| Complicated urinary tract infections associated with diabetes mellitus: Pathogenesis, diagnosis and management MF Mnif, M Kamoun, FH Kacem, Z Bouaziz, N Charfi, F Mnif, BB Naceur, ... Indian journal of endocrinology and metabolism 17 (3), 442, 2013 | 145 | 2013 |
| Analysis of skewed X-chromosome inactivation in females with rheumatoid arthritis and autoimmune thyroid diseases G Chabchoub, E Uz, A Maalej, CA Mustafa, A Rebai, M Mnif, Z Bahloul, ... Arthritis research & therapy 11, 1-8, 2009 | 121 | 2009 |
| Adrenal diseases during pregnancy: pathophysiology, diagnosis and management strategies M Kamoun, MF Mnif, N Charfi, FH Kacem, BB Naceur, F Mnif, M Dammak, ... The American journal of the medical sciences 347 (1), 64-73, 2014 | 89 | 2014 |
| Long-term outcome of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency MF Mnif, M Kamoun, F Mnif, N Charfi, N Kallel, BB Naceur, N Rekik, ... The American journal of the medical sciences 344 (5), 363-373, 2012 | 53 | 2012 |
| Analysis of MHC genes in a Tunisian isolate with autoimmune thyroid diseases: implication of TNF− 308 gene polymorphism N Bougacha-Elleuch, A Rebai, M Mnif, H Makni, M Bellassouad, J Jouida, ... Journal of autoimmunity 23 (1), 75-80, 2004 | 49 | 2004 |
| Genetic investigation of FOXE1 polyalanine tract in thyroid diseases: new insight on the role of FOXE1 in thyroid carcinoma R Kallel, S Belguith-Maalej, A Akdi, M Mnif, I Charfeddine, P Galofré, ... Cancer Biomarkers 8 (1), 43-51, 2011 | 44 | 2011 |
| The heteroplasmic m. 14709T> C mutation in the tRNAGlu gene in two Tunisian families with mitochondrial diabetes N Mezghani, E Mkaouar-Rebai, M Mnif, N Charfi, N Rekik, S Youssef, ... Journal of Diabetes and its Complications 24 (4), 270-277, 2010 | 39 | 2010 |
| Reproductive outcomes of female patients with congenital adrenal hyperplasia due to 21-hydroxylase defi ciency MF Mnif, M Kamoun, FH Kacem, F Mnif, N Charfi, BB Naceur, N Rekik, ... Indian Journal of Endocrinology and Metabolism 17 (5), 790-793, 2013 | 36 | 2013 |
| A novel mutation MT-COIII m. 9267G> C and MT-COI m. 5913G> A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD … M Tabebi, E Mkaouar-Rebai, M Mnif, F Kallabi, AB Mahmoud, WB Saad, ... Biochemical and biophysical research communications 459 (3), 353-360, 2015 | 35 | 2015 |
| Association between Leptin gene polymorphisms and plasma leptin level in three consanguineous families with obesity M Fourati, M Mnif, N Kharrat, N Charfi, M Kammoun, N Fendri, S Sessi, ... Gene 527 (1), 75-81, 2013 | 35 | 2013 |
| Management of Type 2 diabetes in Ramadan: Low-ratio premix insulin working group practical advice M Hassanein, M Belhadj, K Abdallah, AD Bhattacharya, AK Singh, ... Indian journal of endocrinology and metabolism 18 (6), 794, 2014 | 32 | 2014 |
| A maternally inherited diabetes and deafness patient with the 12S rRNA m. 1555A> G and the ND1 m. 3308T> C mutations associated with multiple mitochondrial deletions N Mezghani, M Mnif, E Mkaouar-Rebai, N Kallel, N Charfi, M Abid, ... Biochemical and Biophysical Research Communications 431 (4), 670-674, 2013 | 31 | 2013 |
| Brain magnetic resonance imaging findings in adult patients with congenital adrenal hyperplasia: increased frequency of white matter impairment and temporal lobe structures … MF Mnif, M Kamoun, F Mnif, N Charfi, N Kallel, N Rekik, BB Naceur, ... Indian journal of endocrinology and metabolism 17 (1), 121-127, 2013 | 30 | 2013 |
| Mutational analysis of the mitochondrial tRNALeu (UUR) gene in Tunisian patients with mitochondrial diseases E Mkaouar-Rebai, A Tlili, S Masmoudi, N Belguith, I Charfeddine, M Mnif, ... Biochemical and Biophysical Research Communications 355 (4), 1031-1037, 2007 | 29 | 2007 |
| Thyroid hypoplasia in congenital hypothyroidism associated with thyroid peroxidase mutations A Stoupa, R Chaabane, M Guériouz, C Raynaud-Ravni, P Nitschke, ... Thyroid 28 (7), 941-944, 2018 | 28 | 2018 |
| Hyperparathyroidism-jaw tumor syndrome: a case report N Rekik, BB Naceur, M Mnif, F Mnif, H Mnif, T Boudawara, M Abid Annales d'endocrinologie 71 (2), 121-126, 2010 | 28 | 2010 |
| Ganglioneuroma of adrenal gland in a patient with Turner syndrome M Kamoun, MF Mnif, N Rekik, N Belguith, N Charfi, L Mnif, M Elleuch, ... Annals of diagnostic pathology 14 (2), 133-136, 2010 | 27 | 2010 |
| Effect of exercise training intensity on body composition, lipid profile, and insulin resistance in young obese women N Mezghanni, K Chaabouni, H Chtourou, L Masmoudi, K Chamari, ... African Journal of Microbiology Research 6 (10), 2481-2488, 2012 | 26 | 2012 |
| Association analysis of IL1 gene polymorphisms in autoimmune thyroid diseases in the Tunisian population M Kammoun-Krichen, N Bougacha-Elleuch, K Makni, M Rebai, A Rebai, ... European cytokine network 18 (4), 17-21, 2007 | 26 | 2007 |
| Gonadal dysgenesis and the Mayer-Rokitansky-Kuster-Hauser Syndrome in a girl with a 46, XX karyotype: A case report and review of literature S Kebaili, K Chaabane, MF Mnif, M Kamoun, FH Kacem, N Guesmi, ... Indian journal of endocrinology and metabolism 17 (3), 505, 2013 | 25 | 2013 |
