Visual memory profile in 22q11.2 microdeletion syndrome: are there differences in performance and neurobiological substrates between tasks linked to ventral and dorsal visual brain structures? A cross-sectional and longitudinal study (Q37408865)

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English	Visual memory profile in 22q11.2 microdeletion syndrome: are there differences in performance and neurobiological substrates between tasks linked to ventral and dorsal visual brain structures? A cross-sectional and longitudinal study	scientific article

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scholarly article

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Europe PubMed Central

PMC publication ID

20 August 2017

Visual memory profile in 22q11.2 microdeletion syndrome: are there differences in performance and neurobiological substrates between tasks linked to ventral and dorsal visual brain structures? A cross-sectional and longitudinal study (English)

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

microdeletion syndrome

1 reference

based on heuristic

inferred from title

10

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Stephan Eliez

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Europe PubMed Central

PMC publication ID

20 August 2017

Mathilde Bostelmann

object named as

Mathilde Bostelmann

1

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Martin Debbané

object named as

Martin Debbané

7

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5

object named as

Marie Schaer

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Maude Schneider

2

object named as

Maude Schneider

1 reference

Europe PubMed Central

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20 August 2017

6

object named as

Elisa Scariati

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

author name string

Maria Carmela Padula

3

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Johanna Maeder

4

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Bronwyn Glaser

8

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Sarah Menghetti

9

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Europe PubMed Central

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20 August 2017

language of work or name

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based on heuristic

inferred from title

publication date

10 November 2016

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Europe PubMed Central

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20 August 2017

Journal of Neurodevelopmental Disorders

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Europe PubMed Central

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20 August 2017

8

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

41

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

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

1 reference

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Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies

1 reference

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6 September 2017

Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome

1 reference

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6 September 2017

The development of cognitive control in children with chromosome 22q11.2 deletion syndrome

1 reference

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6 September 2017

Children with chromosome 22q11.2 deletion syndrome exhibit impaired spatial working memory

1 reference

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Measuring forgetting: a critical review of accelerated long-term forgetting studies

1 reference

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6 September 2017

Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome

1 reference

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Neurocognitive development in 22q11.2 deletion syndrome: comparison with youth having developmental delay and medical comorbidities

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Subjective experience of episodic memory and metacognition: a neurodevelopmental approach

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Psychopathology and cognition in children with 22q11.2 deletion syndrome

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6 September 2017

Genetic contributions to changes of fiber tracts of ventral visual stream in 22q11.2 deletion syndrome

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6 September 2017

The ventral visual pathway: an expanded neural framework for the processing of object quality

1 reference

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6 September 2017

Reduced fractional anisotropy and axial diffusivity in white matter in 22q11.2 deletion syndrome: a pilot study

1 reference

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6 September 2017

Atlas-based white matter analysis in individuals with velo-cardio-facial syndrome (22q11.2 deletion syndrome) and unaffected siblings

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5105283

6 September 2017

Computerized neurocognitive profile in young people with 22q11.2 deletion syndrome compared to youths with schizophrenia and at-risk for psychosis

1 reference

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6 September 2017

From genes to brain development to phenotypic behavior: "dorsal-stream vulnerability" in relation to spatial cognition, attention, and planning of actions in Williams syndrome (WS) and other developmental disorders

1 reference

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6 September 2017

Neurodevelopment of the visual system in typically developing children.

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6 September 2017

A new neural framework for visuospatial processing

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6 September 2017

Event-related fMRI studies of episodic encoding and retrieval: meta-analyses using activation likelihood estimation

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6 September 2017

Associations between performance on the Rey-Osterrieth Complex Figure and regional brain volumes in children with and without velocardiofacial syndrome

1 reference

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6 September 2017

Velo-cardio-facial syndrome: 30 Years of study

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6 September 2017

Atypical cortical connectivity and visuospatial cognitive impairments are related in children with chromosome 22q11.2 deletion syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5105283

6 September 2017

Verbal short-term memory in individuals with chromosome 22q11.2 deletion: specific deficit in serial order retention capacities?

