CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problemsUse of model systems to understand the etiology of fragile X-associated primary ovarian insufficiency (FXPOI)Journal of Neurodevelopmental Disorders is now a fully open access journalWhole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.Rapid automatized naming as an index of genetic liability to autismCommon circuit defect of excitatory-inhibitory balance in mouse models of autism.Complexities of X chromosome inactivation status in female human induced pluripotent stem cells-a brief review and scientific update for autism researchThe multiple molecular facets of fragile X-associated tremor/ataxia syndromeA quantitative measure of restricted and repetitive behaviors for early childhood.Methods for acquiring MRI data in children with autism spectrum disorder and intellectual impairment without the use of sedationA functional neuroimaging study of fusiform response to restricted interests in children and adolescents with autism spectrum disorder.Investigating the effects of copy number variants on reading and language performance.Specific pattern of maturation and differentiation in the formation of cortical tubers in tuberous sclerosis omplex (TSC): evidence from layer-specific marker expressionReduced engagement with social stimuli in 6-month-old infants with later autism spectrum disorder: a longitudinal prospective study of infants at high familial riskNeural selectivity for communicative auditory signals in Phelan-McDermid syndrome.Genomic sequencing of a dyslexia susceptibility haplotype encompassing ROBO1.Complete or partial reduction of the Met receptor tyrosine kinase in distinct circuits differentially impacts mouse behaviorWnt signaling networks in autism spectrum disorder and intellectual disabilityA new synaptic player leading to autism risk: Met receptor tyrosine kinasePhelan-McDermid syndrome: a review of the literature and practice parameters for medical assessment and monitoringInfant siblings and the investigation of autism risk factorsFunctional characterization of rare FOXP2 variants in neurodevelopmental disorder.Violence: heightened brain attentional network response is selectively muted in Down syndromeOf mice and monkeys: using non-human primate models to bridge mouse- and human-based investigations of autism spectrum disordersLanguage development after cochlear implantation: an epigenetic modelA family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3The NIH Toolbox Cognitive Battery for intellectual disabilities: three preliminary studies and future directionsAtypical sound discrimination in children with ASD as indicated by cortical ERPs.Automatic cortical representation of auditory pitch changes in Rett syndrome.Neurophysiological hyperresponsivity to sensory input in autism spectrum disorders.Characterization of Rett Syndrome-like phenotypes in Mecp2-knockout ratsLimited impact of Cntn4 mutation on autism-related traits in developing and adult C57BL/6J mice.Speech motor planning and execution deficits in early childhood stuttering.Pre-pulse inhibition and antisaccade performance indicate impaired attention modulation of cognitive inhibition in 22q11.2 deletion syndrome (22q11DS).Late, not early mismatch responses to changes in frequency are reduced or deviant in children with dyslexia: an event-related potential study.Abnormal late visual responses and alpha oscillations in neurofibromatosis type 1: a link to visual and attention deficits.Reward processing in autism: a thematic series.Genetics and language: a neurobiological perspective on the missing link (-ing hypotheses).Using animal models of enriched environments to inform research on sensory integration intervention for the rehabilitation of neurodevelopmental disordersVerbal short-term memory deficits in Down syndrome: phonological, semantic, or both?
P1433
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P1433
description
journal
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revista científica
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rivista scientifica
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vědecký časopis
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wetenschappelijk tijdschrift van BioMed Central
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wissenschaftliche Fachzeitschrift
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مجلة
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वैज्ञानिक पत्रिका
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name
Journal of Neurodevelopmental Disorders
@ast
Journal of Neurodevelopmental Disorders
@en
Journal of Neurodevelopmental Disorders
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Journal of Neurodevelopmental Disorders
@it
Journal of Neurodevelopmental Disorders
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type
label
Journal of Neurodevelopmental Disorders
@ast
Journal of Neurodevelopmental Disorders
@en
Journal of Neurodevelopmental Disorders
@es
Journal of Neurodevelopmental Disorders
@it
Journal of Neurodevelopmental Disorders
@nl
prefLabel
Journal of Neurodevelopmental Disorders
@ast
Journal of Neurodevelopmental Disorders
@en
Journal of Neurodevelopmental Disorders
@es
Journal of Neurodevelopmental Disorders
@it
Journal of Neurodevelopmental Disorders
@nl
P31
P243
P3181
P1055
P1058
P1156
19400158590
P1160
J. Neurodev. Disord.
P123
P1277
P1476
Journal of Neurodevelopmental Disorders
@en
P166
P236
P243
P3181
P407
P5115
P571
2009-01-01T00:00:00Z