Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Suzanne M. Nevin"'
Autor:
Suzanne M. Nevin, Brittany C. McGill, Lauren Kelada, Gail Hilton, Megan Maack, Kristina L. Elvidge, Michelle A. Farrar, Gareth Baynam, Naomi T. Katz, Leigh Donovan, Sarah Grattan, Christina Signorelli, Kaustuv Bhattacharya, Kenneth Nunn, Claire E. Wakefield
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-32 (2023)
Abstract Background Childhood dementias are a group of rare and ultra-rare paediatric conditions clinically characterised by enduring global decline in central nervous system function, associated with a progressive loss of developmentally acquired sk
Externí odkaz:
https://doaj.org/article/7c83512c4cb844e78874ff664fe56e6c
Autor:
Suzanne M. Nevin, Claire E. Wakefield, Ann Dadich, Fleur LeMarne, Rebecca Macintosh, Erin Beavis, Rani Sachdev, Ann Bye, Kenneth Nunn, Elizabeth E. Palmer
Publikováno v:
PEC Innovation, Vol 1, Iss , Pp 100014- (2022)
Objective: To understand parents' of children with developmental and epileptic encephalopathies needs and preferences for psychological resources. Methods: Using a person-based approach, a multidisciplinary panel of clinician and researchers (n = 9)
Externí odkaz:
https://doaj.org/article/fb656a0c8d884597b7d2d91ffcd2bb03
Autor:
Suzanne M. Nevin, Lenny R. Vartanian
Publikováno v:
Journal of Eating Disorders, Vol 5, Iss 1, Pp 1-10 (2017)
Abstract Background Although the stigma of eating disorders such as anorexia has been well established, little is known about the social consequences of “clean dieting” and orthorexia nervosa. In two studies, we examined the social stigma of clea
Externí odkaz:
https://doaj.org/article/abdccc5c640149db8936d20d5dfc8f38
Autor:
Stephanie Best, Elizabeth E Palmer, Lauren Kelada, Rani Sachdev, Eden G Robertson, I Goranitis, Natalie Grainger, Fleur Le Marne, Kristine Pierce, Suzanne M Nevin, Rebecca Macintosh, Erin Beavis, Annie Bye
Publikováno v:
BMJ Open, Vol 12, Iss 10 (2022)
Introduction Developmental and epileptic encephalopathies (DEEs) are rare epilepsy conditions that collectively impact 1 in 2000 children. They are highly genetically heterogeneous, resulting in significant barriers to accurate and adequate informati
Externí odkaz:
https://doaj.org/article/eeb167524d8c4a76ac03283cc48a346f
Autor:
Elizabeth E Palmer, Rani Sachdev, Erin Beavis, Rebecca Macintosh, Fleur A Le Marne, Suzanne M Nevin, Ann ME Bye, Kenneth Nunn
Publikováno v:
Journal of Paediatrics and Child Health. 58:1718-1721
This is the first of three articles exploring the aspects of clinical care for children with rare neurological disorders including uncertainties old and new. The disruptive technologies of genomic sequencing and advanced therapeutics such as gene-bas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b352541aa05013a34dbf79e138e54a7
https://doi.org/10.1111/jpc.16165
https://doi.org/10.1111/jpc.16165
Publikováno v:
Genetics in Medicine. 24:535-548
Purpose Genetic testing is frequently conducted on people with intellectual disability. This systematic literature review sought to assess what research has been conducted with people with intellectual disability to investigate their opinions and exp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::577f5476f6a91e454a2a92572f99186e
https://doi.org/10.1016/j.gim.2021.11.013
https://doi.org/10.1016/j.gim.2021.11.013
Autor:
Elizabeth E. Palmer, Brittany C. McGill, Ann M. E. Bye, Kristine Barlow-Stewart, Claire E. Wakefield, Suzanne M. Nevin
Publikováno v:
Developmental Medicine & Child Neurology. 64:95-104
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08d50001527b5884553a8a49fd30e179
https://doi.org/10.1111/dmcn.14971
https://doi.org/10.1111/dmcn.14971
Autor:
Suzanne M Nevin, Erin Beavis, Rebecca Macintosh, Elizabeth E Palmer, Rani Sachdev, Fleur A Le Marne, Ann ME Bye, Kenneth Nunn
Publikováno v:
Journal of paediatrics and child healthReferences. 58(10)
This is the second of a three-part series that explores different aspects of uncertainty, certainty and hope in the context of providing clinical care for children with rare and life-limiting neurological disorders. When caring for families impacted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb2de77fa5064cb7482e924306605551
https://pubmed.ncbi.nlm.nih.gov/36069627
https://pubmed.ncbi.nlm.nih.gov/36069627
Autor:
Ann ME Bye, Fleur A Le Marne, Erin Beavis, Rebecca Macintosh, Suzanne M Nevin, Elizabeth E Palmer, Rani Sachdev, Kenneth Nunn
Publikováno v:
Journal of paediatrics and child healthReferences. 58(10)
This is the third article of a three-part series and addresses how clinicians provide hopefulness meaningfully to families coping with life-limiting and quality of life impairing neurological conditions. The first two articles addressed the enormous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74267c5cef40cdf7da5c4eeac07f4def
https://pubmed.ncbi.nlm.nih.gov/36062939
https://pubmed.ncbi.nlm.nih.gov/36062939
Publikováno v:
J Pediatr Genet
Genomics is rapidly being integrated into the routine care of children and families living with renal disease, principally as a diagnostic tool but also to direct therapy, identify at-risk relatives, and facilitate family planning. However, despite s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b032437f9e159d70df317f31fb71556
https://doi.org/10.1055/s-0040-1721439
https://doi.org/10.1055/s-0040-1721439