Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Alexandra, Ure"'
Publikováno v:
Systematic Reviews, Vol 10, Iss 1, Pp 1-6 (2021)
Abstract Background Autism spectrum disorder (ASD) is a neurodevelopmental disorder defined by persistent deficits in social functioning and the presence of restricted and repetitive behaviours (RRBs). RRBs refer to four subtypes of behaviour includi
Externí odkaz:
https://doaj.org/article/74dee1d6d46c4b2e953e8018c9efd17e
Autor:
Keana Loschiavo, Margie Danchin, Cheree Murrihy, Katrina Williams, Alexandra Ure, Mark Carter, Sarah Carlon, Robin P. Goin-Kochel, Kathleen L. Bagot, Jessica Kaufman
Publikováno v:
SSM: Qualitative Research in Health, Vol 2, Iss , Pp 100193- (2022)
Autistic children, adolescents and their younger siblings are less likely to be fully vaccinated compared to their peers in the general population. A focus on the influence of the unfounded link between the measles, mumps and rubella (MMR) vaccine an
Externí odkaz:
https://doaj.org/article/d2c7e6918b5940d297a32c5678073b32
Autor:
Rachael Knott, Beth P. Johnson, Jeggan Tiego, Olivia Mellahn, Amy Finlay, Kathryn Kallady, Maria Kouspos, Vishnu Priya Mohanakumar Sindhu, Ziarih Hawi, Aurina Arnatkeviciute, Tracey Chau, Dalia Maron, Emily-Clare Mercieca, Kirsten Furley, Katrina Harris, Katrina Williams, Alexandra Ure, Alex Fornito, Kylie Gray, David Coghill, Ann Nicholson, Dinh Phung, Eva Loth, Luke Mason, Declan Murphy, Jan Buitelaar, Mark A. Bellgrove
Publikováno v:
Molecular Autism, Vol 12, Iss 1, Pp 1-24 (2021)
Abstract Background ASD and ADHD are prevalent neurodevelopmental disorders that frequently co-occur and have strong evidence for a degree of shared genetic aetiology. Behavioural and neurocognitive heterogeneity in ASD and ADHD has hampered attempts
Externí odkaz:
https://doaj.org/article/40602d2099c14f7cbb70a6e3e590465b
Autor:
Emma K. Baker, Marta Arpone, Solange Aliaga Vera, Lesley Bretherton, Alexandra Ure, Claudine M. Kraan, Minh Bui, Ling Ling, David Francis, Matthew F. Hunter, Justine Elliott, Carolyn Rogers, Michael J. Field, Jonathan Cohen, Lorena Santa Maria, Victor Faundes, Bianca Curotto, Paulina Morales, Cesar Trigo, Isabel Salas, Angelica M. Alliende, David J. Amor, David E. Godler
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 11, Iss 1, Pp 1-15 (2019)
Abstract Background Fragile X syndrome (FXS) is a common cause of intellectual disability and autism spectrum disorder (ASD) usually associated with a CGG expansion, termed full mutation (FM: CGG ≥ 200), increased DNA methylation of the FMR1 promot
Externí odkaz:
https://doaj.org/article/e05c1a167cbd4ce9a6910a82c9dd4958
Publikováno v:
Journal of Autism and Developmental Disorders
This review aimed to assess the quality and content of recommendations for delivering an autism diagnosis, published internationally within clinical practice guidelines. Seventeen relevant guidelines were identified. When methodological information w
Publikováno v:
Review Journal of Autism and Developmental Disorders. 9:54-69
Autistic regression (AR) is commonly characterised as the loss of previously acquired language and social skills. This systematic review sought to identify studies that used family home videos to investigate early developmental patterns before AR ons
Autor:
Solange Aliaga Vera, Emma Baker, Víctor Faundes, Michael Field, Matthew F. Hunter, Minh Bui, Bianca Curotto, Isabel Salas, Ling Ling, Jonathan Cohen, Angelica M. Alliende, Lorena Santa María, Justine Elliott, Marta Arpone, Claudine Kraan, Alexandra Ure, Cesar Trigo, David J. Amor, David E. Godler, Carolyn Rogers, David Francis, Paulina Morales, Lesley Bretherton
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 11, Iss 1, Pp 1-15 (2019)
Journal of Neurodevelopmental Disorders
Journal of Neurodevelopmental Disorders
BackgroundFragile X syndrome (FXS) is a common cause of intellectual disability and autism spectrum disorder (ASD) usually associated with a CGG expansion, termed full mutation (FM: CGG ≥ 200), increased DNA methylation of theFMR1promoter and silen
Publikováno v:
Australian journal of general practice. 50(3)
Background In Australia, preschoolers are being identified and diagnosed as autistic. Objective The aim of this article is to describe the different paths preschool children and their families can take from identification of developmental or behaviou
Publikováno v:
Cochrane Database of Systematic Reviews.
Autor:
Dinh Phung, Amy Finlay, Kathryn Kallady, David Coghill, Ann E. Nicholson, Alexandra Ure, Kirsten Furley, Rachael Knott, Luke Mason, Katrina Williams, Maria Kouspos, Declan G. Murphy, Dalia N. Maron, Ziarih Hawi, Katrina Harris, Olivia J. Mellahn, Beth Patricia Johnson, Kylie Megan Gray, Tracey Chau, Emily Clare Mercieca, Eva Loth, Aurina Arnatkeviciute, Mark A. Bellgrove, Jeggan Tiego, Alex Fornito, Vishnu Priya Mohanakumar Sindhu, Jan K. Buitelaar
Publikováno v:
Molecular Autism
Molecular Autism, 12, 1
Molecular Autism, Vol 12, Iss 1, Pp 1-24 (2021)
Molecular Autism, 12
Molecular Autism, 12, 1
Molecular Autism, Vol 12, Iss 1, Pp 1-24 (2021)
Molecular Autism, 12
BackgroundASD and ADHD are prevalent neurodevelopmental disorders that frequently co-occur and have strong evidence for a degree of shared genetic aetiology. Behavioural and neurocognitive heterogeneity in ASD and ADHD has hampered attempts to map th