Pages that link to "Q36325356"

The following pages link to Hippocampal volume reduction in children with chromosome 22q11.2 deletion syndrome is associated with cognitive impairment (Q36325356):

Displaying 36 items.

• MAP'ing CNS development and cognition: an ERKsome process (Q24621710) (← links)
• Subjective experience of episodic memory and metacognition: a neurodevelopmental approach (Q26853512) (← links)
• Behavioral and Neuroanatomical Phenotypes in Mouse Models of Autism (Q27025227) (← links)
• Dysregulation of presynaptic calcium and synaptic plasticity in a mouse model of 22q11 deletion syndrome (Q28509414) (← links)
• Comprehensive neurocognitive endophenotyping strategies for mouse models of genetic disorders (Q30458768) (← links)
• The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders (Q30468033) (← links)
• Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes (Q30472917) (← links)
• Neuroanatomic predictors to prodromal psychosis in velocardiofacial syndrome (22q11.2 deletion syndrome): a longitudinal study (Q30499844) (← links)
• Postnatal development of the hippocampus in the Rhesus macaque (Macaca mulatta): a longitudinal magnetic resonance imaging study. (Q30581153) (← links)
• Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome (Q33352752) (← links)
• A Synaptic Function Approach to Investigating Complex Psychiatric Diseases (Q33756893) (← links)
• Association of the family environment with behavioural and cognitive outcomes in children with chromosome 22q11.2 deletion syndrome (Q33863797) (← links)
• Decreased DGCR8 expression and miRNA dysregulation in individuals with 22q11.2 deletion syndrome (Q33989539) (← links)
• Increased incidence and size of cavum septum pellucidum in children with chromosome 22q11.2 deletion syndrome (Q33999011) (← links)
• Regional cortical volumes and congenital heart disease: a MRI study in 22q11.2 deletion syndrome (Q34284040) (← links)
• How might stress contribute to increased risk for schizophrenia in children with chromosome 22q11.2 deletion syndrome? (Q34669660) (← links)
• Disrupted fornix integrity in children with chromosome 22q11.2 deletion syndrome (Q35499123) (← links)
• Hippocampal malrotation is associated with chromosome 22q11.2 microdeletion. (Q35695653) (← links)
• The hippocampi of children with chromosome 22q11.2 deletion syndrome have localized anterior alterations that predict severity of anxiety (Q36858439) (← links)
• Schizopsychotic symptom-profiles and biomarkers: beacons in diagnostic labyrinths (Q37346444) (← links)
• Neuroanatomical phenotypes in a mouse model of the 22q11.2 microdeletion (Q37412947) (← links)
• Evidence of gray matter reduction and dysfunction in chromosome 22q11.2 deletion syndrome. (Q37480286) (← links)
• System-based proteomic and metabonomic analysis of the Df(16)A+/- mouse identifies potential miR-185 targets and molecular pathway alterations (Q37660911) (← links)
• Autism spectrum disorder: neuropathology and animal models (Q39353531) (← links)
• Partial least squares correlation of multivariate cognitive abilities and local brain structure in children and adolescents (Q43571963) (← links)
• Baseline connectome modular abnormalities in the childhood phase of a longitudinal study on individuals with chromosome 22q11.2 deletion syndrome. (Q46408355) (← links)
• Visual processing of emotional dynamic faces in 22q11.2 deletion syndrome (Q47597196) (← links)
• Time-based prospective memory in children and adolescents with 22q11.2 deletion syndrome (Q47842772) (← links)
• Vitamin D deficiency, behavioral atypicality, anxiety and depression in children with chromosome 22q11.2 deletion syndrome. (Q48036597) (← links)
• Neuropsychological profile of Italian children and adolescents with 22q11.2 deletion syndrome with and without intellectual disability (Q50789313) (← links)
• Nonverbal and verbal learning: A comparative study of children and adolescents with 22q11 deletion syndrome, non-syndromal Nonverbal Learning Disorder and memory disorder (Q51007907) (← links)
• Neuroradiographic findings in 22q11.2 deletion syndrome. (Q52092679) (← links)
• Nr2f1 heterozygous knockout mice recapitulate neurological phenotypes of Bosch-Boonstra-Schaaf optic atrophy syndrome and show impaired hippocampal synaptic plasticity (Q90631922) (← links)
• Intrauterine growth restriction and development of the hippocampus: implications for learning and memory in children and adolescents (Q91589117) (← links)
• Magnitude and heterogeneity of brain structural abnormalities in 22q11.2 deletion syndrome: a meta-analysis (Q92564640) (← links)
• Positive psychotic symptoms are associated with divergent developmental trajectories of hippocampal volume during late adolescence in patients with 22q11DS (Q95499528) (← links)