Zobrazeno 1 - 10
of 257
pro vyhledávání: '"N. Touil"'
Autor:
N. Touil, B. Riche, V. Des Portes, S. Mardirossian, S. Gaillard, M. Rabilloud, B. Kassai, S. Sonie
Publikováno v:
European Psychiatry, Vol 64, Pp S155-S156 (2021)
Introduction For populations with intellectual disability and autism spectrum disorder, it is essential to complete cognitive assessment with an adaptive behavior scale. Objectives To translate VABS-II from English to French and establish norms for
Externí odkaz:
https://doaj.org/article/985913f5bb874d6483590ed641badc31
Autor:
N. Touil, A. Curie, M.-P. Reymond, F. Subtil, S. Roche, S. Gaillard, B. Kassai, V. Des Portes
Publikováno v:
European Psychiatry, Vol 64, Pp S125-S126 (2021)
Introduction There is a lack of objective evaluation with validated tools in school children with intellectual disability (ID). Standardized and validated tools, allowing children evaluations and follow-up, exist but are poorly used. Our action-study
Externí odkaz:
https://doaj.org/article/dfd6283d08724b898fd747cc7e084b25
Autor:
S. Marignier, N. Touil, F. Subtil, M. El Jani, S. Mardirossian, S. Gaillard, B. Kassai, S. Sonie
Publikováno v:
European Psychiatry, Vol 64, Pp S155-S155 (2021)
Introduction Early screening of children at-risk to develop Autism Spectrum Disorder (ASD) needs to be improved to propose early interventions. This detection should allow diagnosis of ASD before the age of 3. An early screening performed at the gene
Externí odkaz:
https://doaj.org/article/295bd36579f340a399e09f31b18198e0
Publikováno v:
Journal of Basic and Applied Zoology, Vol 66, Iss 4, Pp 164-168 (2013)
The equine influenza (EI) is a highly contagious respiratory viral disease of equines. The aim of the present study was to determine the amino acid mutation sequences of the partial nucleoprotein (NP), which includes four epitopes of the equine leuco
Externí odkaz:
https://doaj.org/article/f70a9a1132b6416ba6b1148cb1fe7ae3
Autor:
A. Jadib, D. Bentaleb, L.C. El Ouazzani, H. Tabakh, K. El Hattabi, E. Choukri, I. El Bejjaj, N.G. Bennani, A. Siwane, N. Touil, O. Kacimi, N. Chikhaoui, M. Bouali, A. Bakouri, F.Z. Bensardi, A. Fadil
Publikováno v:
Journal d'imagerie diagnostique et interventionnelle. 6:213-217
Autor:
R. Benmansour, M. R. Tagajdid, S. Elkochri, R. Aabi, H. Elannaz, A. Laraqui, B. El Mchichi, N. Touil, K. Ennibi, I. Lahlou Amine
Publikováno v:
Saudi Journal of Pathology and Microbiology. 8:90-98
Host genetics of COVID-19 patients is constantly evolving and may play an important role in the management of hospitalized patients and the identification of new biomarkers. In 2022, numerous studies have been published examining genetic factors that
Publikováno v:
Scholars Journal of Medical Case Reports. 11:291-294
Aims: Show the importance of imaging in the diagnosis and follow up of Hepar Lobatum Carcinomatosum (HLC) in the context of a breast neoplasia. Presentation of case: We report a case of an episode of upper GI hemorrhage, in a 54 year old female patie
Publikováno v:
Scholars Journal of Medical Case Reports. 11:268-272
Purpose: This case report aims to discuss the rare occurrence of spontaneous splenic rupture and the utility of CT scans in its diagnosis and management. Presentation of Case: A 58-year-old chronic smoker presented to the emergency department with su
Publikováno v:
Scholars Journal of Medical Case Reports. 11:688-690
Hydatid disease is a parasitic infection characterized by the formation of cysts in the organs. The liver and the lungs are most often affected. Cysticercosis of the spleen is rare, accounting for less than 8% of all cases of cysticercosis in humans.
Publikováno v:
EAS Journal of Radiology and Imaging Technology. 4:139-142
Bertolotti syndrome is a congenital spinal anomaly characterized by an abnormal enlargement of one or both transverse processes (mega-apophysis) of the most caudal lumbar vertebrae that articles or fuses with the sacrum and/or iliac bone resulting in