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Articles

Development and preliminary validation of the challenges of living with cystic fibrosis (CLCF) questionnaire: a 46-item measure of treatment burden for parent/carers of children with CF

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Pages 1309-1344 | Received 28 Sep 2020, Accepted 28 Nov 2021, Published online: 08 Mar 2022

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Whitney Nesser, Eun-Hye Grace Yi, Amy J. Wotring, Matthew D. Hutchins & Scott Snyder. (2023) A Partial Picture, Without a Frame: Measuring Quality of Life in Cystic Fibrosis Caregivers. American Journal of Health Education 54:3, pages 233-241.
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Catherine O’Leary, Vivien Edwards, Katherine A Hardcastle, Anna McCulloch & Jamie M Duckers. (2022) Adverse Childhood Experiences (ACEs) in Adults with Cystic Fibrosis. Psychology Research and Behavior Management 15, pages 1601-1605.
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