A systematic review and qualitative synthesis of the experiences of parents of individuals living with Duchenne muscular dystrophy
Author:
Affiliation:
1. Department of Psychology, Queen’s University Belfast, Belfast, Northern Ireland
2. MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology, National Hospital for Neurology and Neurosurgery, London, UK
Funder
NIHR Biomedical Research Centre at UCLH.
Publisher
Informa UK Limited
Subject
Rehabilitation
Link
https://www.tandfonline.com/doi/pdf/10.1080/09638288.2022.2060336
Reference68 articles.
1. Duchenne and Becker muscular dystrophy in adolescents: current perspectives
2. The burden, epidemiology, costs and treatment for Duchenne muscular dystrophy: an evidence review
3. A review of quality of life themes in Duchenne muscular dystrophy for patients and carers
4. Predictors of Health-Related Quality of Life in boys with Duchenne muscular dystrophy from six European countries
5. Diagnosis and management of Duchenne muscular dystrophy, part 3: primary care, emergency management, psychosocial care, and transitions of care across the lifespan
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1. Factors Associated With Early Motor Function Trajectories in DMD After Glucocorticoid Initiation;Neurology;2024-05-28
2. “You Take This Day by Day, Come What May”: A Qualitative Study of the Psychosocial Impacts of Living with Duchenne Muscular Dystrophy;Advances in Therapy;2024-05-06
3. Assessing the Benefits and Harms Associated with Early Diagnosis from the Perspective of Parents with Multiple Children Diagnosed with Duchenne Muscular Dystrophy;International Journal of Neonatal Screening;2024-04-15
4. Young Adults and Parents’ Coping With Duchenne/Becker Muscular Dystrophy: A Focus Group Study;Emerging Adulthood;2024-03-26
5. Economic Evaluations of Treatments for Duchenne Muscular Dystrophy: The Caregiver QALY Trap;PharmacoEconomics;2024-03-05
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