Experiences of young adults with cerebral palsy in pediatric care transitioning to adult care
Aim To increase understanding regarding the experiences and values of young adults with cerebral palsy (CP), and their caregivers, regarding pediatric rehabilitation‐related care, including perceived barriers and potential facilitators to transition to adult care. Method This was a qualitative descr...
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Veröffentlicht in: | Developmental medicine and child neurology 2025-01, Vol.67 (1), p.99-110 |
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