Search Results - "Kacem, Faten"

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

    “…Purpose Congenital hypogonadotropic hypogonadism (CHH) is a rare genetic disorder mostly characterized by gonadotropins release and/or action deficiencies…”
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    Adrenal Diseases During Pregnancy: Pathophysiology, Diagnosis and Management Strategies by Kamoun, Mahdi, MD, Mnif, Mouna F., PhD, Charfi, Nadia, PhD, Kacem, Faten H., MD, Naceur, Basma B., MD, Mnif, Fatma, PhD, Dammak, Mohamed, MD, Rekik, Nabila, PhD, Abid, Mohamed, PhD

    “…Abstract Adrenal diseases—including disorders such as Cushing's syndrome, Addison's disease, pheochromocytoma, primary hyperaldosteronism and congenital…”
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    Analysis of ProP1 Gene in a Cohort of Tunisian Patients with Congenital Combined Pituitary Hormone Deficiency by Moalla, Mariam, Mnif-Feki, Mouna, Safi, Wajdi, Charfi, Nadia, Mejdoub-Rekik, Nabila, Abid, Mohamed, Hadj Kacem, Faten, Hadj Kacem, Hassen

    Published in Journal of clinical medicine (19-12-2022)
    “…Background: Non-syndromic combined pituitary hormone deficiency (CPHD) occurs due to defects in transcription factors that govern early pituitary development…”
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    Case report: Management challenges of late diagnosed 17‐alpha hydroxylase deficiency by 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

    Published in Clinical case reports (01-02-2023)
    “…Herein we report the intriguing case of a 42‐year‐old woman presenting with grade three hypertension, severe hypokalemia and primary amenorrhea, which revealed…”
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    Is moderate-intensity interval training more tolerable than high-intensity interval training in adults with obesity? by Maaloul, Rami, Ben Dhia, Imen, Marzougui, Houssem, Turki, Mouna, Kacem, Faten, Makhlouf, Rihab, Amar, Mohamed, Kallel, Choumous, Driss, Tarak, Elleuch, Mohamed, Ayadi, Fatma, Ghroubi, Sameh, Hammouda, Omar

    Published in Biology of sport (01-01-2023)
    “…Interval training (IT) has been shown to be a time-effective alternative to traditional training programmes in the management of obesity. Nevertheless, studies…”
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    Tunisian Maturity-Onset Diabetes of the Young: A Short Review and a New Molecular and Clinical Investigation by Moalla, Mariam, Safi, Wajdi, Babiker Mansour, Maab, Hadj Kacem, Mohamed, Mahfood, Mona, Abid, Mohamed, Kammoun, Thouraya, Hachicha, Mongia, Mnif-Feki, Mouna, Hadj Kacem, Faten, Hadj Kacem, Hassen

    Published in Frontiers in endocrinology (Lausanne) (29-07-2021)
    “…Maturity-Onset Diabetes of the Young (MODY) is a monogenic non-autoimmune diabetes with 14 different genetic forms. MODY-related mutations are rarely found in…”
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    Pheochromocytoma of the prostate: An unusual location by Hadj Kacem, Faten, Boujelben, Khouloud, Feki, Wiem, Chaabouni, Khansa, Charfi, Nadia, Abid, Mohamed

    Published in Urology case reports (01-07-2022)
    “…Ectopic pheochromocytomas, also called paragangliomas, are defined as catecholamine -secreting tumors, which develop outside the adrenal medulla…”
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    Diabetes Distress and Illness Perceptions in Tunisian Type 2 Diabetes Patients by Masmoudi, Rim, Kacem, Faten Hadj, Bouattour, Maroua, Guermazi, Fatma, Sellami, Rim, Feki, Ines, Mnif, Mouna, Masmoudi, Jawaher, Baati, Imen, Abid, Mohamed

    Published in Diabetes, metabolic syndrome and obesity (30-11-2023)
    “…Purpose: Diabetes distress (DD) refers to the negative emotions and burden of living with diabetes. Illness perceptions are among the factors that can…”
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    Genetic analysis of Turner syndrome in Tunisian patients: from diagnosis to management by Siala-Sahnoun, Olfa, Laadhar, Fatma, Mnif, Mouna, Sefi, Wajdi, Kacem, Faten, Kessentini, Mohamed, Abid, Mohamed, Fakhfakh, Faiza

