Hassen Hadj Kacem

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 7

Top Topics

Molecular Dynamics Simulations

Top Venues

Journal of clinical medicine

Journal of assisted reproduction and genetics

International journal of molecular sciences

This page only lists publications with an associated author ORCID identifier.

Publications

Baraah Tariq Shaker, Asmaa Anwar Ismail, Rawan Salih, Hassen Hadj Kacem, Mohamed Rahmani, Ingrid Struman, Khalid Bajou
The 14-Kilodalton Human Growth Hormone Fragment a Potent Inhibitor of Angiogenesis and Tumor Metastasis. International journal of molecular sciences 24 (10) (2023)
Mariam Moalla, Mouna Mnif-Feki, Wajdi Safi, Nadia Charfi, Nabila Mejdoub-Rekik, Mohamed Abid, Faten Hadj Kacem, Hassen Hadj Kacem
Analysis of ProP1 Gene in a Cohort of Tunisian Patients with Congenital Combined Pituitary Hormone Deficiency. Journal of clinical medicine 11 (24) (2022)
Mariam Moalla, Mouna Mnif-Feki, Wajdi Safi, Nadia Charfi, Nabila Mejdoub-Rekik, Mohamed Abid, Faten Hadj Kacem, Hassen Hadj Kacem
Analysis of ProP1 Gene in a Cohort of Tunisian Patients with Congenital Combined Pituitary Hormone Deficiency. Journal of clinical medicine 11 (24) (2022)
Mariam Moalla, Mouna Mnif-Feki, Wajdi Safi, Nadia Charfi, Nabila Mejdoub-Rekik, Mohamed Abid, Faten Hadj Kacem, Hassen Hadj Kacem
Analysis of ProP1 Gene in a Cohort of Tunisian Patients with Congenital Combined Pituitary Hormone Deficiency. Journal of clinical medicine 11 (24) (2022)
Mariam Moalla, Mouna Mnif-Feki, Wajdi Safi, Nadia Charfi, Nabila Mejdoub-Rekik, Mohamed Abid, Faten Hadj Kacem, Hassen Hadj Kacem
Analysis of ProP1 Gene in a Cohort of Tunisian Patients with Congenital Combined Pituitary Hormone Deficiency. Journal of clinical medicine 11 (24) (2022)
Mariam Moalla, Mouna Mnif-Feki, Wajdi Safi, Nadia Charfi, Nabila Mejdoub-Rekik, Mohamed Abid, Faten Hadj Kacem, Hassen Hadj Kacem
Analysis of ProP1 Gene in a Cohort of Tunisian Patients with Congenital Combined Pituitary Hormone Deficiency. Journal of clinical medicine 11 (24) (2022)
Mariam Moalla, Faten Hadj Kacem, Abdullah Fahad Al-Mutery, Mona Mahfood, Nabila Mejdoub-Rekik, Mohamed Abid, Mouna Mnif-Feki, Hassen Hadj Kacem
Nonstop mutation in the Kisspeptin 1 receptor (KISS1R) gene causes normosmic congenital hypogonadotropic hypogonadism. Journal of assisted reproduction and genetics 36 (6) (2019)