Search research articles
Contact Us
Filters
Showing results (31-40 of 84) with videos related to
Page
of 9
Sort By:
Developmental Science
|
January 14, 2005
Maladaptive conflict monitoring as evidence for executive dysfunction in children with chromosome 22q11.2 deletion syndrome
Joel P Bish, Samantha M Ferrante, Donna McDonald-McGinn, et al.
Journal of Autism and Developmental Disorders
|
September 19, 2013
Social impairments in chromosome 22q11.2 deletion syndrome (22q11.2DS): autism spectrum disorder or a different endophenotype?
Kathleen Angkustsiri, Beth Goodlin-Jones, Lesley Deprey, et al.
Psychiatry Research
|
January 16, 2010
Increased incidence and size of cavum septum pellucidum in children with chromosome 22q11.2 deletion syndrome
Elliott A Beaton, Yufeng Qin, Vy Nguyen, et al.
The Journal of Biological Chemistry
|
July 30, 2015
Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome
Eleonora Napoli, Flora Tassone, Sarah Wong, et al.
Behavioral and Brain Functions : BBF
|
June 19, 2008
Atypical cortical connectivity and visuospatial cognitive impairments are related in children with chromosome 22q11.2 deletion syndrome
Tony J Simon, Zhongle Wu, Brian Avants, et al.
Journal of Neurodevelopmental Disorders
|
March 18, 2014
Common and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes
Andrea I Quintero, Elliott A Beaton, Danielle J Harvey, et al.
Journal of Autism and Developmental Disorders
|
December 25, 2007
Brief report: methods for acquiring structural MRI data in very young children with autism without the use of sedation
Christine Wu Nordahl, Tony J Simon, Cynthia Zierhut, et al.
Neuroimage
|
April 23, 2013
White matter microstructural abnormalities in girls with chromosome 22q11.2 deletion syndrome, Fragile X or Turner syndrome as evidenced by diffusion tensor imaging
Julio Villalon-Reina, Neda Jahanshad, Elliott Beaton, et al.
Neuroimage
|
March 1, 2005
Volumetric, connective, and morphologic changes in the brains of children with chromosome 22q11.2 deletion syndrome: an integrative study
Tony J Simon, Lijun Ding, Joel P Bish, et al.
American Journal on Intellectual and Developmental Disabilities
|
May 6, 2010
Atypical functional brain activation during a multiple object tracking task in girls with Turner syndrome: neurocorrelates of reduced spatiotemporal resolution
Elliott A Beaton, Joel Stoddard, Song Lai, et al.
Page
of 9
Search research articles
Search
Showing results (31-40 of 84) with videos related to
Sort By:
Page
of 9
Developmental Science
|
January 14, 2005
Maladaptive conflict monitoring as evidence for executive dysfunction in children with chromosome 22q11.2 deletion syndrome
Joel P Bish, Samantha M Ferrante, Donna McDonald-McGinn, et al.
Journal of Autism and Developmental Disorders
|
September 19, 2013
Social impairments in chromosome 22q11.2 deletion syndrome (22q11.2DS): autism spectrum disorder or a different endophenotype?
Kathleen Angkustsiri, Beth Goodlin-Jones, Lesley Deprey, et al.
Psychiatry Research
|
January 16, 2010
Increased incidence and size of cavum septum pellucidum in children with chromosome 22q11.2 deletion syndrome
Elliott A Beaton, Yufeng Qin, Vy Nguyen, et al.
The Journal of Biological Chemistry
|
July 30, 2015
Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome
Eleonora Napoli, Flora Tassone, Sarah Wong, et al.
Behavioral and Brain Functions : BBF
|
June 19, 2008
Atypical cortical connectivity and visuospatial cognitive impairments are related in children with chromosome 22q11.2 deletion syndrome
Tony J Simon, Zhongle Wu, Brian Avants, et al.
Journal of Neurodevelopmental Disorders
|
March 18, 2014
Common and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes
Andrea I Quintero, Elliott A Beaton, Danielle J Harvey, et al.
Journal of Autism and Developmental Disorders
|
December 25, 2007
Brief report: methods for acquiring structural MRI data in very young children with autism without the use of sedation
Christine Wu Nordahl, Tony J Simon, Cynthia Zierhut, et al.
Neuroimage
|
April 23, 2013
White matter microstructural abnormalities in girls with chromosome 22q11.2 deletion syndrome, Fragile X or Turner syndrome as evidenced by diffusion tensor imaging
Julio Villalon-Reina, Neda Jahanshad, Elliott Beaton, et al.
Neuroimage
|
March 1, 2005
Volumetric, connective, and morphologic changes in the brains of children with chromosome 22q11.2 deletion syndrome: an integrative study
Tony J Simon, Lijun Ding, Joel P Bish, et al.
American Journal on Intellectual and Developmental Disabilities
|
May 6, 2010
Atypical functional brain activation during a multiple object tracking task in girls with Turner syndrome: neurocorrelates of reduced spatiotemporal resolution
Elliott A Beaton, Joel Stoddard, Song Lai, et al.
Page
of 9