Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Cherifa Benlatreche"'
Autor:
D.-E. Mekhancha, L. Nezzal, C.C. Dahel-Mekhancha, R. Karoune, Brahim Badaoui, Cherifa Benlatreche
Publikováno v:
Nutrition Clinique et Métabolisme. 31:125-133
Resume Objectif Evaluer la qualite de l’alimentation d’adolescents algeriens par un score d’adequation derive du Programme national nutrition Sante -Guideline Score (PNNS- GS ), dont la valeur maximale de 8 signait une adequation aux recommanda
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::687a9dbe270f05585dae7a5df1095cf7
https://doi.org/10.1016/j.nupar.2016.12.001
https://doi.org/10.1016/j.nupar.2016.12.001
Publikováno v:
Cahiers de Nutrition et de Diététique. 52:100-105
Resume La prevalence de la carence en vitamine A a ete evaluee sur 102 enfants prescolarises issus d’une population defavorisee de la ville de Constantine. Un questionnaire destine aux parents a servi a la collecte des donnees sur l’enfant. Les p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2a198e4eaf55b180b11ff4b58480e13
https://doi.org/10.1016/j.cnd.2016.10.005
https://doi.org/10.1016/j.cnd.2016.10.005
Autor:
Cherifa Benlatreche, Mohamed Habib Belmahi, Houda Sbayou, Awatif Boumaza, Fatima Khelifi Touhami, Samira Ferdi
Publikováno v:
Journal of Life Sciences. 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db231453588893e2ae9deb76ac03eedf
https://doi.org/10.17265/1934-7391/2016.04.004
https://doi.org/10.17265/1934-7391/2016.04.004
Autor:
Ouarda Semmame, Dalila Satta, Noureddine Abadi, Douadi Hamane, Mohamed Larbi Rezgoune, Cherifa Benlatreche, Djalila Chellat
Publikováno v:
Genetic Testing and Molecular Biomarkers. 16:874-878
The C677T allele of the methylenetetrahydrofolate reductase (MTHFR) gene has been suggested to represent a risk factor for male infertility. To confirm this association, the distribution of the single-nucleotide polymorphism C677T was investigated in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44f992acae6381e5947ff4b996862cfd
https://doi.org/10.1089/gtmb.2011.0367
https://doi.org/10.1089/gtmb.2011.0367
Publikováno v:
Immuno-analyse & Biologie Spécialisée. 27:122-127
Summary The common single nucleotide polymorphism (SNP) C677 T in the MTHFR gene is the first genetic risk factor of neural tube defects (NTD). It has been shown to be present, in increased frequency, in some studies in patients having neural tube de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fedfecacd70cce4523d4d276c34b7c74
https://doi.org/10.1016/j.immbio.2012.02.004
https://doi.org/10.1016/j.immbio.2012.02.004
Autor:
Zahira Houcher, Abderrezak Touabti, Bakhouche Houcher, Mounira Amrane, Rachid Malek, Samia Begag, Cherifa Benlatreche, Slimane Laouamri
Publikováno v:
Pteridines, Vol 23, Iss 1, Pp 96-103 (2012)
Homocysteine (HCY) has been identified as a risk factor for vascular disease in the general population. Diabetic retinopathy (DR) itself rather than hyperhomocysteinemia is the leading cause of blindness among patients with type 2 diabetes mellitus (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48fe0f5609e9f3d44d898fb031215aa6
https://doi.org/10.1515/pteridines.2012.23.1.96
https://doi.org/10.1515/pteridines.2012.23.1.96
Publikováno v:
Journal of Metabolic Syndrome.
Background: Obesity increases the incidence of diabetes, hypertension, dyslipidemia, atherosclerosis, and cancer. Oxidative stress has been considered one of the mechanisms linking obesity to these pathologies. Our aim was to evaluate the oxidative s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc508a0f7b37967c6e5b9731325b28f9
https://doi.org/10.4172/2167-0943.1000188
https://doi.org/10.4172/2167-0943.1000188
Publikováno v:
Annales d'Endocrinologie. 77:521-522
Introduction et objectif De nombreuses etudes soutiennent la contribution majeure du stress oxydatif dans la survenue des complications du diabete de type 2 y compris l’hypertension arterielle. L’objectif de notre etude etait de documenter la rel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c545426983d52f2d8db901e52b9166e
https://doi.org/10.1016/j.ando.2016.07.824
https://doi.org/10.1016/j.ando.2016.07.824
Autor:
Paul Valensi, A. Lezzar, Cherifa Benlatreche, Jacques Pariès, K. Benmohammed, Farah Benmohammed, M. Benlatreche, S. Khensal, M.T. Nguyen
Publikováno v:
Diabetesmetabolism. 41(2)
Objectives This study aimed to estimate, in a large group of Algerian adolescents, the prevalence of the metabolic syndrome (MetS), using four definitions (by Cook, De Ferranti, Viner and the IDF), and to test the validity of unique thresholds of wai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1c762f7b603dd3798ee8284d903b0b3
https://pubmed.ncbi.nlm.nih.gov/25108350
https://pubmed.ncbi.nlm.nih.gov/25108350
Autor:
Cherifa Benlatreche, Arnold Munnich, Jean-Paul Bonnefont, Yamina Sifi, Z. Bouderda, A. Hamri, Assia Boulefkhad, Nourredine Abadi, R. Cheriet, M. Magen, K. Sifi
Publikováno v:
Journal of Neurodegenerative Diseases
Spinal muscular atrophy (SMA) is the second most common lethal autosomal recessive disorder. It is divided into the acute Werdnig-Hoffmann disease (type I), the intermediate form (type II), the Kugelberg-Welander disease (type III), and the adult for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff2acae8cba1ff2a8841ec51c3c22b89