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Trends in Neurosciences|May 14, 1999
Bridging cognition, the brain and molecular genetics: evidence from Williams syndromeU Bellugi, L Lichtenberger, D Mills, et al.Brain and Language|January 1, 1993
Dissociation of cortical and single unit activity in spoken and signed languagesM M Haglund, G A Ojemann, E Lettich, et al.Journal of Cognitive Neuroscience|August 23, 2000
I. The neurocognitive profile of Williams Syndrome: a complex pattern of strengths and weaknessesU Bellugi, L Lichtenberger, W Jones, et al.Annals of Neurology|August 1, 1989
Abnormal pattern electroretinogram in Alzheimer's disease: evidence for retinal ganglion cell degeneration?B Katz, S Rimmer, V Iragui, et al.Archives of Neurology|February 1, 1993
Cerebral morphologic distinctions between Williams and Down syndromesT L Jernigan, U Bellugi, E Sowell, et al.Investigative Ophthalmology & Visual Science|September 1, 1989
Retinocortical time exhibits spatial selectivityS Rimmer, V Iragui, M R Klauber, et al.Journal of Cognitive Neuroscience|August 22, 2013
Is there a social module? Language, face processing, and theory of mind in individuals with williams syndromeA Karmiloff-Smith, E Klima, U Bellugi, et al.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.Pageof 12