M. Hachicha

Descriptive analyses of Turner syndrome: 49 cases in Tunisia.

N. Charfi, M. Abid, A. Bouraoui, 2010, Annales d'endocrinologie.

Autoantibodies to Zinc Transporter 8 and SLC30A8 Genotype in Type 1 Diabetes Childhood: A Pioneering Study in North Africa

R. Fakhfakh, S. Feki, H. Masmoudi, 2022, Journal of diabetes research.

Brain magnetic resonance imaging findings in adult patients with congenital adrenal hyperplasia: Increased frequency of white matter impairment and temporal lobe structures dysgenesis

N. Charfi, M. Abid, M. H. Sfar, 2013, Indian journal of endocrinology and metabolism.

A novel DNAH5 variant in a Tunisian patient with primary ciliary dyskinesia

Rahma Mani, Z. Soua, J. Bouguila, 2020, Journal of Genetics.

Long-Term Outcome of Patients With Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency

Mohamed Abid, Mahdi Kamoun, Mongia Hachicha, 2012, The American journal of the medical sciences.

Occurrence of Hypopituitarism in Tunisian Turner Syndrome patients: familial versus sporadic cases

N. Charfi, M. Abid, F. Abdelhédi, 2021, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

Unusual association of turner syndrome and hypopituitarism in a Tunisian family.

N. Charfi, M. Abid, F. Abdelhédi, 2016, Current research in translational medicine.