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Research Papers

A qualitative exploration of the priorities and experiences of children with Duchenne muscular dystrophy, their parents, and healthcare professionals around weight management

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Pages 8234-8242 | Received 14 Aug 2020, Accepted 13 Nov 2021, Published online: 10 Dec 2021

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Madison L. Giles, Geoff D. C. Ball, Revi Bonder, Annick Buchholz, Jan Willem Gorter, Katherine M. Morrison, Arnaldo Perez, Meaghan Walker & Amy C. McPherson. (2023) Exploring the complexities of weight management care for children with spina bifida: a qualitative study with children and parents. Disability and Rehabilitation 0:0, pages 1-9.
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Articles from other publishers (2)

Philip A. Powell & Jill Carlton. (2022) A comprehensive qualitative framework for health-related quality of life in Duchenne muscular dystrophy. Quality of Life Research 32:1, pages 225-236.
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Charlotte Handberg, Ulla Werlauff & Ann-Lisbeth Højberg. (2022) Perspectives on Everyday Life Challenges of Danish Young People With Duchenne Muscular Dystrophy (DMD) on Corticosteroids. Global Qualitative Nursing Research 9, pages 233339362210948.
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