Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Vivian Shyu"'
Autor:
Rajiv S. Jhangiani, Beverly Dolinsky, Eric Klein, Erin Harden, Vivian Shyu, David B. Strohmetz, Dee Posey
Publikováno v:
Scholarship of Teaching and Learning in Psychology. 1:200-207
Autor:
Bruce F. Pennington, Sally J. Rogers, Loisa Bennetto, Elizabeth McMahon Griffith, D. Taffy Reed, Vivian Shyu
This chapter aims to examine the validity of the hypothesis that executive dysfunction is the primary psychological cause of autism. It reviews work that supports this hypothesis, defines executive functions and elaborates on the executive dysfunctio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f8a03d3adebbe8ae3880d74beba87d4
https://doi.org/10.1093/med:psych/9780198523499.003.0005
https://doi.org/10.1093/med:psych/9780198523499.003.0005
Autor:
Vivian Shyu, Megan Lampe, Tracy Stackhouse, Annette K. Taylor, Randi J Hagerman, J. McGrath, Daniel N. McIntosh, K. Neitzel, Flora Tassone, Lucy Jane Miller
Publikováno v:
American Journal of Medical Genetics. 83:268-279
The fragile X mutation and fragile X syndrome are associated with hyperarousal, hyperactivity, aggression, and anxiety. These may be related to strong reactions to auditory, tactile, visual, and olfactory stimuli [Hagerman, 1996b; Hagerman and Cronis
Publikováno v:
Developmental medicine and child neurology. 41(9)
It was hypothesized that children clinically identified with sensory-modulation disruptions (SMD) would have atypical physiological responses to sensation, and that such responses would predict parent-reported behavioral responses to sensation. Ninet
Autor:
Randi J Hagerman, Vivian Shyu, Kellie A. Lugenbeel, David L. Nelson, Louise W. Staley, William E. Sobesky, Elizabeth Berry-Kravis, Annette K. Taylor, Bruce F. Pennington, Scott A. Merenstein
Publikováno v:
Journal of the American Academy of Child and Adolescent Psychiatry. 33(9)
The present case study features an adult male who was diagnosed with fragile X syndrome after the identification of this syndrome in his more affected brother. The patient presented with a Full Scale IQ within the broad range of normal and has been d