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Clinical Laboratory|September 23, 2010
Absence of anti-pendrin auto-antibodies in the sera of Tunisian patients with autoimmune thyroid diseasesSalima Belguith-Maalej, Hassen Hadj-Kacem, Sandra A Rebuffat, et al.European Cytokine Network|October 30, 2007
Association analysis of interleukin gene polymorphisms in autoimmune thyroid diseases in the Tunisian populationMaha Kammoun-Krichen, Noura Bougacha-Elleuch, Kaouthar Makni, et al.Immunobiology|November 2, 2010
SLC26A4 expression among autoimmune thyroid tissuesSalima Belguith-Maalej, Sandra A Rebuffat, Ilhem Charfeddine, et al.Journal of Diabetes and Its Complications|July 17, 2016
Whole mitochondrial genome screening of a family with maternally inherited diabetes and deafness (MIDD) associated with retinopathy: A putative haplotype associated to MIDD and a novel MT-CO2 m.8241T>G mutationMouna Tabebi, Nadia Charfi, Fakhri Kallabi, et al.Metabolic Syndrome and Related Disorders|January 17, 2024
Metabolic Disorders During ProlactinomasMouna Elleuch, Molka Ben Bnina, Fatma Loukil, et al.La Tunisie Medicale|April 8, 2026
Prevalence and predictors of self-care practices among diabetic patients in Southern TunisiaDhoha Ben Salah, Nouha Ketata, Eya Ketata, et al.Journal of Cellular and Molecular Medicine|January 6, 2026
First LDLRAP1 and Recurrent LDLR Mutations in Tunisian Families With Familial HypercholesterolemiaWirath Ben Ncir, Afif Ben-Mahmoud, Hamdi Frikha, et al.Cancer Biomarkers : Section a of Disease Markers|September 8, 2011
Genetic investigation of FOXE1 polyalanine tract in thyroid diseases: new insight on the role of FOXE1 in thyroid carcinomaRihab Kallel, Salima Belguith-Maalej, Abdelmounaim Akdi, et al.Nutrition & Diabetes|May 26, 2018
Affinity kinetics of leptin-reactive immunoglobulins are associated with plasma leptin and markers of obesity and diabetesHouda Bouhajja, Noura Bougacha-Elleuch, Nicolas Lucas, et al.Biochemical and Biophysical Research Communications|February 22, 2015
A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with severe nephropathyMouna Tabebi, Emna Mkaouar-Rebai, Mouna Mnif, et al.Pageof 7