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Nozha Kallel

No Evidence of a Detrimental Effect of Cabergoline Therapy on Cardiac Valves in Patients with Acromegaly
2012 · Luigi Maione, Cyril Garcia, et al. · The Journal of Clinical Endocrinology & Metabolism · 70
Long-Term Outcome of Patients With Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency
2012 · Mouna Feki Mnif, Mahdi Kamoun, et al. · The American Journal of the Medical Sciences · 52
The mitochondrial ND1 m.3337G>A mutation associated to multiple mitochondrial DNA deletions in a patient with Wolfram syndrome and cardiomyopathy
2011 · Najla Mezghani, Mouna Mnif, et al. · Biochemical and Biophysical Research Communications · 26
Brain magnetic resonance imaging findings in adult patients with congenital adrenal hyperplasia: Increased frequency of white matter impairment and temporal lobe structures dysgenesis
2013 · Mouna Feki Mnif, Mahdi Kamoun, et al. · Indian Journal of Endocrinology and Metabolism · 25
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
2013 · Najla Mezghani, Mouna Mnif, et al. · Biochemical and Biophysical Research Communications · 21
Leydig Cell Tumor Associated with Testicular Adrenal Rest Tumors in a Patient with Congenital Adrenal Hyperplasia due to 11 β -Hydroxylase Deficiency
2012 · Nadia Charfi, Mahdi Kamoun, et al. · Case Reports in Urology · 19
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Metabolic profile and cardiovascular risk factors in adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
2012 · Mouna Feki Mnif, Mahdi Kamoun, et al. · Indian Journal of Endocrinology and Metabolism · 17
Adrenocortical Secreting Mass in a Patient with Gardner's Syndrome: A Case Report
2010 · Nabila Mejdoub Rekik, Sourour Ben Salah, et al. · Case Reports in Medicine · 12
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Clinical characteristics and outcomes of critically ill COVID-19 patients in Sfax, Tunisia
2021 · Mabrouk Bahloul, Sana Kharrat, et al. · Acute and Critical Care · 11
A whole mitochondrial genome screening in a MELAS patient: A novel mitochondrial tRNAVal mutation
2011 · Najla Mezghani, Mouna Mnif, et al. · Biochemical and Biophysical Research Communications · 6
Thymic plasmacytoma presenting as polyneuropathy and revealing multiple myeloma: a case report
2022 · Syrine Laroussi, Khadija Sonda Moalla, et al. · The Egyptian Journal of Neurology Psychiatry and Neurosurgery
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Works count: 11
Citation count: 259
H-index: 9
I10-index: 9
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