Zobrazeno 1 - 10
of 135
pro vyhledávání: '"B. Maalej"'
Autor:
W. Haouari, S. Omri, A. Labyadh, R. Feki, I. Gassara, L. Zouari, J. Ben Thabet, N. Charfi, M. B. Maalej, N. Smaoui, M. Maalej
Publikováno v:
European Psychiatry, Vol 67, Pp S163-S163 (2024)
Introduction Conjugal homicide refers to the act of killing a current or former intimate life partner, regardless of their marital status. This type of behavior is still inadequately addressed by prevention programs, as it is often regarded as except
Externí odkaz:
https://doaj.org/article/11ce48e842fb442eb5447be44628b07e
Autor:
W. Haouari, S. Omri, A. Labyadh, R. Feki, I. Gassara, N. Charfi, J. Ben Thabet, M. B. Maalej, N. Smaoui, L. Zouari, M. Maalej
Publikováno v:
European Psychiatry, Vol 67, Pp S829-S830 (2024)
Introduction Emigration has a substantial impact on Tunisia’s healthcare sector. Graduates, including medical students at different educational levels, as well as general practitioners and specialists, often choose to emigrate. Some do so to pursue
Externí odkaz:
https://doaj.org/article/6f64cd7dc5404422b733e5b13bda56b8
Autor:
W. Haouari, S. Omri, A. Labyadh, I. Gassara, R. Feki, N. Charfi, J. Ben Thabet, M. B. Maalej, N. Smaoui, L. Zouari, M. Maalej
Publikováno v:
European Psychiatry, Vol 67, Pp S830-S830 (2024)
Introduction The burnout syndrome is a blend of physical exhaustion and emotional fatigue that impairs an individual’s performance at work. In Tunisia, factors like working hours, the frequency of monthly shifts, and the physical and emotional abus
Externí odkaz:
https://doaj.org/article/22f8046e42c84f5ea1cfa75ac0b0afec
Autor:
W. Haouari, S. Omri, A. Labyadh, R. Feki, I. Gassara, N. Smaoui, J. Ben Thabet, M. B. Maalej, M. Maalej, N. Charfi, L. Zouari
Publikováno v:
European Psychiatry, Vol 67, Pp S487-S487 (2024)
Introduction While postictal mania is a well-recognized clinical condition, it has received less research attention compared to other postictal manifestations. Objectives Drawing upon an analysis of a case report that underscores the clinical and th
Externí odkaz:
https://doaj.org/article/e558a68af625401f8a6b1ab295ec6f05
Akademický článek
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Autor:
R. Belhadj, A. Ben Hlima, B. Maalej, Abdelmajid Mahfoudh, M. Weli, A. Elleuch, Thouraya Kamoun, Mohamed-Ridha Barbouche, Najla Mekki, Lamia Gargouri
Publikováno v:
Transfusion Clinique et Biologique. 27:61-64
Background and aim The aim of this study is to evaluate the clinical, biological and hematological profiles of autoimmune hemolytic anemia (AIHA) in children and to specify its etiologies, therapeutic modalities, and treatment responses. Methods This
Autor:
B. Maalej, Abdelatif Gargouri, Imen Moalla, Mohamed Abid, Faiza Safi, Manel Charfi, Abdelmajid Mahfouth, Sahar Trichili, Lamia Gargouri, Feten Haj kacem, Manel Weli
Publikováno v:
Abstracts.
Introduction Takayasu arteritis is an idiopathic chronic granulomatous panarteritis predominantly affecting the aorta and its main branches. The diagnosis is based on a set of clinical, biological and radiological criteria. Observation Thes are two g
Autor:
Lamia Gargouri, B. Maalej, Manel Wali, Faiza Safi, Abdelatif Gargouri, Abdelmajid Mahfoudh, Manel Hsairi, Muhamed Muzaker, Chiraz Regaieg, Imene Moalla
Publikováno v:
Abstracts.
Introduction Primary immunodeficiency disorders (PIDs) in children are genetic diseases that affect adaptive or innate immunity. The importance and nature of the clinical signs depend on the deficit function predominantly within the immune system. Ob
Autor:
A. Elleuch, B. Ben Amar, R. Zaghdoud, Jamel Damak, B. Maalej, M. Ben Yahya, M. Weli, Abdelmajid Mahfoudh, Yosra Mejdoub, Lamia Gargouri
Publikováno v:
Médecine et Maladies Infectieuses. 50:S159
Introduction L’adenophlegmon est la suppuration d’un ganglion lymphatique de la chaine jugulo-carotidienne siegeant dans le territoire de drainage d’une porte d’entree microbienne en particulier une infection rhino-pharyngee. C’est une comp
Autor:
Jamel Mnif, Neila Belguith, Mongia Hachicha, Imen Chabchoub, Habiba Chaabouni, B. Maalej, Lamia Ben Mansour, Mariam Chaabouni, Thouraya Kamoun, Khaireddine Ben Mahfoudh
Publikováno v:
Journal of Pediatric Neurology. :387-390
Miller-Dieker syndrome (MDS) is a gene deletion syndrome. It includes severe lissencephaly and a characteristic phenotypic appearance. Children with MDS also suffer from severe mental retardation, growth delay, epilepsy and occasionally hypsarrythmia