Mouna Mnif

Analysis of skewed X-chromosome inactivation in females with rheumatoid arthritis and autoimmune thyroid diseases

Ghazi Chabchoub, Elif Uz, Abdellatif Maalej et al. · Arthritis Research & Therapy · 2009 · 120 citations · Full text

Cytogenetics, Disease Etiology, Genetics +17

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

Mouna Mnif, Mahdi Kamoun, Fatma Mnif et al. · The American Journal of the Medical Sciences · 2012 · 47 citations

Adrenal Gland, Urology, Medicine +5

The heteroplasmic m.14709T>C mutation in the tRNAGlu gene in two Tunisian families with mitochondrial diabetes

Najla Mezghani, Emna Mkaouar‐Rebai, Mouna Mnif et al. · Journal of Diabetes and its Complications · 2010 · 34 citations

Genetic Disorder, Genetics, Trnaglu Gene +7

Genetic investigation of FOXE1 polyalanine tract in thyroid diseases: New insight on the role of FOXE1 in thyroid carcinoma

Rihab Kallel, Salima Belguith-Maalej, Abdelmounaim Akdi et al. · Cancer Biomarkers · 2011 · 30 citations

Analysis of MHC genes in a Tunisian isolate with autoimmune thyroid diseases: implication of TNF −308 gene polymorphism

Noura Bougacha‐Elleuch, Ahmed Rebaï, Mouna Mnif et al. · Journal of Autoimmunity · 2004 · 30 citations

Immunogenetics, Mhc Genes, Autoimmune Disease +13