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        109-120 of 720 results for 'Neurodevelopmental'

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        Common Pathways to NSSI and Suicide Ideation: The Roles of Rumination and Self-Compassion

        The salience of self-compassion offers promise for early intervention initiatives focusing on less judgmental or self-critical means of self-relation ...

        Research

        Fish Oil

        Claims have been made about the benefits of fish oil supplementation. However, our research, including studies in collaboration with colleagues from Adelaide University, has suggested harm. Jasani B, et al. Longchain polyunsaturated fatty acid ...

        Research

        Implementation of the National Guideline for the Assessment and Diagnosis of ASD in Australia – Health Sector Capacity Building

        Andrew Whitehouse Watch and listen to Andrew AJ PhD Angela Wright Bennett Professor of Autism Research at Telethon Kids Institute; Director, CliniKids Andrew.Whitehouse@telethonkids.org.au Angela Wright Bennett Professor of Autism Research at ...

        Research

        Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank

        Autism spectrum disorder (ASD) is a complex neurodevelopmental condition whose biological basis is yet to be elucidated. The Australian Autism Biobank (AAB) is an initiative of the Cooperative Research Centre for Living with Autism (Autism CRC) to establish an Australian resource of biospecimens, phenotypes and genomic data for research on autism. ...

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        Survival with Rett syndrome: comparing Rett's original sample with data from the Australian Rett syndrome Database

        Rett syndrome is a severe neurodevelopmental disorder that typically affects females. Little is known about the natural history and survival time of these femal ...

        Research

        Co-designing a trauma-informed program for parents whose infant has had a Neonatal Intensive Care Unit (NICU) admission

        Alix Helen Lisa Nicole Woolard Milroy McGivern Wickens AW HM LM NW BPsych (Hons), PhD MBBS; FRANZCP; CATCAP BA (Hons 1, Psych) BHlthSc (Hons) Senior Research Fellow Honorary Research Fellow Research Assistant Program Coordinator 08 6319 1823 08 6319 ...

        Research

        Treatment for Childhood and Adolescent Dissociation: A Systematic Review

        Dissociative symptoms are linked to experiences of trauma, often originating in childhood and adolescence. Dissociative disorders are associated with a high burden of illness and a poor quality of life. Despite evidence suggesting that early intervention can improve outcomes, little research exists on the treatment of dissociative disorders in childhood and adolescence. ...

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        Development of an International Database for a Rare Genetic Disorder: The MECP2 Duplication Database (MDBase)

        The natural history of MECP2 duplication syndrome (MDS), a rare X-linked neurodevelopmental disorder with an estimated birth prevalence of 1/150,000 live births, is poorly understood due to a lack of clinical data collected for research. Such information is critical to the understanding of disease progression, therapeutic endpoints and outcome measures for clinical trials, as well as the development of therapies and orphan products. ...

        Research

        The Demographic and Neurocognitive Profile of Clients Diagnosed With Fetal Alcohol Spectrum Disorder in PATCHES Paediatrics Clinics

        The aim of this study was to describe the demographic and neurocognitive profile of the first 199 individuals diagnosed with FASD in PATCHES Paediatrics clinics ...

        Research

        Associations between the human immune system and gut microbiome with neurodevelopment in the first 5 years of life: A systematic scoping review

        The aim of this review was to map the literature assessing associations between maternal or infant immune or gut microbiome biomarkers and child neurodevelopmental outcomes within the first 5 years of life. We conducted a PRISMA-ScR compliant review of peer-reviewed, English-language journal articles. ...

        Research

        A brief history of MECP2 duplication syndrome: 20-years of clinical understanding

        MECP2 duplication syndrome (MDS) is a rare, X-linked, neurodevelopmental disorder caused by a duplication of the methyl-CpG-binding protein 2 (MECP2) gene-a gene in which loss-of-function mutations lead to Rett syndrome (RTT). MDS has an estimated live birth prevalence in males of 1/150,000. ...

        Research

        Fetal alcohol spectrum disorder and youth justice: a prevalence study among young people sentenced to detention in Western Australia

        This study of young people in detention in Western Australia, has documented a high prevalence of FASD and severe neurodevelopmental impairment ...

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