Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Avril, Kennan"'
Autor:
Mengqi Li, Declan Devane, Claire Beecher, Maura Dowling, Austin G. Duffy, Caitriona Duggan, David Robert Grimes, Avril Kennan, Claire Kilty, Allen Nsangi, Andrew D. Oxman, Derek C. Stewart, Elaine Toomey, Marie Tierney
Publikováno v:
PEC Innovation, Vol 5, Iss , Pp 100311- (2024)
Objective: The overabundance of health misinformation has undermined people's capacity to make evidence-based, informed choices about their health. Using the Informed Health Choices (IHC) Key Concepts (KCs), we are developing a two-stage education pr
Externí odkaz:
https://doaj.org/article/77e666dcfffd429fb64fe8b21f11363e
Autor:
Robert O’Connor, Andrew D. Oxman, Marie Tierney, Claire Beecher, Derek C. Stewart, Mengqi Li, Caitriona Duggan, Austin G. Duffy, Maura Dowling, Avril Kennan, David Robert Grimes, Allen Nsangi, Declan Devane, Sarah McLoughlin, Elaine Toomey
Publikováno v:
HRB Open Research, Vol 5 (2022)
Background: Few areas of health have been as insidiously influenced by misinformation as cancer. Thus, interventions that can help people impacted by cancer reduce the extent to which they are victims of misinformation are necessary. The Informed Hea
Externí odkaz:
https://doaj.org/article/6d83dce25a0344fdb83ecbb0b7140f50
Autor:
Suja Somanadhan, Emma Nicholson, Emma Dorris, Aoife Brinkley, Avril Kennan, Eileen Treacy, Awan Atif, Sean Ennis, Vicky McGrath, Derick Mitchell, Grace O’Sullivan, Julie Power, Anne Lawlor, Paul Harkin, Sally Ann Lynch, Philip Watt, Avril Daly, Susie Donnelly, Thilo Kroll
Publikováno v:
HRB Open Research, Vol 3 (2020)
Background: Rare diseases are individually rare, but collectively these conditions are common. Research on rare diseases are currently focused on disease-specific needs rather than a life-course perspective. The Rare Disease Research Partnership (RAi
Externí odkaz:
https://doaj.org/article/e2283184ff8e4267ac1b5bd91ac24ffc
Publikováno v:
Acta Dermato-Venereologica, Vol 100, Iss 8, p adv00116 (2020)
Abstract is missing (Short communication)
Externí odkaz:
https://doaj.org/article/16da7c8dd7b044a49d9fd44b0cf9d723
Publikováno v:
Administration, Vol 69, Iss 3, Pp 1-18 (2021)
This paper offers a multi-perspective approach on the role of engaged research in health and social care. Each of the authors focuses on their individual experiences of this domain, from the perspective of an academic partner of the Health Research B
Autor:
Mengqi Li, Declan Devane, Claire Beecher, Austin G. Duffy, Caitriona Duggan, Maura Dowling, David Robert Grimes, Avril Kennan, Sarah McLoughlin, Allen Nsangi, Andrew D. Oxman, Robert O’Connor, Derek C. Stewart, Elaine Toomey, Marie Tierney
Publikováno v:
HRB Open Research. 5:55
Background: Few areas of health have been as insidiously influenced by misinformation as cancer. Thus, interventions that can help people impacted by cancer reduce the extent to which they are victims of misinformation are necessary. The Informed Hea
Autor:
Paul Harkin, Suja Somanadhan, Sean Ennis, Awan Atif, Emma R. Dorris, Avril Daly, Eileen P. Treacy, Julie Power, Sally Ann Lynch, Avril Kennan, Grace O’Sullivan, Susie Donnelly, Emma Nicholson, Anne Lawlor, Aoife Brinkley, Thilo Kroll, Derick Mitchell, Philip Watt, Vicky McGrath
Publikováno v:
HRB Open Research
Background: The Rare Disease Research Partnership (RAinDRoP) was established in 2018 to bring together a wide variety of diverse voices in the rare disease community in Ireland and form a research partnership. This approach enabled clinicians, patien
Publikováno v:
Acta Dermato-Venereologica, Vol 100, Iss 8, p adv00116 (2020)
is missing (Short communication)
Autor:
Emma Doris, Atif Awan, Suja Somanadhan, Sean Ennis, Derick Mitchell, Avril Kennan, Eileen P. Treacy, Sally Ann Lynch, Emma Nicholson, Aoife Brinkley, Thilo Kroll, Vicky Mc Garth
Publikováno v:
Abstracts.
Background To date, the rare disease research community is largely fragmented in Ireland without a coherent programmatic focus. All too often, priorities for research are decided by one group of stakeholders. The James Lind Alliance (JLA) model allow
Autor:
Paul Harkin, Emma R. Dorris, Derick Mitchell, Grace O’Sullivan, Julie Power, Anne Lawlor, Suja Somanadhan, Philip Watt, Sean Ennis, Sally Ann Lynch, Emma Nicholson, Avril Kennan, Vicky McGrath, Avril Daly, Susie Donnelly, Aoife Brinkley, Awan Atif, Thilo Kroll, Eileen P. Treacy
Publikováno v:
HRB Open Research. 3:13
Background: Rare diseases are individually rare, but collectively these conditions are common. Research on rare diseases are currently focused on disease-specific needs rather than a life-course perspective. The Rare Disease Research Partnership (RAi