Mouna Feki-Mnif
Sfax, 3029, Tunisia
Last Updated: 09/26/2026
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Found 10 publications
Analysis of ProP1 Gene in a Cohort of Tunisian Patients with Congenital Combined Pituitary Hormone Deficiency.
Journal: Journal of clinical medicine
Published: November 03, 2022
A novel thymidine phosphorylase mutation in a family with Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): Molecular docking, dynamic simulation and computational investigations.
Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience
Published: April 04, 2022
Occurrence of Hypopituitarism in Tunisian Turner Syndrome patients: familial versus sporadic cases.
Journal: Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology
Published: June 14, 2021
Tunisian Maturity-Onset Diabetes of the Young: A Short Review and a New Molecular and Clinical Investigation.
Journal: Frontiers in endocrinology
Published: March 22, 2021
Nonstop mutation in the Kisspeptin 1 receptor (KISS1R) gene causes normosmic congenital hypogonadotropic hypogonadism.
Journal: Journal of assisted reproduction and genetics
Published: February 19, 2019
Potential role of liver enzyme levels as predictive markers of glucose metabolism disorders in a Tunisian population.
Journal: Canadian journal of physiology and pharmacology
Published: March 13, 2018
Affinity kinetics of leptin-reactive immunoglobulins are associated with plasma leptin and markers of obesity and diabetes.
Journal: Nutrition & diabetes
Published: January 05, 2018
Potential Predictive Role of Lipid Peroxidation Markers for Type 2 Diabetes in the Adult Tunisian Population.
Journal: Canadian journal of diabetes
Published: April 25, 2017
Showing 1-10 of 10
Last Updated: 09/26/2026