Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Charles Bouis"'
Autor:
Cécile Cieuta-Walti, Aude Pichot, Jennifer Gallard, Silvia Sacco, Isabelle Marey, Clotilde Mircher, Elodie Blondiaux, Franck Sturtz, Aimé Ravel, Charles Bouis, Nathalie Dorison
Publikováno v:
American Journal of Medical Genetics Part A. 188:818-827
Children with Down syndrome (DS) show delayed acquisition of cognitive and functional skills compared to typically developing children. The objective of this study was to accurately describe early development of infants and young children (children h
Autor:
Charles Bouis
Publikováno v:
Contraste. :155-164
La redaction de ce temoignage sur le metier de neuropsychologue m’a fait prendre conscience du fait que cela faisait deja presque quinze ans que je travaillais aupres d’enfants et d’adolescents ayant des besoins specifiques d’accompagnement.
Autor:
Charles Bouis, Jean Dewailly, Ahlam Azar-Kolakez, Rosa-Maria Guéant-Rodriguez, Isabelle Marey, Oliver Greiner-Mahler, Jean-Louis Guéant, Aude Pichot, Samantha Stora, Silvia Sacco, Dominique Bonnefont-Rousselot, Emilie Schlumberger, Franck Sturtz, Eric Le Galloudec, Nathalie Dorison, Clotilde Mircher, Elodie Blondiaux, Alicia Gambarini, André Baruchel, Sophie Durand, Jennifer Gallard, Aimé Ravel, Didier Borderie, Michel Polak, Cécile Cieuta
Publikováno v:
Yearbook of Paediatric Endocrinology.
To determine whether folinic acid (FA) and thyroxine, in combination or alone, benefit psychomotor development in young patients with Down syndrome (DS). The Assessment of Systematic Treatment With Folinic Acid and Thyroid Hormone on Psychomotor Deve
Publikováno v:
Revue de neuropsychologie. 3:155
Differentes etudes montrent que l’epilepsie peut interferer avec le developpement cognitif, moteur, mais aussi comportemental du patient. La plupart des travaux se sont donc interesses a l’evaluation de l’efficience intellectuelle, du fonctionn
Autor:
Charles Bouis, Isabelle Jambaqué, Rima Nabbout, Dorothée Leunen, Mathilde Chipaux, Celia Dubouch, Olivier Dulac, Giulia Barcia, Nicole Chemaly, Catherine Chiron, Georges Dellatolas
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, 2013, 8 (1), pp.176. ⟨10.1186/1750-1172-8-176⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2013, 8 (1), pp.176. 〈10.1186/1750-1172-8-176〉
Orphanet Journal of Rare Diseases, BioMed Central, 2013, 8 (1), pp.176. ⟨10.1186/1750-1172-8-176⟩
Orphanet Journal of Rare Diseases, 2013, 8 (1), pp.176. ⟨10.1186/1750-1172-8-176⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2013, 8 (1), pp.176. 〈10.1186/1750-1172-8-176〉
Orphanet Journal of Rare Diseases, BioMed Central, 2013, 8 (1), pp.176. ⟨10.1186/1750-1172-8-176⟩
International audience; BACKGROUND: Dravet syndrome (DS) is currently considered as an epileptic encephalopathy, a condition in which epilepsy causes deterioration or developmental delay but preliminary data suggested that cognitive course may worsen