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6 September 2017

Smoothing and cluster thresholding for cortical surface-based group analysis of fMRI data

1 reference

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6 September 2017

The cognitive neuroscience of remote episodic, semantic and spatial memory

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6 September 2017

An automated labeling system for subdividing the human cerebral cortex on MRI scans into gyral based regions of interest

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6 September 2017

Functional neuroanatomy of remote episodic, semantic and spatial memory: a unified account based on multiple trace theory

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Conscious intention and motor cognition

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6 September 2017

Neuropsychological characteristics of children with the 22q11 Deletion Syndrome: a descriptive analysis

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6 September 2017

Clinical use of the Benton Visual Retention Test for children and adolescents with learning disabilities

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6 September 2017

Normal and anomalous development of visual motion processing: motion coherence and 'dorsal-stream vulnerability'.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5105283

6 September 2017

Chromosome 22q11 deletion syndrome: update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications

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6 September 2017

Measuring the thickness of the human cerebral cortex from magnetic resonance images

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6 September 2017

Neuropsychological, learning and psychosocial profile of primary school aged children with the velo-cardio-facial syndrome (22q11 deletion): evidence for a nonverbal learning disability?

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5105283

6 September 2017

Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome

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6 September 2017

Cortical surface-based analysis. II: Inflation, flattening, and a surface-based coordinate system

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The hippocampal formation participates in novel picture encoding: evidence from functional magnetic resonance imaging.

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Distinct neural correlates of visual long-term memory for spatial location and object identity: a positron emission tomography study in humans

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6 September 2017

Information Processing in the Primate Visual System: An Integrated Systems Perspective

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6 September 2017

Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome

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6 September 2017

A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome

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6 September 2017

The motor profile of primary school-age children with a 22q11.2 deletion syndrome (22q11.2DS) and an age- and IQ-matched control group

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'What' and 'where' in the human brain

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Presenting phenotype in 100 children with the 22q11 deletion syndrome.

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Parietal cortex: from sight to action

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26 June 2018

A specific deficit of dorsal stream function in Williamsʼ syndrome

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Congenital absence of the thymus

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Risk factors and the evolution of psychosis in 22q11.2 deletion syndrome: a longitudinal 2-site study

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2 September 2018

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Sex differences in thickness, and folding developments throughout the cortex

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Cognitive development in children with 22q11.2 deletion syndrome

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2 September 2018

Preliminary structure and predictive value of attenuated negative symptoms in 22q11.2 deletion syndrome

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2 September 2018

Neuropsychological profile of Italian children and adolescents with 22q11.2 deletion syndrome with and without intellectual disability

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2 September 2018

Visual scanpath abnormalities in 22q11.2 deletion syndrome: is this a face specific deficit?

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2 September 2018

Nonverbal and verbal learning: A comparative study of children and adolescents with 22q11 deletion syndrome, non-syndromal Nonverbal Learning Disorder and memory disorder

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2 September 2018

Eye gaze during face processing in children and adolescents with 22q11.2 deletion syndrome

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2 September 2018

Differentiating maturational and aging-related changes of the cerebral cortex by use of thickness and signal intensity

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2 September 2018

Executive functions and memory abilities in children with 22q11.2 deletion syndrome

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5105283

2 September 2018

A comparative study of cognition and brain anatomy between two neurodevelopmental disorders: 22q11.2 deletion syndrome and Williams syndrome

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5105283

2 September 2018

Encoding and retrieval processes in velo-cardio-facial syndrome (VCFS).

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2 September 2018

Impaired activation of face processing networks revealed by functional magnetic resonance imaging in 22q11.2 deletion syndrome

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5105283

2 September 2018

COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5105283

2 September 2018

Visual and spatial long-term memory: differential pattern of impairments in Williams and Down syndromes.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5105283

2 September 2018

Memory and learning in children with 22q11.2 deletion syndrome: evidence for ventral and dorsal stream disruption?

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2 September 2018

Integrative cortical dysfunction and pervasive motion perception deficit in fragile X syndrome.

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2 September 2018

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2 September 2018

Psychometric construction of the Rey-Osterrieth Complex Figure: methodological considerations and interrater reliability.

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2 September 2018

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2 September 2018

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2 September 2018

The neurocognitive phenotype of the 22q11.2 deletion syndrome: selective deficit in visual-spatial memory.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5105283

2 September 2018

An investigation of the neuropsychological profile in adults with velo-cardio-facial syndrome (VCFS).

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2 September 2018

All developmental dyslexic subtypes display an elevated motion coherence threshold

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2 September 2018

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2 September 2018

Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion

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2 September 2018

Motion processing in autism: evidence for a dorsal stream deficiency

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2 September 2018

Object and spatial visual working memory activate separate neural systems in human cortex.

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2 September 2018

Intellectual abilities in a large sample of children with Velo-Cardio-Facial Syndrome: an update

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based on heuristic

inferred from PubMed ID database lookup

Structural changes to the fusiform gyrus: A cerebral marker for social impairments in 22q11.2 deletion syndrome?

1 reference

https://pubmed.ncbi.nlm.nih.gov/27843501

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/S11689-016-9174-5

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

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