    “…Background/aim Turner syndrome (TS) is a rare sex chromosome abnormality in women, occurring in approximately one in 2500 live births, associated with a wide…”
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    Insulinoma with equivocal imaging by Belabed, Wafa, Mnif, Fatma, Missaoui, Abdel Mouhaymen, Elleuch, Mouna, Ben Salah, Dhoha, Charfi, Nadia, Mnif, Mouna, Rekik, Nabila, Hadj Kacem, Faten, Abid, Mohamed

    “…Summary A 55-year-old patient was admitted to our department for the management of a repetitive alteration of consciousness. Biological investigation results…”
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    Cardiothyreosis: Epidemiological, clinical and therapeutic approach by 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

    Published in Clinical Medicine Insights. Cardiology (01-01-2023)
    “…Introduction: Cardiothyreosis corresponds to the cellular effects of free thyroid hormones on the vascular wall and the myocardium. We aim to describe the…”
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    A Rare Cause of Refractory Chronic Diarrhea and Cachexia: A Case Report by Hadj Kacem, Faten, Chebbi, Donia, Chakroun, Amal, Charfi, Nadia, Ghorbel, Dorra, Mnif, Fatma, Mnif, Mouna, Rekik, Nabila, Abid, Mohamed

    Published in Iranian journal of public health (01-02-2020)
    “…VIPoma is an unusual neuroendocrine neoplasm that autonomously secretes VIP. It is associated with secretory diarrhea and electrolyte disturbances. Herein we…”
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    Congenital hypopituitarism in familial Turner syndrome cases caused by a highly prevalent PROP1 gene mutation in Tunisia by Hadj Kacem, Hassen, Moalla, Mariam, Hadj Kacem, Faten, Trimeche, Oumeyma, Safi, Wajdi, Mnif-Feki, Mouna, Abid, Mohamed

    Published in Endocrine and metabolic science (31-03-2024)
    “…Turner syndrome (TS) is a genetic disorder found only in females who are completely or partially missing an X chromosome. It is rarely inherited from parent to…”
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    Presentation and management of pheochromocytomas and paragangliomas: about 40 cases by kacem, Faten Hadj, Salah, Ameni, Fathallah, Bilel, Boujelben, Khouloud, Charfi, Nadia, Abid, Mohamed

    Published in African journal of urology (01-12-2021)
    “…Background Pheochromocytoma and paraganglioma are rare neuroendocrine tumors of the chromaffin tissue, which may produce catecholamines. The aim of our study…”
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    Neurological Characteristics of Allgrove Syndrome: A Case Series by 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

    Published in Annals of child neurology (01-04-2024)
    “…Purpose: Allgrove syndrome, also known as “triple A” syndrome, is characterized by adrenal insufficiency, achalasia, and alacrimia. When neurological signs are…”
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    Diagnosis and management of pituitary apoplexy: a Tunisian data by Hadj Kacem, Faten, Trimeche, Oumeyma, Gargouri, Imen, Ben Salah, Dhoha, Charfi, Nadia, Rekik, Nabila, Mnif, Fatma, Mnif, Mouna, Elleuch, Mouna, Abid, Mohammed

    Published in Chinese neurosurgical journal (01-07-2023)
    “…Pituitary apoplexy (PA) is defined as the hemorrhage or the infraction of a pituitary adenoma. Aiming to determine the epidemiological, clinical, paraclinical…”
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    Isolated adrenocorticotropic hormone deficiency due to probable lymphocytic hypophysitis in a woman by Kacem, Faten Hadj, Charfi, Nadia, Mnif, Mouna Feki, Kamoun, Mahdi, Akid, Faouzi, Mnif, Fatma, Naceur, Basma Ben, Rekik, Nabila, Mnif, Zainab, Abid, Mohamed

    “…We report a 22-year-old woman who presented with asthenia, weight loss and hypotension in which extensive pituitary and adrenal investigations were diagnostic…”
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