Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jonathan Broomfield"'
Autor:
Hannah M. Worboys, Jonathan Broomfield, Aiden Smith, Rachael Stannard, Freya Tyrer, Elpida Vounzoulaki, Barbara Czyznikowska, Gurpreet Grewal-Santini, Justin Greenwood, Laura J. Gray
Publikováno v:
Research Involvement and Engagement, Vol 9, Iss 1, Pp 1-6 (2023)
Abstract Background Patient and Public Involvement and Engagement (PPIE) is important to all aspects of health research. However, there are few examples of successful PPIE in statistical methodology research. One of the reasons for this relates to ch
Externí odkaz:
https://doaj.org/article/2e290b1f6c194fc0b47947e204ae6cdd
Autor:
Lucy Abell, Francesca Maher, Samina Begum, Sarah Booth, Jonathan Broomfield, Sangyu Lee, Ellesha Smith, Rachael Stannard, Lucy Teece, Elpida Vounzoulaki, Hannah Worboys, Laura J. Gray
Publikováno v:
Research Involvement and Engagement, Vol 9, Iss 1, Pp 1-13 (2023)
Abstract Background Patient and public involvement (PPI) ensures that research is designed and conducted in a manner that is most beneficial to the individuals whom it will impact. It has an undisputed place in applied research and is required by man
Externí odkaz:
https://doaj.org/article/1cd6bbe373e545318aed69557c4a13b3
Autor:
Jonathan Broomfield, Keith Abrams, Nick Latimer, Michela Guglieri, Mark Rutherford, Michael Crowther
Publikováno v:
Brain and Behavior, Vol 13, Iss 12, Pp n/a-n/a (2023)
Abstract Background Duchenne muscular dystrophy (DMD) is a rare, muscle‐degenerative disease predominantly affecting males. Natural history models capture the full disease pathway under current care and combine with estimates of new interventions
Externí odkaz:
https://doaj.org/article/af8c1ccc94e14c8383f076690e267936
Autor:
Jonathan Broomfield, Micki Hill, Fleur Chandler, Michael Crowther, Josie Godfrey, Michela Guglieri, Jon Hastie, Jane Larkindale, Juliet Mumby-Croft, Emily Reuben, Fionn Woodcock, Keith Abrams
Background The aim of this study was to build a natural history model (NHM) for Duchenne muscular dystrophy (DMD) to provide new insights into the disease and to inform economic evaluations of new therapies. The study was conducted as part of Project
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae887417c29fe7a1e0231752049b6a81
https://doi.org/10.21203/rs.3.rs-2405860/v1
https://doi.org/10.21203/rs.3.rs-2405860/v1
Background and ObjectivesDuchenne muscular dystrophy (DMD) is a rare progressive disease that is often diagnosed in early childhood and leads to considerably reduced life expectancy; because of its rarity, research literature and patient numbers are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb7bd171811b35ce93b7aa4f8ceaab3d
http://wrap.warwick.ac.uk/160570/1/WRAP-life-expectancy-duchenne-muscular-dystrophy-Abrams-2021.pdf
http://wrap.warwick.ac.uk/160570/1/WRAP-life-expectancy-duchenne-muscular-dystrophy-Abrams-2021.pdf
Autor:
Clark Glasgow, Eunice Y C Lau, Luigi Aloj, Ines Harper, Heok Cheow, Tilak Das, Laurence Berman, Andrew S Powlson, Waiel A Bashari, Benjamin G Challis, Alison Marker, Penelope Moyle, Isra Ahmed Mohamed, Nadia Schoenmakers, Jonathan Broomfield, Sue Oddy, Carla Moran, Mark Gurnell, Piyush Jani, Liam Masterson, Brian Fish, Ruth T Casey
Publikováno v:
The Journal of clinical endocrinology and metabolism. 107(6)
Primary hyperparathyroidism (PHPT) is characterized by hypercalcemia driven by excess parathyroid hormone (PTH) secretion. PHPT is a common endocrine condition with a prevalence of 1 to 7 cases per 1000 adults. PHPT typically presents in the fifth or
Publikováno v:
SSRN Electronic Journal.
Background: Duchenne Muscular Dystrophy (DMD) is a rare progressive disease, which is often diagnosed in early childhood, and causes significantly reduced life expectancy. Due to its rarity, research literature and patient numbers are limited. To ful