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

Insulinome associé à une insuffisance corticotrope et un hypogonadisme hypergondadotrope: à propos d’une observation

por Hadjkacem, Faten, Kalthoum, Mahdi, Ghorbel, Dorra, Ammar, Mouna, Elleuch, Mouna, Charfi, Nadia, Mnif, Mouna, Abid, Mohamed
Publicado 2019

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

The first concurrent detection of mitochondrial DNA m.3243A>G mutation, deletion, and depletion in a family with mitochondrial diabetes

por Tabebi, Mouna, Safi, Wajdi, Felhi, Rahma, Alila Fersi, Olfa, Keskes, Leila, Abid, Mohamed, Mnif, Mouna, Fakhfakh, Faiza
Publicado 2020

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

SLC26A4 Variations Among Graves’ Hyper-Functioning Thyroid Gland

por Hadj-Kacem, Hassen, Kallel, Rihab, Belguith-Maalej, Salima, Mnif, Mouna, Charfeddine, Ilhem, Ghorbel, Abdelmounem, Abid, Mohamed, Ayadi, Hammadi, Masmoudi, Saber
Publicado 2010

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

Diabetes Distress and Illness Perceptions in Tunisian Type 2 Diabetes Patients

por Masmoudi, Rim, Hadj Kacem, Faten, Bouattour, Maroua, Guermazi, Fatma, Sellami, Rim, Feki, Ines, Mnif, Mouna, Masmoudi, Jawaher, Baati, Imen, Abid, Mohamed
Publicado 2023

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

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

por Chabchoub, Ghazi, Uz, Elif, Maalej, Abdellatif, Mustafa, Chigdem A, Rebai, Ahmed, Mnif, Mouna, Bahloul, Zouheir, Farid, Nadir R, Ozcelik, Tayfun, Ayadi, Hammadi
Publicado 2009

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

Gonadal dysgenesis and the Mayer-Rokitansky-Kuster-Hauser Syndrome in a girl with a 46, XX karyotype: A case report and review of literature

por Kebaili, Sahbi, Chaabane, Kais, Mnif, Mouna Feki, Kamoun, Mahdi, Kacem, Faten Hadj, Guesmi, Nouha, Gassara, Hichem, Dammak, Abdallah, Louati, Doulira, Amouri, Habib, Guermazi, Mohamed
Publicado 2013

A 20 year history of clinical and genetic study of thyroid autoimmunity in a Tunisian multigenerational family: Evidence for gene interaction()

por Bougacha-Elleuch, Noura, Charfi, Nadia, Kharrat, Najla, Ayadi, Fatma, Maalej, Abdellatif, Chabchoub, Ghazi, Rebai, Ahmed, Kammoun-Krichen, Maha, Belguith-Maalej, Salima, Abid, Mohamed, Mnif, Mouna, Ayadi, Hammadi
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