Anderson, B. J., & Coyne, J. C. (1991). “Miscarried helping” in the families of children and adolescents with chronic disease. In J. H. Johnson & S. B. Johnson (Eds.), Advances in child health psychology (pp. 166–177). Gainesville: University of Florida Press.
Barakat, L. P., & Kazak A. E. (1999). Family issues. In R. T. Brown (Ed.), Cognitive aspects of chronic illness in children (pp. 333–354). New York: Guilford.
Bronfenbrenner, U. (1979). The ecology of human development. Cambridge, MA: Harvard University Press.
Brown, R. T. (2002). Society of pediatric psychology presidential address: Toward a social ecology of pediatric psychology. Journal of Pediatric Psychology, 27, 191–201.
Brown, R. T., Boeving, A., LaRosa, A., & Carpenter, L. A. (2006). Health and chronic illness. In D. A. Wolfe & E. J. Mash (Eds.), Behavioral and emotional disorders in adolescents: Nature, assessment, and treatment (pp. 505–531). New York: Guilford Press.
Carlson, C., Kubiszyn, T., & Guli, L. (2004). Consultation with caregivers and families. In R. T. Brown & N. J. Mahwah (Eds.). Handbook of pediatric psychology in school settings (pp. 617–635). New Jersey: Lawrence Erlbaum.
Drotar, D. (1997). Relating parent and family functioning to the psychological adjustment of children with chronic health conditions: What have we learned? What do we need to know? Journal of Pediatric Psychology, 22, 149–165.
Drotar, D. (2006). Theoretical models and frameworks for psychological intervention. In D. Drotar (Ed.), Psychological interventions in childhood chronic illness (pp. 33–55). Washington, DC: American Psychological Association.
Eiser, C., & Berrenberg, J. L. (1995). Assessing the impact of chronic disease on the relationship between parents and their adolescents. Journal of Psychosomatic Research, 39, 109–114.
Finkelstein, J. W. (1993). Familial influences on adolescent health. In R. M. Lerner (Ed.), Early adolescence: Perspective on research, policy, and intervention (pp. 11–126). New Jersey: Lawrence Erlbaum.
Hanson, C. L., Henggeler, S. W., & Burghen, G. A. (1987). Model of associations between psychological variables and health outcome measures of adolescents with IDDM. Diabetes Care, 10, 752–758.
Hoffman, R. G., Rodriguez, J. R., Andres, J. M., & Novak, D. A. (1995). Moderating effects of family functioning on the social adjustment of children with liver disease. Children’s Health Care, 24, 107–117.
Holden, E., Chmielewski, D., Nelson, C., & Kager, V. (1997). Controlling for general and disease-effects in child and family adjustments to chronic illness. Journal of Pediatric Psychology, 22, 15–27.
Kazak, A. (1989). Families of chronically ill children: A systems and social ecological model of adaptation and challenge. Journal of Consulting and Clinical Psychology, 57, 25–30.
Kazak, A. E., McClure, K. S., Alderfer, M. A., Hwang, W. T., Crump, T. A., Le, L. T., et al. (2004). Cancer-related parental beliefs: The Family Illness Beliefs Inventory (FIBI). Journal of Pediatric Psychology, 29, 531–542.
Kazak, A. E., Rourke, M. T., & Crump, T. A. (2003). Families and other systems in pediatric psychology. In M. C. Roberts (Ed.), Handbook of pediatric psychology (3rd ed., pp. 159–175). New York: Guilford Press.
Lewis, M., & Vitulano, L. A. (2003). Biopsychosocial issues and risk factors in the family when the child has a chronic illness. Child and Adolescent Psychiatric Clinics of North America, 12, 398–399.
Mayes, S. D., Handford, H. A., Kowalski, C., & Schaefer, J. H. (1988). Parent attitudes and child personality traits in hemophilia: A six-year longitudinal study. International Journal of Psychiatry in Medicine, 18, 339–355.
McCubbin, H. I., McCubbin, M. A., Patterson, J. M., Cauble, A. E., Wilson, L. R., & Warwick, W. (1983). CHIP – Coping Health Inventory for Parents: An assessment of parental coping patterns in the care of the chronically ill child. Journal of Marriage and the Family, 45, 359–370.
Northam, E., Anderson, P., Adler, R., Werther, G., & Warne, G. (1996). Psychosocial and family functioning in children with insulin-dependent diabetes at diagnosis and one year later. Journal of Pediatric Psychology, 21, 699–717.
Salewski, C. (2003). Illness representations in families with a chronically ill adolescent: Differences between family members and impact on patients’ outcome variables. Journal of Health Psychology, 8, 587–598.