Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Oumeyma Trimeche"'
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:
Hassen Hadj Kacem, Mariam Moalla, Faten Hadj Kacem, Oumeyma Trimeche, Wajdi Safi, Mouna Mnif-Feki, Mohamed Abid
Publikováno v:
Endocrine and Metabolic Science, Vol 14, Iss , Pp 100160- (2024)
Background: 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 offspring and is not reported to be associated with any causal gene. In additi
Externí odkaz:
https://doaj.org/article/22a456da4b9d4fb087dbb6546bac6a30
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:
Imen Zemni, Amel Gara, Hadhba Nasraoui, Meriem Kacem, Amani Maatouk, Oumeyma Trimeche, Hela Abroug, Manel Ben Fredj, Cyrine Bennasrallah, Wafa Dhouib, Ines Bouanene, Asma Sriha Belguith
Publikováno v:
BMC Public Health, Vol 23, Iss 1, Pp 1-11 (2023)
Abstract Introduction The COVID-19 pandemic is regarded as a serious public health concern that boosts levels of stress and anxiety which could be explained by several reasons, including social isolation. In this regard, we aimed to assess the impact
Externí odkaz:
https://doaj.org/article/d685de6e080e4c78920a9c8edb2db213
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:
Kacem Akid Faten Haj, Oumeyma Trimeche, Mouna Mnif, Missaoui Abdel Mouhaymen, Salah Dhoha Ben, Mouna Elleuch, Mnif Fatma, Nadia Charfi, Majdoub Nabila Rekik, Mohamed Abid
Publikováno v:
Endocrine Abstracts.
Autor:
Kacem Akid Faten Haj, Oumeyma Trimeche, Mouna Mnif, Frikha Hamdi, Salah Dhoha Ben, Mouna Elleuch, Mnif Fatma, Nadia Charfi, Majdoub Nabila Rekik, Mohamed Abid
Publikováno v:
Endocrine Abstracts.
Autor:
Mnif Fatma, Oumeyma Trimeche, Missaoui Abdel Mouhaymen, Salah Dhoha Ben, Mouna Elleuch, Kacem Akid Faten Haj, Nadia Charfi, Mouna Mnif, Majdoub Nabila Rekik, Mohamed Abid
Publikováno v:
Endocrine Abstracts.
Autor:
Kacem Akid Faten Haj, Abdel Mouhaymen Missaoui, Siddiqa Soomauroo, Oumeyma Trimeche, Nabila Rekik Majdoub, Dhoha Ben Salah, Mohamed Abid Hedi
Publikováno v:
Endocrine Abstracts.
Autor:
faten Hadjkacem, Khouloud Boujelben, Oumeyma Trimeche, Faten Kallel, Maha Charfi, Mouna Mnif, Nadia Charfi, Nabila Rekik, Fatma Mnif, Dhouha Ben Salah, Mouna Elleuch, Moez Elloumi, Mohamed Abid
Langerhans Cell Histiocytosis (LCH) is a rare clinical condition of the mononuclear phagocyte system caused by abnormal clonal proliferation of aberrant histiocytes or Langerhans cells . We describe this by reporting a case of a 28-year-old male pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85939550c4aaabdb3f52113cd4a0faac
https://doi.org/10.22541/au.167655070.06379446/v1
https://doi.org/10.22541/au.167655070.06379446/v1