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U Bellugi

Showing results (51-60 of 71) with videos related to

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Developmental Medicine and Child Neurology|March 27, 2001
Corpus callosum morphology of Williams syndrome: relation to genetics and behaviorJ E Schmitt, S Eliez, I S Warsofsky, et al.
Journal of Psychiatric Research|October 2, 2001
Enlarged cerebellar vermis in Williams syndromeJ E Schmitt, S Eliez, I S Warsofsky, et al.
Brain and Language|April 7, 1999
Discourse deficits following right hemisphere damage in deaf signersG Hickok, M Wilson, K Clark, et al.
Neurology|October 1, 1992
Specific neurobehavioral profile of Williams' syndrome is associated with neocerebellar hemispheric preservationP P Wang, J R Hesselink, T L Jernigan, et al.
Journal of Cognitive Neuroscience|August 23, 2000
II. Hypersociability in Williams SyndromeW Jones, U Bellugi, Z Lai, et al.
Revista De Neurologia|February 25, 2003
[Williams syndrome. A summary of cognitive, electrophysiological, anatomofunctional, microanatomical and genetic findings]A M Galaburda, D Holinger, D Mills, et al.
Brain and Language|October 1, 1992
Dissociation between linguistic and nonlinguistic gestural systems: a case for compositionalityD P Corina, H Poizner, U Bellugi, et al.
Neurology|June 9, 2004
Anomalous brain activation during face and gaze processing in Williams syndromeD Mobbs, A S Garrett, V Menon, et al.
Neuropsychologia|April 1, 1992
Acquisition of signs from American sign language in hearing individuals following left hemisphere damage and aphasiaS W Anderson, H Damasio, A R Damasio, et al.
Genes, Brain, and Behavior|September 24, 2011
Preliminary evidence of abnormal white matter related to the fusiform gyrus in Williams syndrome: a diffusion tensor imaging tractography studyB W Haas, F Hoeft, N Barnea-Goraly, et al.
Pageof 8

Showing results (51-60 of 71) with videos related to

Sort By:
Pageof 8
Developmental Medicine and Child Neurology|March 27, 2001
Corpus callosum morphology of Williams syndrome: relation to genetics and behaviorJ E Schmitt, S Eliez, I S Warsofsky, et al.
Journal of Psychiatric Research|October 2, 2001
Enlarged cerebellar vermis in Williams syndromeJ E Schmitt, S Eliez, I S Warsofsky, et al.
Brain and Language|April 7, 1999
Discourse deficits following right hemisphere damage in deaf signersG Hickok, M Wilson, K Clark, et al.
Neurology|October 1, 1992
Specific neurobehavioral profile of Williams' syndrome is associated with neocerebellar hemispheric preservationP P Wang, J R Hesselink, T L Jernigan, et al.
Journal of Cognitive Neuroscience|August 23, 2000
II. Hypersociability in Williams SyndromeW Jones, U Bellugi, Z Lai, et al.
Revista De Neurologia|February 25, 2003
[Williams syndrome. A summary of cognitive, electrophysiological, anatomofunctional, microanatomical and genetic findings]A M Galaburda, D Holinger, D Mills, et al.
Brain and Language|October 1, 1992
Dissociation between linguistic and nonlinguistic gestural systems: a case for compositionalityD P Corina, H Poizner, U Bellugi, et al.
Neurology|June 9, 2004
Anomalous brain activation during face and gaze processing in Williams syndromeD Mobbs, A S Garrett, V Menon, et al.
Neuropsychologia|April 1, 1992
Acquisition of signs from American sign language in hearing individuals following left hemisphere damage and aphasiaS W Anderson, H Damasio, A R Damasio, et al.
Genes, Brain, and Behavior|September 24, 2011
Preliminary evidence of abnormal white matter related to the fusiform gyrus in Williams syndrome: a diffusion tensor imaging tractography studyB W Haas, F Hoeft, N Barnea-Goraly, et al.
Pageof 8