Zobrazeno 1 - 10
of 88
pro vyhledávání: '"Caroline Richards"'
Autor:
Rory O’Sullivan, Stacey Bissell, Georgie Agar, Jayne Spiller, Andrew Surtees, Mary Heald, Emma Clarkson, Aamina Khan, Christopher Oliver, Andrew P. Bagshaw, Caroline Richards
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 16, Iss 1, Pp 1-18 (2024)
Abstract Background Overactivity is prevalent in several rare genetic neurodevelopmental syndromes, including Smith-Magenis syndrome, Angelman syndrome, and tuberous sclerosis complex, although has been predominantly assessed using questionnaire tech
Externí odkaz:
https://doaj.org/article/f0d73da6a8414278be775542b1506da8
Publikováno v:
BMJ Open, Vol 14, Iss 7 (2024)
Introduction Preterm birth (
Externí odkaz:
https://doaj.org/article/e7682d9efdc946e99fe7a3ba06d2984b
Autor:
Emma L. Taylor, Paul A. Thompson, Nicholas Manktelow, Samantha Flynn, David Gillespie, Jill Bradshaw, Nick Gore, Ashley Liew, Mark Lovell, Kate Sutton, Caroline Richards, Stavros Petrou, Peter E. Langdon, Gemma Grant, Vivien Cooper, Kate Seers, Richard P. Hastings
Publikováno v:
BMC Health Services Research, Vol 23, Iss 1, Pp 1-13 (2023)
Abstract Background One in five children with an intellectual disability in the UK display behaviours that challenge. Despite associated impacts on the children themselves, their families, and services, little research has been published about how be
Externí odkaz:
https://doaj.org/article/77d8c4b59e9b44959827190364a3edd3
Autor:
Leandro Junges, Daniel Galvis, Alice Winsor, Grace Treadwell, Caroline Richards, Stefano Seri, Samuel Johnson, John R. Terry, Andrew P. Bagshaw
Publikováno v:
PLoS ONE, Vol 19, Iss 8 (2024)
Externí odkaz:
https://doaj.org/article/b4248db03e1c4061afdade5fe02f2cbe
Autor:
Jessica A. Martin, Kathryn Robertson, Caroline Richards, Gaia Scerif, Kate Baker, Charlotte Tye
Publikováno v:
BMC Psychology, Vol 11, Iss 1, Pp 1-14 (2023)
Abstract Background The Coronavirus disease 2019 (COVID-19) pandemic has impacted parental and child mental health and wellbeing in the UK. This study aimed to explore the experiences of parents of children with rare neurological and neurodevelopment
Externí odkaz:
https://doaj.org/article/bf4443f0ed734958bd5336c240d42f1f
Autor:
Victoria Newell, Lucy Phillips, Chris Jones, Ellen Townsend, Caroline Richards, Sarah Cassidy
Publikováno v:
Molecular Autism, Vol 14, Iss 1, Pp 1-37 (2023)
Abstract Background Suicidality is highly prevalent in autistic people without co-occurring intellectual disabilities, and high autistic traits are found in adults who have attempted suicide. However, prevalence rates for both autistic and possibly a
Externí odkaz:
https://doaj.org/article/dc03cbd784d94ab684440d5e7dc063fb
Autor:
Natali Bozhilova, Alice Welham, Dawn Adams, Stacey Bissell, Hilgo Bruining, Hayley Crawford, Kate Eden, Lisa Nelson, Christopher Oliver, Laurie Powis, Caroline Richards, Jane Waite, Peter Watson, Hefin Rhys, Lucy Wilde, Kate Woodcock, Joanna Moss
Publikováno v:
Molecular Autism, Vol 14, Iss 1, Pp 1-14 (2023)
Abstract Background Phenotypic studies have identified distinct patterns of autistic characteristics in genetic syndromes associated with intellectual disability (ID), leading to diagnostic uncertainty and compromised access to autism-related support
Externí odkaz:
https://doaj.org/article/fce28d31c5f244df9e6075e9714859a7
Autor:
Andrea T. Thomas, Jane Waite, Caitlin A. Williams, Jeremy Kirk, Chris Oliver, Caroline Richards
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 14, Iss 1, Pp 1-20 (2022)
Abstract Background CHARGE syndrome (OMIM #214800) is a phenotypically complex genetic condition characterised by multi-system, multi-sensory impairments. Behavioural, psychological, cognitive and sleep difficulties are not well delineated and are li
Externí odkaz:
https://doaj.org/article/6587504f234e4bd99750a69f71891cae
Autor:
Stacey Bissell, Chris Oliver, Joanna Moss, Mary Heald, Jane Waite, Hayley Crawford, Vishakha Kothari, Lauren Rumbellow, Grace Walters, Caroline Richards
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 14, Iss 1, Pp 1-21 (2022)
Abstract Background SATB2-associated syndrome (SAS) is a multisystem neurodevelopmental disorder characterised by intellectual disability, speech delay, and craniofacial anomalies. Although the clinical presentation of SAS is well-delineated, behavio
Externí odkaz:
https://doaj.org/article/22db677fdc524bed9a6c6cc527932147
Autor:
Georgie Agar, Stacey Bissell, Lucy Wilde, Nigel Over, Caitlin Williams, Caroline Richards, Chris Oliver
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-15 (2022)
Abstract Background Smith–Magenis syndrome (SMS) is a rare genetic syndrome associated with a unique profile of early morning waking and daytime sleepiness. Children with SMS evidence high rates of self-injury and aggression and have a preference f
Externí odkaz:
https://doaj.org/article/4f07f2373ce5487fab4cffa8322b407c