Adrenocortical Secreting Mass in a Patient with Gardner's Syndrome: A Case Report

por Rekik, Nabila Mejdoub, Ben Salah, Sourour, Kallel, Nozha, Kamoun, Mahdi, Charfi, Nadia, Abid, Mohamed
Publicado 2010

Mode de révélation inhabituel d’une hyperparathyroïdie primaire du sujet jeune: à propos de deux cas

por Salah, Dhoha Ben, Rekik, Nabila, Affes, Lilia, Elleuch, Mouna, Mnif, Fatma, Mnif, Mouna, Abid, Mohamed
Publicado 2018

Hyperthyroidism: A rare cause of pulmonary embolism: Report of two cases

por Grine, Sonia, Charfi, Nadia, Kamoun, Mahdi, Mnif, Fatma, Naceur, Basma Ben, Rekik, Nabila, Mnif, Mouna, Abid, Mohamed
Publicado 2013

Répercussions métaboliques et cardiovasculaires de la substitution glucocorticoïde au cours de la maladie d’Addison

por Salah, Dhoha Ben, Charfi, Nadia, Elleuch, Mouna, Kacem, Faten Hadj, Rekik, Nabila, Mnif, Mouna, Mnif, Fatma, Abid, Mohamed
Publicado 2018

Reproductive outcomes of female patients with congenital adrenal hyperplasia due to 21-hydroxylase defi ciency

por Mnif, Mouna Feki, Kamoun, Mahdi, Kacem, Faten Hadj, Mnif, Fatma, Charfi, Nadia, Naceur, Basma Ben, Rekik, Nabila, Abid, Mohamed
Publicado 2013

A Rare Cause of Refractory Chronic Diarrhea and Cachexia: A Case Report

por HADJ KACEM, Faten, CHEBBI, Donia, CHAKROUN, Amal, CHARFI, Nadia, GHORBEL, Dorra, MNIF, Fatma, MNIF, Mouna, REKIK, Nabila, ABID, Mohamed
Publicado 2020

Syndrome de Guillain Barré et décompensation acidocétosique du diabète au cours de la grossesse: a propos d’un cas et revue de la littérature

por Affes, Lilia, Elleuch, Mouna, Mnif, Fatma, Kacem, Faten Hadj, Salah, Dhouha Ben, Mnif, Mouna, Charfi, Nadia, Rekik, Nabila, Abid, Mohamed
Publicado 2017

Analysis of ProP1 Gene in a Cohort of Tunisian Patients with Congenital Combined Pituitary Hormone Deficiency

por Moalla, Mariam, Mnif-Feki, Mouna, Safi, Wajdi, Charfi, Nadia, Mejdoub-Rekik, Nabila, Abid, Mohamed, Hadj Kacem, Faten, Hadj Kacem, Hassen
Publicado 2022

Complicated urinary tract infections associated with diabetes mellitus: Pathogenesis, diagnosis and management

por Mnif, Mouna Feki, Kamoun, Mahdi, Kacem, Faten Hadj, Bouaziz, Zainab, Charfi, Nadia, Mnif, Fatma, Naceur, Basma Ben, Rekik, Nabila, Abid, Mohamed
Publicado 2013

Diagnosis and management of pituitary apoplexy: a Tunisian data

por Hadj Kacem, Faten, Trimeche, Oumeyma, Gargouri, Imen, Ben Salah, Dhoha, Charfi, Nadia, Rekik, Nabila, Mnif, Fatma, Mnif, Mouna, Elleuch, Mouna, Abid, Mohammed
Publicado 2023

Warthin-like papillary thyroid carcinoma: a case report and comprehensive review of the literature

por Missaoui, Abdel Mouhaymen, Hamza, Fatma, Belabed, Wafa, Mellouli, Manel, Maaloul, Mohamed, Charfi, Slim, Jardak, Issam, Sellami-Boudawara, Tahya, Rekik, Nabila, Abid, Mohamed
Publicado 2023

Insulinoma with equivocal imaging

por Belabed, Wafa, Mnif, Fatma, Missaoui, Abdel Mouhaymen, Elleuch, Mouna, Ben Salah, Dhoha, Charfi, Nadia, Mnif, Mouna, Rekik, Nabila, Hadj Kacem, Faten, Abid, Mohamed
Publicado 2023

Isolated adrenocorticotropic hormone deficiency due to probable lymphocytic hypophysitis in a woman

por Kacem, Faten Hadj, Charfi, Nadia, Mnif, Mouna Feki, Kamoun, Mahdi, Akid, Faouzi, Mnif, Fatma, Naceur, Basma Ben, Rekik, Nabila, Mnif, Zainab, Abid, Mohamed
Publicado 2013

Metabolic profile and cardiovascular risk factors in adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

por Mnif, Mouna Feki, Kamoun, Mahdi, Mnif, Fatma, Charfi, Nadia, Naceur, Basma Ben, Kallel, Nozha, Rekik, Nabila, Mnif, Zainab, Sfar, Mohamed Habib, Sfar, Mohamed Tahar, Hachicha, Mongia, Abid, Mohamed
Publicado 2012

Leydig Cell Tumor Associated with Testicular Adrenal Rest Tumors in a Patient with Congenital Adrenal Hyperplasia due to 11β-Hydroxylase Deficiency

por Charfi, Nadia, Kamoun, Mahdi, Feki Mnif, Mouna, Mseddi, Neila, Mnif, Fatma, Kallel, Nozha, Ben Naceur, Basma, Rekik, Nabila, Fourati, Hela, Daoud, Emna, Mnif, Zainab, Hadj Sliman, Mourad, Sellami-Boudawara, Tahia, Abid, Mohamed
Publicado 2012

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

por Mnif, Mouna Feki, Kamoun, Mahdi, Mnif, Fatma, Charfi, Nadia, Kallel, Nozha, Rekik, Nabila, Naceur, Basma Ben, Fourati, Hela, Daoud, Emna, Mnif, Zainab, Sfar, Mohamed Habib, Younes-Mhenni, Samia, Sfar, Mohamed Tahar, Hachicha, Mongia, Abid, Mohamed
Publicado 2013

Case report: Management challenges of late diagnosed 17‐alpha hydroxylase deficiency

por Ben Salah, Dhoha, Trimeche, Oumeyma, Elleuch, Mouna, El abed, Wafa, Salah, Ameni, Abdelhadi, Fatma, Kammoun, Hassen, Feki, Wiem, Mnif, Zeineb, Chaabouni, Khansa, Ayedi, Fatma, Mnif, Fatma, Rekik, Nabila, Mnif, Mouna, Charfi, Nadia, Hadj kacem, Faten, Abid, Mohamed
Publicado 2023