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        325-336 of 970 results for 'Autism'

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        A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric Cohorts

        The SNP-based heritability for ADHD symptom scores indicates a polygenic architecture, and genes involved in neurite outgrowth are possibly involved ...

        Research

        Vitamin D in fetal development: Findings from a birth cohort study

        Birth cohort studies provide an invaluable resource for studies of the influence of the fetal environment on health in later life. ...

        Research

        Late-talking and risk for behavioural and emotional problems during childhood and adolescence

        Although many toddlers with expressive vocabulary delay ("late talkers") present with age-appropriate language skills by the time they are of school age... ...

        Research

        Comparative analysis of outcome measures used in examining neurodevelopmental effects of early childhood anesthesia exposure

        This paper reports on data from the Western Australian Pregnancy Cohort (Raine) Study to examine whether exposure to anesthetics in children younger than 3... ...

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        Fetal Testosterone, Socio-Emotional Engagement and Language Development

        The present study investigated the relations among fetal testosterone, child socio-emotional engagement and language development... ...

        Research

        Sex-specific associations between umbilical cord blood testosterone levels and language delay in early childhood

        Preliminary evidence suggests that prenatal testosterone exposure may be associated with language delay. However, no study has examined a large sample of... ...

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        Epidemiology of Hospital Admissions for Craniosynostosis in Australia: A Population-Based Study

        To describe trends, age, and sex-specific patterns of population hospital admissions with a diagnosis of craniosynostosis (CS) in Australia. Population data for hospital separations (in-patient) from public and private hospitals (July 1996-June 2018) were obtained from the publicly available Australian Institute of Health and Welfare (AIHW) National Hospital Morbidity Database. ...

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        Health conditions and their impact among adolescents and young adults with down syndrome

        The aim of this study was to examine the prevalence of medical conditions and use of health services among young adults with Down syndrome and describe the... ...

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        Admissions in Children with Down Syndrome: Experience of a Population-Based Cohort Followed from Birth

        This study describes patterns of hospitalisations for children and young people with Down syndrome in Western Australia. ...

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        The experiences of mothers of young adults with an intellectual disability transitioning from secondary school to adult life

        The transition from school to adulthood for young adults with an intellectual disability involves movement from a generally secure and supported school... ...

        Research

        What does the nature of the MECP2 mutation tell us about parental origin and recurrence risk in Rett syndrome?

        The MECP2 mutations occurring in the severe neurological disorder Rett syndrome are predominantly de novo, with rare familial cases. The aims of this study... ...

        Research

        Delineation of large deletions of the MECP2 gene in Rett syndrome patients, including a familial case with a male proband

        Comprehensive genetic screening programs have led to the identification of pathogenic methyl-CpG-binding protein 2 (MECP2) mutations... ...

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