Parents' perceptions of the services provided to children with cerebral palsy in the transition from preschool rehabilitation to school-based services

Author:

Alsem M. W.1,Verhoef M.1,Gorter J. W.2,Langezaal L. C. M.1,Visser-Meily J. M. A.1,Ketelaar M.1

Affiliation:

1. Brain Centre Rudolf Magnus and Centre of Excellence for Rehabilitation Medicine, De Hoogstraat Rehabilitation; University Medical Centre Utrecht; Utrecht The Netherlands

2. Department of Pediatrics and CanChild Centre for Childhood Disability Research; McMaster University; Hamilton Canada

Funder

ZonMw, The Netherlands Organization for Health Research and Development

Johanna Kinderfonds

Bio Children Rehabilitation

Publisher

Wiley

Subject

Public Health, Environmental and Occupational Health,Developmental and Educational Psychology,Pediatrics, Perinatology and Child Health

Reference36 articles.

1. Assessment of family needs in children with physical disabilities: development of a family needs inventory;Alsem;Child: Care, Health and Development,2013

2. Parent-reported quality of life of children with cerebral palsy in Europe;Arnaud;Pediatrics,2008

3. What is the future of family outcomes and family-centered services?;Bailey;Topics in Early Childhood Special Education,2012

4. Family-centered theory: origins, development, barriers, and supports to implementation in rehabilitation medicine;Bamm;Archives of Physical Medicine and Rehabilitation,2008

5. Measure of Processes of Care (MPOC) applied to measure parent's perception of the habilitation process in Sweden;Bjerre;Child: Care, Health and Development,2004

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