Unlocking the power of synergy: High-intensity functional training and early time-restricted eating for transformative changes in body composition and cardiometabolic health in ina... von Ameur, Ranya, Maaloul, Rami, Tagougui, Sémah, Neffati, Fadoua, Hadj Kacem, Faten, Najjar, Mohamed Fadhel, Ammar, Achraf, Hammouda, Omar

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Nonstop mutation in the Kisspeptin 1 receptor (KISS1R) gene causes normosmic congenital hypogonadotropic hypogonadism von Moalla, Mariam, Hadj Kacem, Faten, Al-Mutery, Abdullah Fahad, Mahfood, Mona, Mejdoub-Rekik, Nabila, Abid, Mohamed, Mnif-Feki, Mouna, Hadj Kacem, Hassen

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Tunisian Maturity-Onset Diabetes of the Young: A Short Review and a New Molecular and Clinical Investigation von Moalla, Mariam, Safi, Wajdi, Mansour, Maab Babiker, Kacem, Mohamed Hadj, Mahfood, Mona, Abid, Mohamed, Kammoun, Thouraya, Hachicha, Mongia, Mnif-Feki, Mouna, Kacem, Faten Hadj, Kacem, Hassen Hadj

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Analysis of ProP1 Gene in a Cohort of Tunisian Patients with Congenital Combined Pituitary Hormone Deficiency von Moalla, Mariam, Mnif-Feki, Mouna, Safi, Wajdi, Charfi, Nadia, Mejdoub-Rekik, Nabila, Abid, Mohamed, Hadj Kacem, Faten, Hadj Kacem, Hassen

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Autoimmune thyroiditis associated with autoimmune diseases von Ben Salah, Raida, Hadj Kacem, Faten, Soomauro, Siddiqa, Chouaib, Sarra, Frikha, Faten, Charfi, Nedia, Abid, Mohamed, Bahloul, Zouhir

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

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Pheochromocytoma of the prostate: An unusual location von Hadj Kacem, Faten, Boujelben, Khouloud, Feki, Wiem, Chaabouni, Khansa, Charfi, Nadia, Abid, Mohamed

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Cardiothyreosis: Epidemiological, clinical and therapeutic approach von Mouna, Elleuch, Molka, Ben Bnina, Sawssan, Ben teber, Dhoha, Ben salah, Khouloud, Boujelbene, Nadia, Charfi, Fatma, Mnif, Mouna, Mnif, Nabila, Rekik, Faten, Hadj Kacem, Mohamed, Abid

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A Rare Cause of Refractory Chronic Diarrhea and Cachexia: A Case Report von Kacem, Faten Hadj, Chebbi, Donia, Chakroun, Amal, Charfi, Nadia, Ghorbel, Dorra, Mnif, Fatma, Mnif, Mouna, Rekik, Nabila, Abid, Mohamed

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Correction: Unlocking the power of synergy: High-intensity functional training and early time-restricted eating for transformative changes in body composition and cardiometabolic h... von Ameur, Ranya, Maaloul, Rami, Tagougui, Sémah, Neffati, Fadoua, Kacem, Faten Hadj, Najjar, Mohamed Fadhel, Ammar, Achraf, Hammouda, Omar

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Congenital hypopituitarism in familial Turner syndrome cases caused by a highly prevalent PROP1 gene mutation in Tunisia von Hadj Kacem, Hassen, Moalla, Mariam, Hadj Kacem, Faten, Trimeche, Oumeyma, Safi, Wajdi, Mnif-Feki, Mouna, Abid, Mohamed

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Diabetes Distress and Illness Perceptions in Tunisian Type 2 Diabetes Patients von Masmoudi, Rim, Kacem, Faten Hadj, Bouattour, Maroua, Guermazi, Fatma, Sellami, Rim, Feki, Ines, Mnif, Mouna, Masmoudi, Jawaher, Baati, Imen, Abid, Mohamed

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Presentation and management of pheochromocytomas and paragangliomas: about 40 cases von kacem, Faten Hadj, Salah, Ameni, Fathallah, Bilel, Boujelben, Khouloud, Charfi, Nadia, Abid, Mohamed

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Insulinoma with equivocal imaging von Belabed, Wafa, Mnif, Fatma, Missaoui, Abdel Mouhaymen, Elleuch, Mouna, Ben Salah, Dhoha, Charfi, Nadia, Mnif, Mouna, Rekik, Nabila, Hadj Kacem, Faten, Abid, Mohamed

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Neurological Characteristics of Allgrove Syndrome: A Case Series von Salah, Dhoha Ben, Elleuch, Mouna, Trimeche, Oumeyma, Zargni, Asma, Kallabi, Fakhri, Sakka, Salma, Mnif, Fatma, Rekik, Nabila, Charfi, Nadia, Kamoun, Hassen, Feki, Mouna Mnif, Kacem, Faten Hadj, Abid, Mohamed

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Genetic analysis of Turner syndrome in Tunisian patients: from diagnosis to management von Siala-Sahnoun, Olfa, Laadhar, Fatma, Mnif, Mouna, Sefi, Wajdi, Kacem, Faten, Kessentini, Mohamed, Abid, Mohamed, Fakhfakh, Faiza

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Diagnosis and management of pituitary apoplexy: a Tunisian data von Hadj Kacem, Faten, Trimeche, Oumeyma, Gargouri, Imen, Ben Salah, Dhoha, Charfi, Nadia, Rekik, Nabila, Mnif, Fatma, Mnif, Mouna, Elleuch, Mouna, Abid, Mohammed

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Isolated adrenocorticotropic hormone deficiency due to probable lymphocytic hypophysitis in a woman von Kacem, Faten Hadj, Charfi, Nadia, Mnif, Mouna Feki, Kamoun, Mahdi, Akid, Faouzi, Mnif, Fatma, Naceur, Basma Ben, Rekik, Nabila, Mnif, Zainab, Abid, Mohamed

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Molecular mechanisms underlying the defects of two novel mutations in the HSD17B3 gene found in the Tunisian population von Ben Rhouma, Bochra, Kley, Manuel, Kallabi, Fakhri, Kacem, Faten Hadj, Kammoun, Thouraya, Safi, Wajdi, Keskes, Leila, Mnif, Mouna, Odermatt, Alex, Belguith, Neila

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Reproductive outcomes of female patients with congenital adrenal hyperplasia due to 21-hydroxylase defi ciency von Mnif, Mouna, Kamoun, Mahdi, Kacem, Faten, Mnif, Fatma, Charfi, Nadia, Naceur, Basma, Rekik, Nabila, Abid, Mohamed

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