Neuroanatomic predictors to prodromal psychosis in velocardiofacial syndrome (22q11.2 deletion syndrome): a longitudinal study
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Converging levels of analysis on a genomic hotspot for psychosis: insights from 22q11.2 deletion syndromeDendritic spine pathology in schizophreniaThe Danish 22q11 research initiativeA comparison of FreeSurfer-generated data with and without manual intervention.The development of cognitive control in children with chromosome 22q11.2 deletion syndrome22q11 deletion syndrome: a review of the neuropsychiatric features and their neurobiological basis.Altered white matter microstructure is associated with social cognition and psychotic symptoms in 22q11.2 microdeletion syndrome.White matter microstructural abnormalities of the cingulum bundle in youths with 22q11.2 deletion syndrome: associations with medication, neuropsychological function, and prodromal symptoms of psychosisAssociation between autism spectrum disorder in individuals with velocardiofacial (22q11.2 deletion) syndrome and PRODH and COMT genotypesCognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndromeDisrupted fornix integrity in children with chromosome 22q11.2 deletion syndromeCortical gyrification in velo-cardio-facial (22q11.2 deletion) syndrome: a longitudinal studyIncreased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms.Reduced fractional anisotropy and axial diffusivity in white matter in 22q11.2 deletion syndrome: a pilot study.Clinical and genetic high-risk paradigms: converging paths to psychosis meet in the temporal lobes.The stress-induced cytokine interleukin-6 decreases the inhibition/excitation ratio in the rat temporal cortex via trans-signaling.The hippocampi of children with chromosome 22q11.2 deletion syndrome have localized anterior alterations that predict severity of anxiety.Social cognition in 22q11.2 microdeletion syndrome: relevance to psychosis?A cross-sectional analysis of the development of response inhibition in children with chromosome 22q11.2 deletion syndromeA longitudinal examination of the psychoeducational, neurocognitive, and psychiatric functioning in children with 22q11.2 deletion syndromeThe 22q11.2 deletion syndrome as a window into complex neuropsychiatric disorders over the lifespan.White matter abnormalities in 22q11.2 deletion syndrome: preliminary associations with the Nogo-66 receptor gene and symptoms of psychosisShyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome.Secondary psychoses: an update.Long-range dysconnectivity in frontal and midline structures is associated to psychosis in 22q11.2 deletion syndrome.Structural abnormalities in cortical volume, thickness, and surface area in 22q11.2 microdeletion syndrome: Relationship with psychotic symptoms.Altered cognitive development in the siblings of individuals with schizophrenia.Intrinsic Connectivity Network-Based Classification and Detection of Psychotic Symptoms in Youth With 22q11.2 Deletions.Axis I psychiatric diagnoses in adolescents and young adults with 22q11 deletion syndrome.Longitudinal study of cerebral surface morphology in youth with 22q11.2 deletion syndrome, and association with positive symptoms of psychosis.Baseline connectome modular abnormalities in the childhood phase of a longitudinal study on individuals with chromosome 22q11.2 deletion syndrome.Longitudinal study of premorbid adjustment in 22q11.2 deletion (velocardiofacial) syndrome and association with psychosis.Associations between neurodevelopmental genes, neuroanatomy, and ultra high risk symptoms of psychosis in 22q11.2 deletion syndrome.Depression and anxiety disorders in children and adolescents with velo-cardio-facial syndrome (VCFS).Distinct white-matter aberrations in 22q11.2 deletion syndrome and patients at ultra-high risk for psychosis.Cortical Development Requires Mesodermal Expression of Tbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome.Cortical morphology development in patients with 22q11.2 deletion syndrome at ultra-high risk of psychosis.Visual processing deficits in 22q11.2 Deletion Syndrome.Craniofacial dysmorphology in 22q11.2 deletion syndrome by 3D laser surface imaging and geometric morphometrics: illuminating the developmental relationship to risk for psychosis.Caracterização do perfil comportamental e de competência social de indivíduos com a síndrome del22q11.2
P2860
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P2860
Neuroanatomic predictors to prodromal psychosis in velocardiofacial syndrome (22q11.2 deletion syndrome): a longitudinal study
description
2010 nî lūn-bûn
@nan
2010 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Neuroanatomic predictors to pr ...... yndrome): a longitudinal study
@ast
Neuroanatomic predictors to pr ...... yndrome): a longitudinal study
@en
type
label
Neuroanatomic predictors to pr ...... yndrome): a longitudinal study
@ast
Neuroanatomic predictors to pr ...... yndrome): a longitudinal study
@en
prefLabel
Neuroanatomic predictors to pr ...... yndrome): a longitudinal study
@ast
Neuroanatomic predictors to pr ...... yndrome): a longitudinal study
@en
P2093
P2860
P1476
Neuroanatomic predictors to pr ...... yndrome): a longitudinal study
@en
P2093
Anne Marie Higgins
Christopher McCarthy
Jo-Anna Botti
Kevin M Antshel
Lauren Kelchner
Robert J Shprintzen
Wanda P Fremont
Wendy R Kates
P2860
P304
P356
10.1016/J.BIOPSYCH.2010.10.027
P407
P577
2010-12-31T00:00:00Z