Search Results - "Kacem, Faten"
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Unlocking the power of synergy: High-intensity functional training and early time-restricted eating for transformative changes in body composition and cardiometabolic health in inactive women with obesity
Published in PloS one (01-05-2024)“…The purpose of this study was to examine the long-term effects of time-restricted eating (TRE), with or without high intensity functional training (HIFT), on…”
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Nonstop mutation in the Kisspeptin 1 receptor (KISS1R) gene causes normosmic congenital hypogonadotropic hypogonadism
Published in Journal of assisted reproduction and genetics (01-06-2019)“…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
Published in The American journal of the medical sciences (01-01-2014)“…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
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
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?
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
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
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
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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Potential role of liver enzyme levels as predictive markers of glucose metabolism disorders in a Tunisian population
Published in Canadian journal of physiology and pharmacology (01-11-2018)“…The relationship between liver enzymes and T2D risk is inconclusive. We aimed to evaluate the association between liver markers and risk of carbohydrate…”
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Genetic analysis of Turner syndrome in Tunisian patients: from diagnosis to management
Published in Journal of the Arab Society for Medical Research (01-01-2023)“…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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Correction: Unlocking the power of synergy: High-intensity functional training and early time-restricted eating for transformative changes in body composition and cardiometabolic health in inactive women with obesity
Published in PloS one (31-05-2024)“…[This corrects the article DOI: 10.1371/journal.pone.0301369.]…”
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Insulinoma with equivocal imaging
Published in Endocrinology, diabetes & metabolism case reports (01-04-2023)“…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
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
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
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
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
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
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
Published in Indian journal of endocrinology and metabolism (01-10-2013)“…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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