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Fatma Mnif

Showing results (21-30 of 31) with videos related to

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Indian Journal of Endocrinology and Metabolism|November 20, 2013
Isolated adrenocorticotropic hormone deficiency due to probable lymphocytic hypophysitis in a womanFaten Hadj Kacem, Nadia Charfi, Mouna Feki Mnif, et al.
Metabolic Syndrome and Related Disorders|January 17, 2024
Metabolic Disorders During ProlactinomasMouna Elleuch, Molka Ben Bnina, Fatma Loukil, et al.
Indian Journal of Endocrinology and Metabolism|December 11, 2012
Metabolic profile and cardiovascular risk factors in adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiencyMouna Feki Mnif, Mahdi Kamoun, Fatma Mnif, et al.
Human Immunology|April 28, 2012
Non-HLA autoimmunity genetic factors contributing to Autoimmune Polyglandular Syndrome type II in Tunisian patientsHajer Fourati, Dorra Bouzid, Olfa Abida, et al.
Endocrine Regulations|March 31, 2026
One genotype with a myriad of phenotypes: A family with multiple endocrine neoplasiaOumeyma Trimeche, Fatma Mnif, Fatma Abdelhedi, et al.
Annals of Diagnostic Pathology|March 16, 2010
Ganglioneuroma of adrenal gland in a patient with Turner syndromeMahdi Kamoun, Mouna Feki Mnif, Nabila Rekik, et al.
The American Journal of the Medical Sciences|January 25, 2012
Long-term outcome of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiencyMouna Feki Mnif, Mahdi Kamoun, Fatma Mnif, et al.
Case Reports in Urology|May 19, 2012
Leydig Cell Tumor Associated with Testicular Adrenal Rest Tumors in a Patient with Congenital Adrenal Hyperplasia due to 11β-Hydroxylase DeficiencyNadia Charfi, Mahdi Kamoun, Mouna Feki Mnif, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|July 15, 2022
A novel thymidine phosphorylase mutation in a family with Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): Molecular docking, dynamic simulation and computational investigationsMarwa Ammar, Wajdi Safi, Abdelaziz Tlili, et al.
Indian Journal of Endocrinology and Metabolism|June 19, 2013
Brain magnetic resonance imaging findings in adult patients with congenital adrenal hyperplasia: Increased frequency of white matter impairment and temporal lobe structures dysgenesisMouna Feki Mnif, Mahdi Kamoun, Fatma Mnif, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Indian Journal of Endocrinology and Metabolism|November 20, 2013
Isolated adrenocorticotropic hormone deficiency due to probable lymphocytic hypophysitis in a womanFaten Hadj Kacem, Nadia Charfi, Mouna Feki Mnif, et al.
Metabolic Syndrome and Related Disorders|January 17, 2024
Metabolic Disorders During ProlactinomasMouna Elleuch, Molka Ben Bnina, Fatma Loukil, et al.
Indian Journal of Endocrinology and Metabolism|December 11, 2012
Metabolic profile and cardiovascular risk factors in adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiencyMouna Feki Mnif, Mahdi Kamoun, Fatma Mnif, et al.
Human Immunology|April 28, 2012
Non-HLA autoimmunity genetic factors contributing to Autoimmune Polyglandular Syndrome type II in Tunisian patientsHajer Fourati, Dorra Bouzid, Olfa Abida, et al.
Endocrine Regulations|March 31, 2026
One genotype with a myriad of phenotypes: A family with multiple endocrine neoplasiaOumeyma Trimeche, Fatma Mnif, Fatma Abdelhedi, et al.
Annals of Diagnostic Pathology|March 16, 2010
Ganglioneuroma of adrenal gland in a patient with Turner syndromeMahdi Kamoun, Mouna Feki Mnif, Nabila Rekik, et al.
The American Journal of the Medical Sciences|January 25, 2012
Long-term outcome of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiencyMouna Feki Mnif, Mahdi Kamoun, Fatma Mnif, et al.
Case Reports in Urology|May 19, 2012
Leydig Cell Tumor Associated with Testicular Adrenal Rest Tumors in a Patient with Congenital Adrenal Hyperplasia due to 11β-Hydroxylase DeficiencyNadia Charfi, Mahdi Kamoun, Mouna Feki Mnif, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|July 15, 2022
A novel thymidine phosphorylase mutation in a family with Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): Molecular docking, dynamic simulation and computational investigationsMarwa Ammar, Wajdi Safi, Abdelaziz Tlili, et al.
Indian Journal of Endocrinology and Metabolism|June 19, 2013
Brain magnetic resonance imaging findings in adult patients with congenital adrenal hyperplasia: Increased frequency of white matter impairment and temporal lobe structures dysgenesisMouna Feki Mnif, Mahdi Kamoun, Fatma Mnif, et al.
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