Networks of attention in children with the 22q11 deletion syndrome. - Wikidata - awgldk - TriplyDB

Networks of attention in children with the 22q11 deletion syndrome.

Networks of attention in children with the 22q11 deletion syndrome.

http://www.wikidata.org/entity/Q37365844

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Effects of painful stimulation and acupuncture on attention networks in healthy subjects Corpus callosum morphology and ventricular size in chromosome 22q11.2 deletion syndrome Subjective experience of episodic memory and metacognition: a neurodevelopmental approach Behavioral and Psychiatric Phenotypes in 22q11.2 Deletion Syndrome Haploinsufficiency of the 22q11.2 microdeletion gene Mrpl40 disrupts short-term synaptic plasticity and working memory through dysregulation of mitochondrial calcium.Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders.22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.Associations between prepulse inhibition and executive visual attention in children with the 22q11 deletion syndrome Lower prepulse inhibition in children with the 22q11 deletion syndrome.Cognitive characteristics of children with genetic syndromes.Velo-Cardio-Facial Syndrome.Children with chromosome 22q11.2 deletion syndrome exhibit impaired spatial working memory.Selective impairments of alerting and executive control in HIV-infected patients: evidence from attention network test.Increased incidence and size of cavum septum pellucidum in children with chromosome 22q11.2 deletion syndrome.A multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children.Atypical development of the executive attention network in children with chromosome 22q11.2 deletion syndrome Deficiency of Dgcr8, a gene disrupted by the 22q11.2 microdeletion, results in altered short-term plasticity in the prefrontal cortex.Mapping cortical morphology in youth with velocardiofacial (22q11.2 deletion) syndrome.Neurocognitive development in 22q11.2 deletion syndrome: comparison with youth having developmental delay and medical comorbidities.The neural correlates of non-spatial working memory in velocardiofacial syndrome (22q11.2 deletion syndrome)The hippocampi of children with chromosome 22q11.2 deletion syndrome have localized anterior alterations that predict severity of anxiety.A gender-moderated effect of a functional COMT polymorphism on prefrontal brain morphology and function in velo-cardio-facial syndrome (22q11.2 deletion syndrome).Domain specific attentional impairments in children with chromosome 22q11.2 deletion syndrome.Neuromotor deficits in children with the 22q11 deletion syndrome.Social skills and executive function deficits in children with the 22q11 Deletion Syndrome.Common and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes.Cognitive Translation Using the Rodent Touchscreen Testing Approach.Potential Role of Cortisol in Social and Memory Impairments in Individuals with 22q11.2 Deletion Syndrome.Attentional network deficits in children with autism spectrum disorder.Executive functions and memory abilities in children with 22q11.2 deletion syndrome.LINE-1 Retrotransposons in Healthy and Diseased Human Brain.Time-based prospective memory in children and adolescents with 22q11.2 deletion syndrome.Does differential visual exploration contribute to visual memory impairments in 22q11.2 microdeletion syndrome?Continuous performance test impairment in a 22q11.2 microdeletion mouse model: improvement by amphetamine

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P2860

Networks of attention in children with the 22q11 deletion syndrome.

http://www.wikidata.org/entity/Q37365844

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on January 2004

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Networks of attention in children with the 22q11 deletion syndrome.

@en

Networks of attention in children with the 22q11 deletion syndrome.

@nl

type

label

Networks of attention in children with the 22q11 deletion syndrome.

@en

Networks of attention in children with the 22q11 deletion syndrome.

@nl

prefLabel

Networks of attention in children with the 22q11 deletion syndrome.

@en

Networks of attention in children with the 22q11 deletion syndrome.

@nl

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Developmental Neuropsychology

P1476

Networks of attention in children with the 22q11 deletion syndrome.

@en

P2093

Christina Sobin

http://www.w3.org/2001/XMLSchema#string

Karen Kiley-Brabeck

http://www.w3.org/2001/XMLSchema#string

Maria Karayiorgou

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Maude Blundell

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Sarah Daniels

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P2860

Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior.

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

Increased activity in human visual cortex during directed attention in the absence of visual stimulation

Testing the efficiency and independence of attentional networks

A common network of functional areas for attention and eye movements

Parallel Organization of Functionally Segregated Circuits Linking Basal Ganglia and Cortex

Velocardiofacial (Shprintzen) syndrome: an important syndrome for the dysmorphologist to recognise.

Prevalence of 22q11 microdeletion.

Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS.

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

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611-626

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scholarly article

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10.1207/S15326942DN2602_5

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2

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26

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Kwame Anyane-Yeboa

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2004-01-01T00:00:00Z

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8258217

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15456687

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2753367

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