Community-based disability services in the USA: A paediatric perspective

Lancet

Volumn 354, Issue 9180, 1999, Pages 761-762

  Kaplan, Lawrence C ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; CHILD; CHILD CARE; COMMUNITY CARE; DISABILITY; HEALTH CARE ACCESS; HEALTH CARE AVAILABILITY; HEALTH CARE COST; HEALTH CARE PLANNING; HUMAN; PRIMARY MEDICAL CARE; PRIORITY JOURNAL; SHORT SURVEY; UNITED STATES;

EID: 0033612872     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(99)06141-3     Document Type: Short Survey

References (6)

1. Perrin E.C., Newacheck P., Pless I.et al. Issues involved in the definition and classification of chronic health conditions. Pediatrics. 91:1993;787-793.
2. Division of Services for Children with Special Health Care Needs. Children with special health care needs in managed care organizations: definitions and identification, family participation, capitation, and risk adjustment, quality of care - summary of expert work group meetings. Rocville MD: Maternal and Child Health Bureau, US Department of Health and Human Services, 1996.
3. Mulik J.A., Pueschel S.M. Parent-professional partnership in developmental disability services. 1983;Ware Press, Cambridge, MA.
4. Butler C., Chambers H., Goldstein M.et al. Evaluating research in developmental disabilities: a conceptual framework for reviewing treatment outcomes. Dev Med Child Neurol. 41:1999;55-59.
5. Ireys H., Nelson R. New federal policy for children with special health care needs: implications for pediatricians. Pediatrics. 90:1992;321-327.
6. Wells N., Anderson B. Families in program and policy: report of a 1992 survey of family participation in state Title V programs for children with special health care needs. Boston: CAPP National Parent Resource Center, Federation for Children With Special Needs, 1993.