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Ovarian Steroid Cell Tumor (Not Otherwise Specified): A Case Report of Ovarian Hyperandrogenism.
Published in:
Case Reports in Oncological Medicine, 2020, p. 1, doi. 10.1155/2020/6970823
By:
- Faten, Hadjkacem;
- Dorra, Ghorbel;
- Slim, Charfi;
- Wajdi, Safi;
- Nadia, Charfi;
- Kais, Chaabene;
- Tahia, Boudawara;
- Mohamed, Abid
Publication type:
Article
The first concurrent detection of mitochondrial DNA m.3243A>G mutation, deletion, and depletion in a family with mitochondrial diabetes.
Published in:
Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 7, p. 1, doi. 10.1002/mgg3.1292
By:
- Tabebi, Mouna;
- Safi, Wajdi;
- Felhi, Rahma;
- Alila Fersi, Olfa;
- Keskes, Leila;
- Abid, Mohamed;
- Mnif, Mouna;
- Fakhfakh, Faiza
Publication type:
Article
Analysis of ProP1 Gene in a Cohort of Tunisian Patients with Congenital Combined Pituitary Hormone Deficiency.
Published in:
Journal of Clinical Medicine, 2022, v. 11, n. 24, p. 7525, doi. 10.3390/jcm11247525
By:
- Moalla, Mariam;
- Mnif-Feki, Mouna;
- Safi, Wajdi;
- Charfi, Nadia;
- Mejdoub-Rekik, Nabila;
- Abid, Mohamed;
- Hadj Kacem, Faten;
- Hadj Kacem, Hassen
Publication type:
Article
Tunisian Maturity-Onset Diabetes of the Young: A Short Review and a New Molecular and Clinical Investigation.
Published in:
Frontiers in Endocrinology, 2021, v. 12, p. 1, doi. 10.3389/fendo.2021.684018
By:
- Moalla, Mariam;
- Safi, Wajdi;
- Babiker Mansour, Maab;
- Hadj Kacem, Mohamed;
- Mahfood, Mona;
- Abid, Mohamed;
- Kammoun, Thouraya;
- Hachicha, Mongia;
- Mnif-Feki, Mouna;
- Hadj Kacem, Faten;
- Hadj Kacem, Hassen
Publication type:
Article
Potential role of liver enzyme levels as predictive markers of glucose metabolism disorders in a Tunisian population.
Published in:
Canadian Journal of Physiology & Pharmacology, 2018, v. 96, n. 11, p. 1171, doi. 10.1139/cjpp-2017-0579
By:
- Bouhajja, Houda;
- Abdelhedi, Rania;
- Amouri, Ali;
- Hadj Kacem, Faten;
- Marrakchi, Rim;
- Safi, Wajdi;
- Mrabet, Houcem;
- Chtourou, Lassaad;
- Charfi, Nadia;
- Fourati, Mouna;
- Bensassi, Salwa;
- Jamoussi, Kamel;
- Abid, Mohamed;
- Ayadi, Hammadi;
- Mnif-Feki, Mouna;
- Bougacha-Elleuch, Noura
Publication type:
Article
A novel thymidine phosphorylase mutation in a family with Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): Molecular docking, dynamic simulation and computational investigations.
Published in:
International Journal of Developmental Neuroscience, 2022, v. 82, n. 7, p. 626, doi. 10.1002/jdn.10215
By:
- Ammar, Marwa;
- Safi, Wajdi;
- Tlili, Abdelaziz;
- Alila-Fersi, Olfa;
- Frikha, Fakher;
- Chouchen, Jihen;
- Mnif, Fatma;
- Kharrat, Marwa;
- Maalej, Marwa;
- Felhi, Rahma;
- Abid, Mohamed;
- Mnif-Feki, Mouna;
- Kacem, Faten Hadj;
- Fakhfakh, Faiza;
- Mkaouar-Rebai, Emna
Publication type:
Article

Found: 6

Ovarian Steroid Cell Tumor (Not Otherwise Specified): A Case Report of Ovarian Hyperandrogenism.

The first concurrent detection of mitochondrial DNA m.3243A>G mutation, deletion, and depletion in a family with mitochondrial diabetes.

Analysis of ProP1 Gene in a Cohort of Tunisian Patients with Congenital Combined Pituitary Hormone Deficiency.

Tunisian Maturity-Onset Diabetes of the Young: A Short Review and a New Molecular and Clinical Investigation.

Potential role of liver enzyme levels as predictive markers of glucose metabolism disorders in a Tunisian population.

A novel thymidine phosphorylase mutation in a family with Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): Molecular docking, dynamic simulation and computational investigations.