Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Mohamed Slim, Abdelmoula"'
Autor:
Zeineb Ben Ameur, Neji Tebib, Henda Kachouri, Sana Ben Messaoud, Yosra Sassi, Amel Ben Chehida, Maherzia Ferchichi, Mohamed Slim Abdelmoula, Rim Ben Abdelaziz, Hatem Azzouz
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 33:901-913
Objectives We investigated the quality of life (QOL) in parents of children with late treated phenylketonuria (PKU) and its associated factors. Methods We conducted a cross sectional study in the reference center of inherited metabolic disease in Tun
Publikováno v:
Journal of Clinical and Experimental Dentistry
Briki, Sondes ; Elleuch, Wael ; Karray, Fathi ; Abdelmoula, Mohamed ; Tanoubi, Issam. Cysts and tumors of the jaws treated by marsupialization : a description of 4 clinical cases. En: Journal of Clinical and Experimental Dentistry, 11 6 2019: 565-569
RODERIC. Repositorio Institucional de la Universitat de Valéncia
instname
Briki, Sondes ; Elleuch, Wael ; Karray, Fathi ; Abdelmoula, Mohamed ; Tanoubi, Issam. Cysts and tumors of the jaws treated by marsupialization : a description of 4 clinical cases. En: Journal of Clinical and Experimental Dentistry, 11 6 2019: 565-569
RODERIC. Repositorio Institucional de la Universitat de Valéncia
instname
Since the 4th edition of the World Health Organization's Classification of Head and Neck Tumours was published in January of 2017, the keratocystic odontogenic tumor is back into the cyst category as odontogenic keratocyst (OKC). Depending on the siz
Autor:
R. Ben Abdelaziz, A. Ben Chehida, Hatem Azzouz, S. Ben Messaoud, Mohamed Slim Abdelmoula, M. Lamouchi, Hela Boudabous, Neji Tebib, D. Ali Mohamed
Publikováno v:
Archives de Pédiatrie. 26:1-5
Purpose To describe the management of infants with epileptic spasms (ESs) in a low-income country and identify factors predictive of their prognosis. Material and methods We conducted a retrospective study in a university hospital in Tunis, Tunisia,
Autor:
Abdelkrim Rim, Afef Ben Thabet, Fathi Karray, Amira Bouraoui, Abdellatif Gargouri, Ridha Regaieg, Mohamed Slim Abdelmoula, Nedia Hmida, Chiraz Regaieg, Amel Ben Hmed
Publikováno v:
Abstracts.
Background Congenital epulis is a rare benign oral cavity tumor that usually arises from the maxillary alveolar mucosa. It is also known as congenital gingival granular cell tumor. This tumor can interfere with respiration and feeding. Prenatal diagn
Autor:
A. Slema, S. Ben Massaoud, A. Ben Chehida, R. Ben Abdelaziz, Mohamed Slim Abdelmoula, Neji Tebib, S. Ben Hassine, I. Boudiche, Hela Boudabous
Publikováno v:
Annales d'Endocrinologie. 81:364
Introduction Le syndrome de MEGDEL (3methylglutaconic aciduria with deafness, encephalopathy and Leigh-like) est une mitochondriopathie rare, affectant le trafic intracellulaire du cholesterol, caracterisee par un retard psychomoteur, une surdite, un
Autor:
Hatem Azzouz, Kaothar Hakim, Amel Ben Chehida, Mohamed Slim Abdelmoula, Neji Tebib, Rim Ben Abdelaziz, Mariem Oujra, Sana Ben Messaoud, Hela Boudabous, Hadhami Ben Turkia
Publikováno v:
Journal of tropical pediatrics. 65(3)
Background The outcome of Kawasaki disease (KD) depends on cardiovascular complications (CVCs). Objectives This study aimed to explore diagnostic features and CVCs in Tunisian patients with KD. Methods In total, 33 Tunisian patients (age, 2.9 ± 2.2
Autor:
Neziha Kaabachi, Zeineb Ben Ameur, Hajer Mansouri, Sonia Abdelhak, Neji Tebib, Sana Ben Messaoud, Yosra Sassi, Rim Ben Abdelaziz, Hela Boudabous, Hatem Azzouz, Amel Ben Chehida, Kaouthar Hakim, Mohamed Slim Abdelmoula, Nadia Ben Ali
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism
Journal of Pediatric Endocrinology and Metabolism, Walter de Gruyter, 2018, ⟨10.1515/jpem-2018-0151⟩
Journal of Pediatric Endocrinology and Metabolism, Walter de Gruyter, 2018, ⟨10.1515/jpem-2018-0151⟩
Background Glycogen storage disease type III (GSDIII), due to a deficiency of glycogen debrancher enzyme (GDE), is particularly frequent in Tunisia. Phenotypic particularities of Tunisian patients remain unknown. Our aim was to study complications of
Autor:
Mohamed Slim Abdelmoula, Neji Tebib, M. Ben Dridi, N. Amdouni, Hatem Azzouz, H. Ben Turkia, A. Hamzaoui, F. El Mazni
Publikováno v:
Journal des Maladies Vasculaires. 33:242-246
The pediatric forms of Wegener granulomatosis (WG) are rare. The clinical picture and the profile have specificities compared to those of adults. We report a case of a girl aged of four years and a half who presented initially with a clinical picture
Autor:
Sonia Abdelhak, Hatem Azzouz, Hela Boudabbous, Neji Tebib, Faten Ben Rehouma, Amel Ben Chehida, Mohamed Slim Abdelmoula, Rim Ben Abdelaziz, Naziha Kaabachi, Hadhami Ben Turkia, Takoua Bensmaïl
Publikováno v:
Néphrologie et Thérapeutique
Néphrologie et Thérapeutique, Elsevier Masson, 2015, 11 (4), pp.240-245. ⟨10.1016/j.nephro.2014.12.007⟩
Néphrologie et Thérapeutique, Elsevier Masson, 2015, 11 (4), pp.240-245. ⟨10.1016/j.nephro.2014.12.007⟩
International audience; Aim. - To investigate risk factors of renal complications in glycogen storage disease type I, in order to identify practical implications for renal preservation. Methods. - A retrospective study of 38 patients with glycogen st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0cbc1823ad99d56ee11477d2cb536ee
https://hal-riip.archives-ouvertes.fr/pasteur-01375033
https://hal-riip.archives-ouvertes.fr/pasteur-01375033
Autor:
Amel, Ben Chehida, Takoua, Bensmaïl, Faten, Ben Rehouma, Rim, Ben Abdelaziz, Hatem, Azzouz, Hela, Boudabbous, Mohamed, Slim Abdelmoula, Sonia, Abdelhak, Naziha, Kaabachi, Hadhami, Ben Turkia, Néji, Tebib
Publikováno v:
Nephrologietherapeutique. 11(4)
To investigate risk factors of renal complications in glycogen storage disease type I, in order to identify practical implications for renal preservation.A retrospective study of 38 patients with glycogen storage disease type I.The patients studied w