Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Mary Heald"'
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
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:
Alice Watkins, Stacey Bissell, Jo Moss, Chris Oliver, Jill Clayton-Smith, Lorraine Haye, Mary Heald, Alice Welham
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 11, Iss 1, Pp 1-15 (2019)
Abstract Background Pitt-Hopkins syndrome (PTHS) is a genetic neurodevelopmental disorder associated with intellectual disability. Although the genetic mechanisms underlying the disorder have been identified, description of its behavioural phenotype
Externí odkaz:
https://doaj.org/article/87f998934ac54d62a20a80c08c1d4c05
Publikováno v:
Frontiers in Behavioral Neuroscience, Vol 15 (2021)
Angelman syndrome (AS) is caused by loss of information from the 15q11.2-13 region on the maternal chromosome with striking phenotypic difference from Prader–Willi syndrome in which information is lost from the same region on the paternal chromosom
Externí odkaz:
https://doaj.org/article/fdc814d52d894405addf199e6fda9d55
Autor:
Jayne Trickett, Chris Oliver, Mary Heald, Hayley Denyer, Andrew Surtees, Emma Clarkson, Paul Gringras, Caroline Richards
Publikováno v:
Frontiers in Psychiatry, Vol 10 (2019)
Objectives: To assess sleep quality and timing in children with Angelman syndrome (AS) with sleep problems using questionnaires and actigraphy and contrast sleep parameters to those of typically developing (TD) children matched for age and sex.Method
Externí odkaz:
https://doaj.org/article/6fdb3ab1e55c4c2f9932c00ad98c1c89
Autor:
Mary Heald, Kate Woodcock, Caroline Richards, Joanna Moss, Chris Oliver, Hayley Crawford, Jane Waite, Debbie Allen, Alice Welham, Lucy Wilde, Dawn Adams
Publikováno v:
Paediatrics and Child Health. 30:416-424
Children and adults with severe intellectual disability and complex needs often show behaviours and distress that carers and professionals find difficult to identify causes for, manage and decrease. The prevailing view is that these behaviours and di
Autor:
Chris Oliver, Katherine Ellis, Georgie Agar, Stacey Bissell, Justin Cheuk Yin Chung, Hayley Crawford, Effie Pearson, Kelly Wade, Jane Waite, Debbie Allen, Lucy Deeprose, Georgina Edwards, Lauren Jenner, Breanne Kearney, Lauren Shelley, Kayla Smith, Hayley Trower, Dawn Adams, Louise Daniel, Laura Groves, Mary Heald, Jo Moss, Caroline Richards, Rachel Royston, Joanne Tarver, Alice Welham, Lucy Wilde, Kate Woodcock
Publikováno v:
Contemporary Issues in Evaluating Treatment Outcomes in Neurodevelopmental Disorders ISBN: 9780323988834
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e952a66a49a0eadef58ad1adc3963576
https://doi.org/10.1016/bs.irrdd.2022.05.004
https://doi.org/10.1016/bs.irrdd.2022.05.004
Publikováno v:
Journal of Intellectual Disability Research. 64:117-130
Background: There is growing evidence to suggest that children with neurodevelopmental disorders may evidence differences in their sensory processing. The aim of this study was to compare sensory processing patterns in three genetic syndromes associa
Autor:
Emily Goodman, Joanna Moss, Mary Heald, Effie Pearson, Sotaro Kita, Olivia Massey, Lucy Wilde, Chris Oliver
Publikováno v:
Journal of Intellectual Disability Research. 63:1078-1085
Publikováno v:
Frontiers in Behavioral Neuroscience, Vol 15 (2021)
Frontiers in Behavioral Neuroscience
Frontiers in Behavioral Neuroscience
Angelman syndrome (AS) is caused by loss of information from the 15q11.2-13 region on the maternal chromosome with striking phenotypic difference from Prader–Willi syndrome in which information is lost from the same region on the paternal chromosom