I. The neurocognitive profile of Williams Syndrome: a complex pattern of strengths and weaknesses.
about
Rethinking the concepts of 'local or global processors': evidence from Williams syndrome, Down syndrome, and Autism Spectrum DisordersA human neurodevelopmental model for Williams syndromeWilliams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23Cortical Folding of the Primate Brain: An Interdisciplinary Examination of the Genetic Architecture, Modularity, and Evolvability of a Significant Neurological Trait in Pedigreed Baboons (Genus Papio)Pitch Processing in Children with Williams Syndrome: Relationships between Music and Prosody Skills.(A)musicality in Williams syndrome: examining relationships among auditory perception, musical skill, and emotional responsiveness to music.Social functioning and autonomic nervous system sensitivity across vocal and musical emotion in Williams syndrome and autism spectrum disorder.Cross-modal influences of affect across social and non-social domains in individuals with Williams syndrome.Sensitivity of the autonomic nervous system to visual and auditory affect across social and non-social domains in williams syndromeAtypical hemispheric asymmetry in the perception of negative human vocalizations in individuals with Williams syndrome.Visual phenotype in Williams-Beuren syndrome challenges magnocellular theories explaining human neurodevelopmental visual cortical disordersWhat developmental disorders can tell us about the nature and origins of language.Induced chromosome deletion in a Williams-Beuren syndrome mouse model causes cardiovascular abnormalities.The effect of intellectual ability on functional activation in a neurodevelopmental disorder: preliminary evidence from multiple fMRI studies in Williams syndrome3D pattern of brain abnormalities in Williams syndrome visualized using tensor-based morphometry.Research Review: Williams syndrome: a critical review of the cognitive, behavioral, and neuroanatomical phenotype.Do individuals with Williams syndrome possess absolute pitch?Absolute pitch memory: its prevalence among musicians and dependence on the testing context.Electrophysiological studies of face processing in developmental prosopagnosia: neuropsychological and neurodevelopmental perspectives.The role of domain-general cognitive control in language comprehensionNeural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour.Cognitive characteristics of children with genetic syndromes.Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior.Exploring empathic space: correlates of perspective transformation ability and biases in spatial attentionMolecular dissection of DNA sequences and factors involved in slow muscle-specific transcription.Morphometry of human insular cortex and insular volume reduction in Williams syndrome.Abnormal structure or function of the amygdala is a common component of neurodevelopmental disorders.Toward a deeper characterization of the social phenotype of Williams syndrome: The association between personality and social driveAffiliative behavior in Williams syndrome: social perception and real-life social behaviorEnhanced prefrontal serotonin 5-HT(1A) currents in a mouse model of Williams-Beuren syndrome with low innate anxiety.Optogenetic insights on the relationship between anxiety-related behaviors and social deficits.Genetic contributions to visuospatial cognition in Williams syndrome: insights from two contrasting partial deletion patientsRearrangements of the Williams-Beuren syndrome locus: molecular basis and implications for speech and language development.Face processing improvements in prosopagnosia: successes and failures over the last 50 yearsNature and nurture: Williams syndrome across cultures.Global analysis of gene expression in the developing brain of Gtf2ird1 knockout mice.Longitudinal course of anxiety in children and adolescents with Williams syndromeAutistic disorder in patients with Williams-Beuren syndrome: a reconsideration of the Williams-Beuren syndrome phenotype.A direct comparison of local-global integration in autism and other developmental disorders: implications for the central coherence hypothesis.An atypical 7q11.23 deletion in a normal IQ Williams-Beuren syndrome patient.
P2860
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P2860
I. The neurocognitive profile of Williams Syndrome: a complex pattern of strengths and weaknesses.
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2000 nî lūn-bûn
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2000 թվականի հունվարին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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2000年論文
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2000年論文
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I. The neurocognitive profile ...... n of strengths and weaknesses.
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I. The neurocognitive profile ...... n of strengths and weaknesses.
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I. The neurocognitive profile ...... n of strengths and weaknesses.
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I. The neurocognitive profile ...... n of strengths and weaknesses.
@ast
I. The neurocognitive profile ...... n of strengths and weaknesses.
@en
I. The neurocognitive profile ...... n of strengths and weaknesses.
@nl
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I. The neurocognitive profile ...... n of strengths and weaknesses.
@ast
I. The neurocognitive profile ...... n of strengths and weaknesses.
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I. The neurocognitive profile ...... n of strengths and weaknesses.
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P2093
P2860
P356
P1476
I. The neurocognitive profile ...... n of strengths and weaknesses.
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P2093
P2860
P356
10.1162/089892900561959
P478
12 Suppl 1
P577
2000-01-01T00:00:00Z