A new account of the neurocognitive foundations of impairments in space, time and number processing in children with chromosome 22q11.2 deletion syndrome.
about
Mathematical learning disabilities in special populations: phenotypic variation and cross-disorder comparisons.Comprehensive neurocognitive endophenotyping strategies for mouse models of genetic disordersChildren with chromosome 22q11.2 deletion syndrome exhibit impaired spatial working memory.Applicability of the nonverbal learning disability paradigm for children with 22q11.2 deletion syndrome.The development of cognitive control in children with chromosome 22q11.2 deletion syndromeAssociation of the family environment with behavioural and cognitive outcomes in children with chromosome 22q11.2 deletion syndrome.Temporal ordering deficits in female CGG KI mice heterozygous for the fragile X premutation.Increased incidence and size of cavum septum pellucidum in children with chromosome 22q11.2 deletion syndrome.The cognitive phenotype of spina bifida meningomyeloceleAtypical functional brain activation during a multiple object tracking task in girls with Turner syndrome: neurocorrelates of reduced spatiotemporal resolutionYoung adult female fragile X premutation carriers show age- and genetically-modulated cognitive impairments.Atypical development of the executive attention network in children with chromosome 22q11.2 deletion syndromeMagnitude representations in Williams syndrome: differential acuity in time, space and number processingSocial impairments in chromosome 22q11.2 deletion syndrome (22q11.2DS): autism spectrum disorder or a different endophenotype?Clues to the foundations of numerical cognitive impairments: evidence from genetic disorders.Female CGG knock-in mice modeling the fragile X premutation are impaired on a skilled forelimb reaching taskThe importance of considering all attributes of memory in behavioral endophenotyping of mouse models of genetic disease.A cross-sectional study of the development of volitional control of spatial attention in children with chromosome 22q11.2 deletion syndromeImpaired multiple object tracking in children with chromosome 22q11.2 deletion syndromeSpatiotemporal processing deficits in female CGG KI mice modeling the fragile X premutation.CGG trinucleotide repeat length modulates neural plasticity and spatiotemporal processing in a mouse model of the fragile X premutation.Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms.Shared deficits in space, time, and quantity processing in childhood genetic disordersVisual perception and processing in children with 22q11.2 deletion syndrome: associations with social cognition measures of face identity and emotion recognitionMagnitude Processing in the Brain: An fMRI Study of Time, Space, and Numerosity as a Shared Cortical SystemNeurocognitive endophenotypes in CGG KI and Fmr1 KO mouse models of Fragile X-Associated disorders: an analysis of the state of the fieldCommon and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes.Facial emotion perception by intensity in children and adolescents with 22q11.2 deletion syndrome.Progressive spatial processing deficits in a mouse model of the fragile X premutation.The 1000 Genomes Project: deep genomic sequencing waiting for deep psychiatric phenotyping.Baseline connectome modular abnormalities in the childhood phase of a longitudinal study on individuals with chromosome 22q11.2 deletion syndrome.Social cognition dysfunction in adolescents with 22q11.2 deletion syndrome (velo-cardio-facial syndrome): relationship with executive functioning and social competence/functioning.Adaptation of the Arizona Cognitive Task Battery for use with the Ts65Dn mouse model (Mus musculus) of Down syndrome.Visual processing deficits in 22q11.2 Deletion Syndrome.Neuropsychological profile of Italian children and adolescents with 22q11.2 deletion syndrome with and without intellectual disability.
P2860
Q30433108-192DFFAD-4222-43A7-9851-6EDD37DD17DBQ30458768-D9F91E06-D2EA-40EA-8683-3B83F16A8BEFQ33675258-0688B85F-526A-40BD-9AF9-4AAE0B7CEDCBQ33710925-F521C976-EAAA-4624-89E2-9D417257B321Q33730345-0734BF44-69F5-412E-81D3-6E68A745F8B2Q33863797-1A907858-2F4F-443B-8BE8-C0FE6E30F300Q33987114-174112DB-C27A-43D6-8C25-9486A65AE84BQ33999011-F0D624ED-AA2E-495B-9C1D-1AE292842C98Q34074873-07432516-52A3-4C28-9064-31A0CE2DCEEEQ34257136-280F3600-064A-4EF0-8A7B-6532D6F23DA4Q34630352-9423DD71-D4B6-44FF-893F-05906E073742Q34669665-EEF68503-E35F-44D3-80DE-FD208E6EAA61Q34981039-A56DDB67-1AEF-45A6-AF3F-6629F1D19464Q35083203-B2C4C9AC-6A33-46E3-BC7C-72CA963D4680Q35153422-D3771E2A-4D5E-4381-A438-DFAF93A48C0AQ35754126-BD250D19-2A6F-48F5-81B5-95AC4B8D0D5BQ36008766-F1201A07-A6A4-4EA3-A619-9AA367A97BB5Q36028885-F49316E2-7B98-4AB9-B9A6-036A0FE2D6AEQ36028889-357E7AE7-1CA9-4FF3-A663-6051FA30B242Q36044469-D5E972CD-9AEB-4650-B157-9B9214C5F66AQ36253268-DE6746A9-383A-4863-89C9-D02EFAC4E071Q36253405-C742A2F2-355F-4D68-AA51-639AF2CBD2F1Q36593257-1F506517-1D60-4849-8F77-3BC9C5FAEBCBQ37182360-F3371684-EFB5-490A-A921-D366839D2C2EQ37310015-D8F4CE76-00D8-413A-A485-089173D60846Q37623407-5D5AF11E-A3FF-424B-9BC4-1826822353BDQ37716526-E417106B-7001-4D07-BB0C-1F0AE825C39DQ38987751-5205325B-BFB4-4413-857E-F42CF377DD23Q42119514-86E03EE1-B556-42F1-B63F-600373B105E0Q42720402-A7FC3C56-9F07-4E3B-B48E-5B00925FD060Q46408355-73E14895-369A-4922-AE1E-FCEFFBE45CBEQ47738547-74364945-C967-47A6-9609-2B9C6A20511DQ48370031-C9F8B054-855D-44F1-BA7D-AF92A3820D6CQ50419917-0CC2DE84-6342-4D01-B566-670A11E4ACF7Q50789313-89FF8418-9CFE-4D32-B484-11627D3E7B3A
P2860
A new account of the neurocognitive foundations of impairments in space, time and number processing in children with chromosome 22q11.2 deletion syndrome.
description
2008 nî lūn-bûn
@nan
2008 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
A new account of the neurocogn ...... ome 22q11.2 deletion syndrome.
@ast
A new account of the neurocogn ...... ome 22q11.2 deletion syndrome.
@en
type
label
A new account of the neurocogn ...... ome 22q11.2 deletion syndrome.
@ast
A new account of the neurocogn ...... ome 22q11.2 deletion syndrome.
@en
prefLabel
A new account of the neurocogn ...... ome 22q11.2 deletion syndrome.
@ast
A new account of the neurocogn ...... ome 22q11.2 deletion syndrome.
@en
P2860
P356
P1476
A new account of the neurocogn ...... ome 22q11.2 deletion syndrome.
@en
P2093
Tony J Simon
P2860
P356
10.1002/DDRR.8
P577
2008-01-01T00:00:00Z