Zobrazeno 1 - 10
of 212
pro vyhledávání: '"Nadia Charfi"'
Autor:
Dhoha Ben Salah, Mouna Elleuch, Oumeyma Trimeche, Asma Zargni, Fakhri Kallabi, Salma Sakka, Fatma Mnif, Nabila Rekik, Nadia Charfi, Hassen Kamoun, Mouna Mnif Feki, Faten Hadj Kacem, Mohamed Abid
Publikováno v:
Annals of Child Neurology, Vol 32, Iss 2, Pp 130-134 (2024)
Purpose Allgrove syndrome, also known as “triple A” syndrome, is characterized by adrenal insufficiency, achalasia, and alacrimia. When neurological signs are also present, the condition is referred to as “4 A” syndrome. Methods We conducted
Externí odkaz:
https://doaj.org/article/047022b12fb7477588ee364b1bf1b2b8
Autor:
Faten Hadj Kacem, Oumeyma Trimeche, Imen Gargouri, Dhoha Ben Salah, Nadia Charfi, Nabila Rekik, Fatma Mnif, Mouna Mnif, Mouna Elleuch, Mohammed Abid
Publikováno v:
Chinese Neurosurgical Journal, Vol 9, Iss 1, Pp 1-7 (2023)
Abstract Background Pituitary apoplexy (PA) is defined as the hemorrhage or the infraction of a pituitary adenoma. Aiming to determine the epidemiological, clinical, paraclinical characteristics as well as management and outcomes of PA in our populat
Externí odkaz:
https://doaj.org/article/9027a38e022145f2be46b788ff1250d0
Autor:
Wafa Belabed, Fatma Mnif, Abdel Mouhaymen Missaoui, Mouna Elleuch, Dhoha Ben Salah, Nadia Charfi, Mouna Mnif, Nabila Rekik, Faten Hadj Kacem, Mohamed Abid
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-4 (2023)
A 55-year-old patient was admitted to our department for the management of a repetitive alteration of consciousness. Biological investigation results were consistent with endogenous hyperinsulinemic hypoglycemia. Insulinoma was therefore suspected. A
Externí odkaz:
https://doaj.org/article/c71dca440e6849f2b2136ea81abfcaae
Autor:
Dhoha Ben Salah, Oumeyma Trimeche, Mouna Elleuch, Wafa El abed, Ameni Salah, Fatma Abdelhadi, Hassen Kammoun, Wiem Feki, Zeineb Mnif, Khansa Chaabouni, Fatma Ayedi, Fatma Mnif, Nabila Rekik, Mouna Mnif, Nadia Charfi, Faten Hadj kacem, Mohamed Abid
Publikováno v:
Clinical Case Reports, Vol 11, Iss 2, Pp n/a-n/a (2023)
Abstract Herein we report the intriguing case of a 42‐year‐old woman presenting with grade three hypertension, severe hypokalemia and primary amenorrhea, which revealed to be the complete form of 17 alphahydroxylase deficiency. We also discuss th
Externí odkaz:
https://doaj.org/article/fa3765463d944ba885cd3dc7abe94aed
Autor:
Faten Hadj kacem, Ameni Salah, Bilel Fathallah, Khouloud Boujelben, Nadia Charfi, Mohamed Abid
Publikováno v:
African Journal of Urology, Vol 27, Iss 1, Pp 1-6 (2021)
Abstract Background Pheochromocytoma and paraganglioma are rare neuroendocrine tumors of the chromaffin tissue, which may produce catecholamines. The aim of our study was to analyze the clinical and para-clinical aspects as well as the therapeutic an
Externí odkaz:
https://doaj.org/article/427960ac82e94e3ebf5b359bc8f1a9ca
Autor:
Faten Hadj Kacem, Khouloud Boujelben, Wiem Feki, Khansa Chaabouni, Nadia Charfi, Mohamed Abid
Publikováno v:
Urology Case Reports, Vol 43, Iss , Pp 102108- (2022)
Ectopic pheochromocytomas, also called paragangliomas, are defined as catecholamine -secreting tumors, which develop outside the adrenal medulla.Pheochromocytomas of the urinary tract represent less than 1% of all paragangliomas and are most commonly
Externí odkaz:
https://doaj.org/article/df697627b1844151a943e03893e94b45
Autor:
Imen Maaloul, Marwa Moussaoui, Ameni Salah, Wiem Feki, Hela Fourati, Nadia Charfi, Zeineb Mnif
Publikováno v:
Case Reports in Radiology, Vol 2021 (2021)
Introduction. Meningeal melanocytoma (MM) is a very rare neuroectodermal neoplasm arising from the leptomeninges. Primary suprasellar melanocytomas are exceedingly rare, with only a handful of cases reported. The systemic spread of a nontransformed m
Externí odkaz:
https://doaj.org/article/29fac0d6032a4663b33bcdd1b5ae6722
Autor:
Faten HADJ KACEM, Donia CHEBBI, Amal CHAKROUN, Nadia CHARFI, Dorra GHORBEL, Fatma MNIF, Mouna MNIF, Nabila REKIK, Mohamed ABID
Publikováno v:
Iranian Journal of Public Health, Vol 49, Iss 2 (2020)
VIPoma is an unusual neuroendocrine neoplasm that autonomously secretes VIP. It is associated with secretory diarrhea and electrolyte disturbances. Herein we report a case of a male patient, who was hospitalized in the Department of Endocrinology in
Externí odkaz:
https://doaj.org/article/e4235440e3d142a99351ba5b2eb4bbb2
Autor:
Hamza Elfekih, Faten Hadjkacem, Mouna Elleuch, Dorra Ghorbel, Nadia Charfi, Fatma Mnif, Nabila Rekik, Mouna Mnif, Mohamed Abid
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 18, Iss 5 (2019)
Insulin therapy is an essential treatment for type 1 and uncontrolled type 2 diabetes mellitus (DM). Hypersensitivity reactions have been described since the first administration of insulin, the same as any other therapy. Despite being a rare situati
Externí odkaz:
https://doaj.org/article/40d6a50f2fff439db2550055edde83b8
Autor:
Faten Hadjkacem, Mahdi Kalthoum, Dorra Ghorbel, Mouna Ammar, Mouna Elleuch, Nadia Charfi, Mouna Mnif, Mohamed Abid
Publikováno v:
The Pan African Medical Journal, Vol 34, Iss 32 (2019)
L’insulinome pancréatique est une tumeur neuroendocrine rare, souvent bénigne, mais qui peut mettre en jeu le pronostic vital du fait des accidents hypoglycémiques qu’elle engendre. L'insuffisance surrénalienne peut aussi être responsable d'
Externí odkaz:
https://doaj.org/article/2e78e56e9aa04c8689a5f95c4056ed64