Zobrazeno 1 - 10
of 34
pro vyhledávání: '"DÉCIO BRUNONI"'
Autor:
Daniela Bordini, Ana Cláudia Moya, Graccielle Rodrigues da Cunha Asevedo, Cristiane Silvestre Paula, Décio Brunoni, Helena Brentani, Sheila Cavalcante Caetano, Jair de Jesus Mari, Leila Bagaiolo
Publikováno v:
Brain Sciences, Vol 14, Iss 2, p 172 (2024)
Social communication skills, especially eye contact and joint attention, are frequently impaired in autism spectrum disorder (ASD) and predict functional outcomes. Applied behavior analysis is one of the most common evidence-based treatments for ASD,
Externí odkaz:
https://doaj.org/article/9b742622144c465e8f65257f42ace8c6
Autor:
Fábio Pinato Sato, Cristiane Silvestre Paula, Rosane Lowenthal, Eduardo Yoshio Nakano, Décio Brunoni, José Salomão Schwartzman, Marcos Tomanik Mercadante
Publikováno v:
Brazilian Journal of Psychiatry, Vol 31, Iss 1, Pp 30-33 (2009)
OBJECTIVE: To translate into Portuguese, back-translate, culturally adapt and validate a screening instrument for pervasive developmental disorder, the Autism Screening Questionnaire, for use in Brazil. METHOD: A sample of 120 patients was selected b
Externí odkaz:
https://doaj.org/article/9f806eb65590440c83ebe54d62afb9f5
Autor:
Fernanda T. Orsati, José Salomão Schwartzman, Décio Brunoni, Tatiana Mecca, Elizeu C. de Macedo
Publikováno v:
Avaliação Psicológica, Vol 7, Iss 3, Pp 281-290 (2008)
O presente trabalho teve por objetivo utilizar o rastreamento ocular como parte da avaliação neuropsicológica em crianças e jovens com TID. Foram avaliadas 10 crianças e jovens com diagnóstico clínico de TID, idade média 11,9 (DP=3,22). Todas
Externí odkaz:
https://doaj.org/article/2b856f53d4244decaaa8c464e8ef130c
Autor:
Denise M. Christofolini, Monica V.N. Lipay, Marco Antonio P. Ramos, Silvia S. Costa, Fernanda T.S. Bellucco, Sintia I. Nogueira, Leslie D. Kulikowski, Décio Brunoni, Maria Isabel Melaragno
Publikováno v:
Genetics and Molecular Biology, Vol 30, Iss 4, Pp 1047-1050 (2007)
Fragile X syndrome is the most frequent cause of inherited mental retardation. The phenotype in this syndrome is quite variable and less conspicuous in younger patients, making clinical diagnosis difficult and thus making molecular diagnosis necessar
Externí odkaz:
https://doaj.org/article/c0cf83b0ca304c2cb0b6f0727ed7efdd
Publikováno v:
Brazilian Journal of Psychiatry, Vol 26, Iss 4, Pp 270-272 (2004)
O autismo é uma doença neuropsiquiátrica com profundas conseqüências sociofamilares. Inúmeros trabalhos investigaram pacientes e famílias com metodologia genético-clínica, citogenética e biologia molecular. Os resultados destes trabalhos ap
Externí odkaz:
https://doaj.org/article/d528f71d22744933bf54e2d8569e630a
Publikováno v:
Genetics and Molecular Biology, Vol 23, Iss 1, Pp 25-27 (2000)
We studied 228 patients, with suspected or confirmed genetic hearing loss, in order to determine the clinical and genetic diagnoses and etiology of each case. Deafness with no associated abnormalities was found in 146 patients (64%) belonging to 112
Externí odkaz:
https://doaj.org/article/8d31ebd88b9f428dad7923f757c3c21c
Autor:
Maria Cristina Triguero Veloz Teixeira, Décio Brunoni, Luiz Renato Rodrigues Carreiro, Ana Claudia Braga, Naiara Adorna da Silva, Cristiane Silvestre Paula
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 75, Iss 4, Pp 244-247
ABSTRACT Objective To assess the diagnostic status, the sociodemographic and health profiles for students with special educational needs (SEN) in a public educational system, and to map their use of educational/social services. Methods The sample com
Externí odkaz:
https://doaj.org/article/6622c2adb38b4b95a9292da8d8bc64f7
Autor:
Banny Silva Barbosa Correia, João Guilherme de Moraes Pontes, João Victor Silva Nani, Fabian Villalta, Natalia Cristina Mor, Daniela Bordini, Décio Brunoni, Helena Brentani, Jair Jesus Mari, Mirian A. F. Hayashi, Ljubica Tasic
Publikováno v:
ACS Chemical Neuroscience. 14:1137-1145
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b75653ba3dde00b8a4555c1a52cdb61
https://doi.org/10.1021/acschemneuro.2c00735
https://doi.org/10.1021/acschemneuro.2c00735
Autor:
Keila Cristina Leme dos Santos Coelho, JANAÍNA APARECIDA DE OLIVEIRA AUGUSTO, MARIA ELOISA FAMÁ D'ANTINO, DÉCIO BRUNONI, NATÁLIA BECKER
Publikováno v:
Anais do IV Congresso Brasileiro de Saúde On-line.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42e84a74a3e75c2b50caa105e4d6f6ae
https://doi.org/10.51161/conbrasau2023/18644
https://doi.org/10.51161/conbrasau2023/18644
Autor:
Ariadne R. Lima, Barbara M. Ferreira, Chaofan Zhang, Angad Jolly, Haowei Du, Janson J. White, Moez Dawood, Tulio C. Lins, Marcela A. Chiabai, Ellen van Beusekom, Mara S. Cordoba, Erica C.C. Caldas Rosa, Hulya Kayserili, Virginia Kimonis, Erica Wu, Cecilia Mellado, Vineet Aggarwal, Antonio Richieri‐Costa, Décio Brunoni, Talyta M. Canó, Alexander A. L. Jorge, Chong A. Kim, Rachel Honjo, Débora R. Bertola, Raissa M. Dandalo‐Girardi, Yavuz Bayram, Alper Gezdirici, Elif Yilmaz‐Gulec, Evren Gumus, Gülay C. Yilmaz, Nobuhiko Okamoto, Hirofumi Ohashi, Zeynep Coban–Akdemir, Tadahiro Mitani, Shalini N. Jhangiani, Donna M. Muzny, Neysa A.P. Regattieri, Robert Pogue, Rinaldo W. Pereira, Paulo A. Otto, Richard A. Gibbs, Bassam R. Ali, Hans van Bokhoven, Han G. Brunner, V. Reid Sutton, James R. Lupski, Angela M. Vianna‐Morgante, Claudia M. B. Carvalho, Juliana F. Mazzeu
Publikováno v:
Human Mutation. 43
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15fd5514ce85befcf36271a353fe1db8
https://doi.org/10.1002/humu.24420
https://doi.org/10.1002/humu.24420