Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Faye van der Fluit"'
Autor:
Bonita P. Klein-Tasman, Alina M. Colon, Natalie Brei, Faye van der Fluit, Christina L. Casnar, Kelly M. Janke, Donald Basel, Dawn H. Siegel, Jasmine A. Walker
Publikováno v:
International Journal of Pediatrics, Vol 2013 (2013)
Neurofibromatosis-1 is the most common single gene disorder affecting 1 in 3000. In children, it is associated not only with physical features but also with attention and learning problems. Research has identified a downward shift in intellectual fun
Externí odkaz:
https://doaj.org/article/0dedb7fcd5f040218b665dc25a699e3f
Publikováno v:
Journal of autism and developmental disorders. 48(9)
To characterize autism spectrum-related symptomatology in children with Williams syndrome (WS) with phrase speech or fluent language, the Autism Diagnostic Observation Schedule (Lord et al., 1999) Module 2 or 3 was administered. The cutoff for autism
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b17411e8599e3d5e00fb3ff7c7c254e
https://pubmed.ncbi.nlm.nih.gov/29671106
https://pubmed.ncbi.nlm.nih.gov/29671106
Publikováno v:
Encyclopedia of Clinical Neuropsychology ISBN: 9783319567822
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::552497bc3727648bf4e2ae5d7c0a877b
https://doi.org/10.1007/978-3-319-57111-9_1609
https://doi.org/10.1007/978-3-319-57111-9_1609
Publikováno v:
Journal of Developmental and Physical Disabilities. 27:111-118
A variety of genetic disorders of known etiology present with behavioral profiles similar to that described in autism spectrum disorders (ASDs). Although some of these disorders are more likely to be associated with a comorbid ASD diagnosis, there ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::072eafac600238616e8894f2624447a8
https://doi.org/10.1007/s10882-014-9404-2
https://doi.org/10.1007/s10882-014-9404-2
Autor:
Christy L. Casnar, Bonita P. Klein-Tasman, Scott J. Hunter, Kelly M. Janke, Pamela Trapane, Lorri A. Kais, Faye van der Fluit, James H. Tonsgard, Wen Luo
Publikováno v:
Journal of the International Neuropsychological Society. 20:88-98
Children with neurofibromatosis-1 (NF1), a neurodevelopmental disorder resulting from a mutation of the NF1 gene (17q11.2), often have difficulties with learning and attention, but there is little research in the early childhood years. In this study,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::570409d677f1b903f4261290a5c26d81
https://doi.org/10.1017/s1355617713001227
https://doi.org/10.1017/s1355617713001227
Autor:
Laura J. Ely, Douglas W. Woods, Michael R. Walther, Ivar Snorrason, Flint M. Espil, Faye van der Fluit, Emily J. Ricketts, Matthew R. Capriotti, Christopher C. Bauer
Publikováno v:
Cognitive and Behavioral Practice. 20:544-555
Stereotypic movement disorder (SMD) is characterized by repetitive, rhythmic, episodic movement and is associated with distress and functional impairment. A range of behavioral strategies have been implemented for the treatment of stereotypies, but r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4cd1a99be7d6058cae4ae078acaafcb1
https://doi.org/10.1016/j.cbpra.2013.03.002
https://doi.org/10.1016/j.cbpra.2013.03.002
Autor:
Natalie G. Brei, Dawn H. Siegel, Kelly M. Janke, Jasmine A. Walker, Faye van der Fluit, Donald Basel, Bonita P. Klein-Tasman, Christina L. Casnar, Alina M. Colon
Publikováno v:
International Journal of Pediatrics
International Journal of Pediatrics, Vol 2013 (2013)
International Journal of Pediatrics, Vol 2013 (2013)
Neurofibromatosis-1 is the most common single gene disorder affecting 1 in 3000. In children, it is associated not only with physical features but also with attention and learning problems. Research has identified a downward shift in intellectual fun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cffedec1cb9df0857f27f4068f168ac
https://doi.org/10.1155/2013/690432
https://doi.org/10.1155/2013/690432
Autor:
Natalie G. Brei, Faye van der Fluit, Christy L. Casnar, Bonita P. Klein-Tasman, Kelly M. Janke
Publikováno v:
Journal of clinical and experimental neuropsychology. 36(9)
Neurofibromatosis type 1 (NF1) is one of the most common genetic disorders presenting in approximately 1 in 3,500 live births. NF1 is a highly variable condition with a large number of complications. A common complication is neuropsychological proble
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ecbd8c55a6e75c653c8f7661198331c
https://pubmed.ncbi.nlm.nih.gov/25284746
https://pubmed.ncbi.nlm.nih.gov/25284746
Publikováno v:
Frontiers in Psychology, Vol 3 (2012)
Frontiers in Psychology
Frontiers in Psychology
Williams syndrome (WS) is a developmental disorder of genetic origin, with characteristic cognitive and personality profiles. Studies of WS point to an outgoing and gregarious personality style, often contrasted with autism spectrum disorders; howeve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51144538cb0557a4b57e58278495b5cb
https://doi.org/10.3389/fpsyg.2012.00197
https://doi.org/10.3389/fpsyg.2012.00197
Publikováno v:
Encyclopedia of Autism Spectrum Disorders ISBN: 9781461464358
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32f004b333f9eadeaf3fdd867df3cb0d
https://doi.org/10.1007/978-0-387-79948-3_1609
https://doi.org/10.1007/978-0-387-79948-3_1609