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La Tunisie Medicale|March 28, 2024
The effect of therapeutic education program on quality of life among type 2 diabetic North-African patients: a randomized controlled trialImen Turki, Mouna Mnif, Chekib ZediniIndian Journal of Endocrinology and Metabolism|November 20, 2013
Congenital adrenal hyperplasia: Treatment and outcomesMahdi Kamoun, Mouna Mnif Feki, Mohamed Habib Sfar, et al.Genetics Research|March 5, 2013
Association of intronic repetition of SLC26A4 gene with Hashimoto thyroiditis diseaseSalima Belguith-Maalej, Rihab Kallel, Mouna Mnif, et al.Immunobiology|July 29, 2008
Thyroglobulin polymorphisms in Tunisian patients with autoimmune thyroid diseases (AITD)Salima Belguith-Maalej, Hassen Hadj Kacem, Ahmed Rebai, et al.Annals of Human Biology|November 8, 2008
TNF gene polymorphisms in Graves' disease: TNF-308 A/G meta-analysisMaha Kammoun-Krichen, Noura Bougacha-Elleuch, Ahmed Rebai, et al.Biochemical and Biophysical Research Communications|January 30, 2013
A maternally inherited diabetes and deafness patient with the 12S rRNA m.1555A>G and the ND1 m.3308T>C mutations associated with multiple mitochondrial deletionsNajla Mezghani, Mouna Mnif, Emna Mkaouar-Rebai, et al.The Pan African Medical Journal|November 26, 2019
[Insulinoma associated with adrenocorticotropic insufficiency and hypergonadotropic hypogonadism: a case study]Faten Hadjkacem, Mahdi Kalthoum, Dorra Ghorbel, et al.Gene|April 9, 2017
Intronic variants of SLC26A4 gene enhance splicing efficiency in hybrid minigene assayRihab Kallel-Bouattour, Salima Belguith-Maalej, Emna Zouari-Bradai, et al.Human Fertility (Cambridge, England)|April 15, 2020
Diagnostic value of miR-199a and miR-21 in the plasma of infertile women with dysregulated AMH levelsImen Belguith, Dhoha Dhieb, Mouna Turki, et al.Journal of Diabetes and Its Complications|January 5, 2010
The heteroplasmic m.14709T>C mutation in the tRNA(Glu) gene in two Tunisian families with mitochondrial diabetesNajla Mezghani, Emna Mkaouar-Rebai, Mouna Mnif, et al.Pageof 7