(Q37626841)

English

White matter microstructural abnormalities in girls with chromosome 22q11.2 deletion syndrome, Fragile X or Turner syndrome as evidenced by diffusion tensor imaging

scientific article published on 18 April 2013

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

White matter microstructural abnormalities in girls with chromosome 22q11.2 deletion syndrome, Fragile X or Turner syndrome as evidenced by diffusion tensor imaging (English)

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

1 reference

based on heuristic

inferred from title

Turner syndrome

1 reference

based on heuristic

inferred from title

4

object named as

Arthur W Toga

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Paul M. Thompson

5

object named as

Paul M Thompson

0 references

3

object named as

Elliott Beaton

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

2

object named as

Neda Jahanshad

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Julio E. Villalon-Reina

1

object named as

Julio Villalon-Reina

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

author name string

Tony J Simon

6

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

language of work or name

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publication date

18 April 2013

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

81

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

441-454

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Clues to the foundations of numerical cognitive impairments: evidence from genetic disorders

1 reference

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23 August 2017

Diffusion tensor imaging and beyond

1 reference

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Association of schizophrenia in 22q11.2 deletion syndrome and gray matter volumetric deficits in the superior temporal gyrus

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Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome

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

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Neuropathologic features in adults with 22q11.2 deletion syndrome.

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Microstructural maturation of the human brain from childhood to adulthood

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Selective alterations of white matter associated with visuospatial and sensorimotor dysfunction in turner syndrome

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Visuospatial executive function in Turner syndrome: functional MRI and neurocognitive findings

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Research on behavioral phenotypes: velocardiofacial syndrome (deletion 22q11.2).

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[Neuropathology of the Turner syndrome]

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947617

1 September 2018

Functional brain imaging study of mathematical reasoning abilities in velocardiofacial syndrome (del22q11.2)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947617

1 September 2018

Structural brain abnormalities associated with deletion at chromosome 22q11: quantitative neuroimaging study of adults with velo-cardio-facial syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947617

1 September 2018

Regional cortical white matter reductions in velocardiofacial syndrome: a volumetric MRI analysis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947617

1 September 2018

Children and adolescents with velocardiofacial syndrome: a volumetric MRI study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947617

1 September 2018

Spatial cognition in males with Fragile-X syndrome: evidence for a neuropsychological phenotype.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947617

1 September 2018

The effects of X monosomy on brain development: monozygotic twins discordant for Turner's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947617

1 September 2018

Neurodevelopmental effects of the FMR-1 full mutation in humans.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3947617

1 September 2018

Abnormal patterns of cortical gyrification in velo-cardio-facial syndrome (deletion 22q11.2): an MRI study

1 reference

https://pubmed.ncbi.nlm.nih.gov/23602925

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Brain anatomy in Turner syndrome: evidence for impaired social and spatial-numerical networks

1 reference

https://pubmed.ncbi.nlm.nih.gov/23602925

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/23602925

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cortical dysgenesis in a patient with Turner mosaicism

1 reference

https://pubmed.ncbi.nlm.nih.gov/23602925

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-chromosome effects on female brain: a magnetic resonance imaging study of Turner's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/23602925

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diffusion tensor imaging of normal white matter maturation from late childhood to young adulthood: voxel-wise evaluation of mean diffusivity, fractional anisotropy, radial and axial diffusivities, and correlation with reading development

1 reference

https://pubmed.ncbi.nlm.nih.gov/23602925

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Turner syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/23602925

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurodevelopmental effects of X monosomy: a volumetric imaging study

1 reference

https://pubmed.ncbi.nlm.nih.gov/23602925

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.NEUROIMAGE.2013.04.028

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

DBLP publication ID

journals/neuroimage/Villalon-ReinaJBTTS13

1 reference

DBLP Dataset 2021-01-02

28 January 2021

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

ResearchGate publication ID

0 references

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