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Wajdi Safi

Showing results (1-10 of 7) with videos related to

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La Tunisie Medicale|March 4, 2022
Simulation Based Learning in internal medicine studentsMelek Kechida, Syrine Daadaa, Wajdi Safi, et al.
Molecular Genetics & Genomic Medicine|May 13, 2020
The first concurrent detection of mitochondrial DNA m.3243A>G mutation, deletion, and depletion in a family with mitochondrial diabetesMouna Tabebi, Wajdi Safi, Rahma Felhi, et al.
Journal of Clinical Medicine|December 23, 2022
Analysis of <i>ProP1</i> Gene in a Cohort of Tunisian Patients with Congenital Combined Pituitary Hormone DeficiencyMariam Moalla, Mouna Mnif-Feki, Wajdi Safi, et al.
The Journal of Steroid Biochemistry and Molecular Biology|December 23, 2022
Molecular mechanisms underlying the defects of two novel mutations in the HSD17B3 gene found in the Tunisian populationBochra Ben Rhouma, Manuel Kley, Fakhri Kallabi, et al.
Frontiers in Endocrinology|August 16, 2021
Tunisian Maturity-Onset Diabetes of the Young: A Short Review and a New Molecular and Clinical InvestigationMariam Moalla, Wajdi Safi, Maab Babiker Mansour, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|July 15, 2022
A novel thymidine phosphorylase mutation in a family with Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): Molecular docking, dynamic simulation and computational investigationsMarwa Ammar, Wajdi Safi, Abdelaziz Tlili, et al.
Canadian Journal of Physiology and Pharmacology|March 13, 2018
Potential role of liver enzyme levels as predictive markers of glucose metabolism disorders in a Tunisian populationHouda Bouhajja, Rania Abdelhedi, Ali Amouri, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
La Tunisie Medicale|March 4, 2022
Simulation Based Learning in internal medicine studentsMelek Kechida, Syrine Daadaa, Wajdi Safi, et al.
Molecular Genetics & Genomic Medicine|May 13, 2020
The first concurrent detection of mitochondrial DNA m.3243A>G mutation, deletion, and depletion in a family with mitochondrial diabetesMouna Tabebi, Wajdi Safi, Rahma Felhi, et al.
Journal of Clinical Medicine|December 23, 2022
Analysis of <i>ProP1</i> Gene in a Cohort of Tunisian Patients with Congenital Combined Pituitary Hormone DeficiencyMariam Moalla, Mouna Mnif-Feki, Wajdi Safi, et al.
The Journal of Steroid Biochemistry and Molecular Biology|December 23, 2022
Molecular mechanisms underlying the defects of two novel mutations in the HSD17B3 gene found in the Tunisian populationBochra Ben Rhouma, Manuel Kley, Fakhri Kallabi, et al.
Frontiers in Endocrinology|August 16, 2021
Tunisian Maturity-Onset Diabetes of the Young: A Short Review and a New Molecular and Clinical InvestigationMariam Moalla, Wajdi Safi, Maab Babiker Mansour, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|July 15, 2022
A novel thymidine phosphorylase mutation in a family with Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): Molecular docking, dynamic simulation and computational investigationsMarwa Ammar, Wajdi Safi, Abdelaziz Tlili, et al.
Canadian Journal of Physiology and Pharmacology|March 13, 2018
Potential role of liver enzyme levels as predictive markers of glucose metabolism disorders in a Tunisian populationHouda Bouhajja, Rania Abdelhedi, Ali Amouri, et al.
Pageof 1