Pre-pulse inhibition and antisaccade performance indicate impaired attention modulation of cognitive inhibition in 22q11.2 deletion syndrome (22q11DS)

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1866-1955

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Pre-pulse inhibition and antisaccade performance indicate impaired attention modulation of cognitive inhibition in 22q11.2 deletion syndrome (22q11DS) ; volume:6 ; number:1 ; day:19 ; month:9 ; year:2014 ; pages:1-8 ; date:12.2014
Journal of neurodevelopmental disorders ; 6, Heft 1 (19.9.2014), 1-8, 12.2014

Creator: McCabe, Kathryn Louise

Contributor: Atkinson, Rebbekah Josephine
Cooper, Gavin
Melville, Jessica Lauren
Harris, Jill
Schall, Ulrich
Loughland, Carmel Maree
Thienel, Renate
Campbell, Linda Elisabet
SpringerLink (Online service)

DOI: 10.1186/1866-1955-6-38

URN: urn:nbn:de:1111-2016021613480

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:23 AM CEST

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Associated

McCabe, Kathryn Louise
Atkinson, Rebbekah Josephine
Cooper, Gavin
Melville, Jessica Lauren
Harris, Jill
Schall, Ulrich
Loughland, Carmel Maree
Thienel, Renate
Campbell, Linda Elisabet
SpringerLink (Online service)

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Impaired motor inhibition during perceptual inhibition in older, but not younger adults: a psychophysiological study

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Alpha/Beta oscillations indicate inhibition of interfering visual memories

Otologic and audiologic findings in 22q11.2 deletion syndrome

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome

Developmental trajectories of executive functions in 22q11.2 deletion syndrome

Impaired motor inhibition during perceptual inhibition in older, but not younger adults: a psychophysiological study

Mapping the deletion endpoints in individuals with 22q11.2 Deletion Syndrome by droplet digital PCR

An implicit and reliable neural measure quantifying impaired visual coding of facial expression: evidence from the 22q11.2 deletion syndrome

Abnormal development of early auditory processing in 22q11.2 Deletion Syndrome

Intergenerational and intrafamilial phenotypic variability in 22q11.2 Deletion syndrome subjects

Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome

Complement Activation in 22q11.2 Deletion Syndrome

Genotype-phenotype correlation in 22q11.2 deletion syndrome

Alpha/Beta oscillations indicate inhibition of interfering visual memories

Otologic and audiologic findings in 22q11.2 deletion syndrome

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome

Developmental trajectories of executive functions in 22q11.2 deletion syndrome

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Mapping the deletion endpoints in individuals with 22q11.2 Deletion Syndrome by droplet digital PCR

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Intergenerational and intrafamilial phenotypic variability in 22q11.2 Deletion syndrome subjects

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Pre-pulse inhibition and antisaccade performance indicate impaired attention modulation of cognitive inhibition in 22q11.2 deletion syndrome (22q11DS)

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Other Objects (12)

Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome

Complement Activation in 22q11.2 Deletion Syndrome

Genotype-phenotype correlation in 22q11.2 deletion syndrome

Alpha/Beta oscillations indicate inhibition of interfering visual memories

Otologic and audiologic findings in 22q11.2 deletion syndrome

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome

Developmental trajectories of executive functions in 22q11.2 deletion syndrome

Impaired motor inhibition during perceptual inhibition in older, but not younger adults: a psychophysiological study

Mapping the deletion endpoints in individuals with 22q11.2 Deletion Syndrome by droplet digital PCR

An implicit and reliable neural measure quantifying impaired visual coding of facial expression: evidence from the 22q11.2 deletion syndrome

Abnormal development of early auditory processing in 22q11.2 Deletion Syndrome

Intergenerational and intrafamilial phenotypic variability in 22q11.2 Deletion syndrome subjects

Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome

Complement Activation in 22q11.2 Deletion Syndrome

Genotype-phenotype correlation in 22q11.2 deletion syndrome

Alpha/Beta oscillations indicate inhibition of interfering visual memories

Otologic and audiologic findings in 22q11.2 deletion syndrome

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome

Developmental trajectories of executive functions in 22q11.2 deletion syndrome

Impaired motor inhibition during perceptual inhibition in older, but not younger adults: a psychophysiological study

Mapping the deletion endpoints in individuals with 22q11.2 Deletion Syndrome by droplet digital PCR

An implicit and reliable neural measure quantifying impaired visual coding of facial expression: evidence from the 22q11.2 deletion syndrome

Abnormal development of early auditory processing in 22q11.2 Deletion Syndrome

Intergenerational and intrafamilial phenotypic variability in 22q11.2 Deletion syndrome subjects

Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome

Complement Activation in 22q11.2 Deletion Syndrome

Genotype-phenotype correlation in 22q11.2 deletion syndrome

Alpha/Beta oscillations indicate inhibition of interfering visual memories

Otologic and audiologic findings in 22q11.2 deletion syndrome

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome

Developmental trajectories of executive functions in 22q11.2 deletion syndrome

Impaired motor inhibition during perceptual inhibition in older, but not younger adults: a psychophysiological study

Mapping the deletion endpoints in individuals with 22q11.2 Deletion Syndrome by droplet digital PCR

An implicit and reliable neural measure quantifying impaired visual coding of facial expression: evidence from the 22q11.2 deletion syndrome

Abnormal development of early auditory processing in 22q11.2 Deletion Syndrome

Intergenerational and intrafamilial phenotypic variability in 22q11.2 Deletion syndrome subjects

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