Facial emotion perception by intensity in children and adolescents with 22q11.2 deletion syndrome

Autor: Massimiliano Rossi, G. Saucourt, Jean-Yves Baudouin, Gabrielle Chesnoy, Arnaud Leleu, Caroline Demily, P. Edery, Nicolas Franck, C. Rigard

Publikováno v: European Child and Adolescent Psychiatry
European Child and Adolescent Psychiatry, Springer Verlag, 2016, 25 (3), pp.297-310. ⟨10.1007/s00787-015-0741-1⟩
European Child and Adolescent Psychiatry, Springer Verlag, 2016, 25 (3), pp.297-310. 〈http://link.springer.com/article/10.1007%2Fs00787-015-0741-1〉. 〈10.1007/s00787-015-0741-1〉
European Child and Adolescent Psychiatry, Springer Verlag (Germany), 2016, 25 (3), pp.297-310. ⟨10.1007/s00787-015-0741-1⟩

International audience; Difficulties in the recognition of emotions in expressive faces have been reported in people with 22q11.2 deletion syndrome (22q11.2DS). However, while low-intensity expressive faces are frequent in everyday life, nothing is k

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b119c6b362a5ccc9213060a01a431685
https://doi.org/10.1007/s00787-015-0741-1

[Social cognition disorders in Klinefelter syndrome: A specific phenotype? (KS)]

Autor: M-N, Babinet, C, Rigard, É, Peyroux, A-R, Dragomir, I, Plotton, H, Lejeune, C, Demily

Publikováno v: L'Encephale. 43(5)

The Klinefelter syndrome (KS) is a genetic condition characterized by an X supernumerary sex chromosome in males. The syndrome is frequently associated with cognitive impairment. Indeed, the different areas of the executive sphere can be affected suc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::936db41782332b184f2f2cf654e18092
https://pubmed.ncbi.nlm.nih.gov/27743676

[Smith-Magenis syndrome is an association of behavioral and sleep/wake circadian rhythm disorders]

Autor: A, Poisson, A, Nicolas, D, Sanlaville, P, Cochat, H, De Leersnyder, C, Rigard, P, Franco, V, des Portes, P, Edery, C, Demily

Publikováno v: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 22(6)

Smith-Magenis syndrome (SMS) is a genetic disorder characterized by the association of facial dysmorphism, oral speech delay, as well as behavioral and sleep/wake circadian rhythm disorders. Most SMS cases (90%) are due to a 17p11.2 deletion encompas

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::187062406251303eb2d5f5c5fa6c5c92
https://pubmed.ncbi.nlm.nih.gov/25934608

Pertinence d’un groupe d’affirmation de soi pour des personnes porteuses d’une délétion 22q11.2

Autor: D’Amato, I. Seguin, C. Rigard, C. Demily

Publikováno v: European Psychiatry. 28:24-25

L’affirmation de soi fait partie des techniques d’orientation cognitivo-comportementale visant à développer les aptitudes nécessaires pour communiquer de façon adaptée, en tenant compte des codes sociaux consensuels. Elle permet de prévaloi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::cc08e87c46ca865c617bb95481b0c031
https://doi.org/10.1016/j.eurpsy.2013.09.060

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