Showing results (151-160 of 164) with videos related to
Sort By:
Pageof 17
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|August 6, 2010
Cross-linguistic neuroimaging and dyslexia: a critical viewTarik Hadzibeganovic, Maurits van den Noort, Peggy Bosch, et al.Journal of the International Neuropsychological Society : JINS|April 12, 2017
Atypical Local Interference Affects Global Processing in Children with Neurofibromatosis Type 1Jonathan M Payne, Melanie A Porter, Samantha Bzishvili, et al.Cerebral Cortex (New York, N.Y. : 1991)|January 6, 2004
Enlarged temporal lobes in Turner syndrome: an X-chromosome effect?Caroline Rae, Pamela Joy, Jenny Harasty, et al.Frontiers in Human Neuroscience|July 5, 2014
Using hypnosis to disrupt face processing: mirrored-self misidentification delusion and different visual mediaMichael H Connors, Amanda J Barnier, Max Coltheart, et al.Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|February 20, 2018
Belief, delusion, hypnosis, and the right dorsolateral prefrontal cortex: A transcranial magnetic stimulation studyMax Coltheart, Rochelle Cox, Paul Sowman, et al.Research in Developmental Disabilities|November 2, 2013
Gait profiles as indicators of domain-specific impairments in executive control across neurodevelopmental disordersDarren R Hocking, Jasmine C Menant, Hannah E Kirk, et al.Journal of Affective Disorders|November 18, 2011
A meta-analysis of cognitive deficits in first-episode Major Depressive DisorderRico S C Lee, Daniel F Hermens, Melanie A Porter, et al.Developmental Medicine and Child Neurology|June 7, 2018
Attention to faces in social context in children with neurofibromatosis type 1Amelia K Lewis, Melanie A Porter, Tracey A Williams, et al.Plos One|November 3, 2012
A role for transcription factor GTF2IRD2 in executive function in Williams-Beuren syndromeMelanie A Porter, Carol Dobson-Stone, John B J Kwok, et al.Neuropsychology|March 21, 2017
Facial emotion recognition, face scan paths, and face perception in children with neurofibromatosis type 1Amelia K Lewis, Melanie A Porter, Tracey A Williams, et al.Pageof 17