer Siala, Faida Ouali, Sondes Hadj Fredj, Meriam Becher
Publikováno v:
Clinical Chemistry and Laboratory Medicine (CCLM). 55:1193-1201
Background:Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the commonest enzymopathy worldwide. The incidence depends essentially on the methods used for the assessment. In this respect, we attempted in this study to set cut-off values of G6PD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a06dc9f969865e6dd7b83f63300d59dc
https://doi.org/10.1515/cclm-2016-0253
https://doi.org/10.1515/cclm-2016-0253
Autor:
Chaïma Abdelhafidh Sahli, Taieb Messaoud, Maroua Hammami, Rim Daboubi, Maha Ben Sedrine, Rahma Mahjoub, Radhouene Doggui, Hajer Siala, Wassef Lotfi Aissa, Amina Bibi, Khemais Zouaoui
Publikováno v:
ELECTROPHORESIS. 38:2210-2218
HbA1c is used for monitoring diabetic balance. In this paper we report an assessment of the analytical performances of Capillarys 2 Flex Piercing (C2FP) for HbA1c measurement using CE (Capillary Electrophoresis). CLSI (Clinical and Laboratory Standar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17e4e889a385418a9f4f23b7acb812b8
https://doi.org/10.1002/elps.201600423
https://doi.org/10.1002/elps.201600423
Publikováno v:
Sport Sciences for Health. 12:233-238
The present study attempted to test whether the angiotensin-converting enzyme (ACE) genotypes can be associated with precompetitive anxiety that can be potentially used as predictors of athletic performance. Eighty-seven track and field athletes (47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6da1049e2bbc1baeeb02e5ef037aee76
https://doi.org/10.1007/s11332-016-0280-2
https://doi.org/10.1007/s11332-016-0280-2
Autor:
Naouel Laouini, Taieb Messaoud, Rym Dabboubi, B. Dakhlaoui, Rym Othmeni, Latifa Jouini, Fattoum S, Hajer Siala, Sondes Hadj Fredj, Ikbel Ben Salem, Amina Bibi, Chaima Abdelhafidh Sahli
Publikováno v:
Journal of Clinical Laboratory Analysis. 30:392-398
Backgrounds β-Thalassemia is one of the most prevalent worldwide autosomal recessive disorders. It presents a great molecular heterogeneity resulting from more than 200 causative mutations in the β-globin gene. In Tunisia, β-thalassemia represents
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f566c3c685e459dfedcdcdc4cf737f87
https://doi.org/10.1002/jcla.21867
https://doi.org/10.1002/jcla.21867
Publikováno v:
Clinica Chimica Acta. 493:S238-S239
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c95fafcc463aea78ae928c9b4c10409f
https://doi.org/10.1016/j.cca.2019.03.493
https://doi.org/10.1016/j.cca.2019.03.493
Autor:
Aroua Cherif, Samir Belal, Nadia Ben Ali, Nadia Anane, Saloua Fray, Sondes Hadj-Fredj, Mariem Kechaou, Nouria Oudiaa Zakraoui, Slim Echebi, Afef Achouri-Rassas, Taieb Messaoud, Hajer Siala
Publikováno v:
Journal of Neural Transmission. 123:317-321
Angiotensin-converting enzyme (ACE) has shown altered activity in patients with neurological diseases. An insertion/deletion (I/D) polymorphism of the ACE gene encoding angiotensin-converting enzyme has been reported to be associated with the risk fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edbdfd1a34473dda3effe82fbbd822cd
https://doi.org/10.1007/s00702-015-1468-3
https://doi.org/10.1007/s00702-015-1468-3
Autor:
Neji Tebib, Malek Nefzi, Sihem Barsaoui, Hajer Siala, S. Hadj Fredj, K. Boussetta, Taieb Messaoud
Publikováno v:
Pathologie Biologie. 63:169-174
Purpose Determining the frequency of M470V polymorphism in cystic fibrosis and healthy cohort in Tunisia to establish the contribution of M470V polymorphism in cystic fibrosis variable presentation and course. Additionally, studying the origin of cys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdb8731c2a4943b2249a855cb82ddd71
https://doi.org/10.1016/j.patbio.2015.07.004
https://doi.org/10.1016/j.patbio.2015.07.004
Autor:
Rym Dabboubi, Souheil Omar, Naziha Kaabachi, Sami Gritli, Hajer Siala, Chaima Abdelhafidh Sahli, Amina Bibi, Taieb Messaoud
Publikováno v:
Annales de biologie clinique. 73:353-358
The most common inherited haemoglobin disorders encountered in Tunisia are β-thalassemia and sickle cell disease, which result from mutations in the β-globin gene. Few studies focused on δ-globin gene variations responsible for δ-thalassemia or H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3cb8f1c6a46059080e81cd52aafee12
https://doi.org/10.1684/abc.2015.1040
https://doi.org/10.1684/abc.2015.1040