Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Maherzia Ferchichi"'
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
Autor:
Neji Tebib, Sana Ben Messaoud, Hela Boudabous, Hatem Azzouz, Rim Ben Abdelaziz, Maherzia Ferchichi, Amel Ben Chehida, Henda Kachouri Chakchouk, Hela Hajji
Publikováno v:
Journal of Developmental and Physical Disabilities. 31:753-776
Limited published research has evaluated mental health in parents of children with phenylketonuria (PKU) and their coping strategies. We aimed to assess anxiety, depression and coping in parents of Tunisian children treated for PKU. We conducted a cr
Autor:
S. Rezgui, Maherzia Ferchichi, A. Ben Chehida, Hatem Azzouz, Neji Tebib, M. Ben Dridi, F.Z. Ben Salah, R. Ben Abdelaziz, H. Mansouri, H. Ben Turkia
Publikováno v:
Journal de Réadaptation Médicale : Pratique et Formation en Médecine Physique et de Réadaptation. 35:238-244
Resume But Traduire et adapter l’echelle Francaise DESS en arabe dialectal Tunisien et etudier sa validite par un pre-test sur un echantillon de personnes tunisiennes polyhandicapees (PPH). Methodes L’etude s’est deroulee en 2 etapes : (1) trad
Autor:
Taieb Messaoud, Hatem Azzouz, Naziha Kaabachi, Sonia Abdelhak, Ahlem Belhaj, Neji Tebib, Sameh Khemir, Amel Bedoui, Maherzia Ferchichi, Soumeyya Halayem, Asma Guedria, Hajer Siala
Publikováno v:
Journal of Child Neurology
Journal of Child Neurology, SAGE Publications (UK and US), 2016, 31 (7), pp.843--849. ⟨10.1177/0883073815623636⟩
Journal of Child Neurology, SAGE Publications (UK and US), 2016, 31 (7), pp.843--849. ⟨10.1177/0883073815623636⟩
Autism has been reported in untreated patients with phenylketonuria. The authors aimed to explore autism in 15 Tunisian and 4 Algerian phenylketonuria patients, and report their clinical, biochemical and molecular peculiarities. The Childhood Autism
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b1998934f9dfa1e21fc74f4bce451e0
https://hal-riip.archives-ouvertes.fr/pasteur-01469443
https://hal-riip.archives-ouvertes.fr/pasteur-01469443