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Aim
This longitudinal study examined what perceptions paediatric patients with cerebral palsy (CP) and their caregivers had of the patient's quality of life (QoL). It examined changing trends as children with CP became adolescents and examined the feasibility of the Finnish version of the CP QOL‐Teen questionnaire.
Methods
Carried out in autumn 2015, this study formed part of the multi‐centre Finnish...
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