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The following HTML text is provided to enhance online readability. Many aspects of typography translate only awkwardly to HTML. Please use the page image as the authoritative form to ensure accuracy. Vickers JL, Carlisle C. Choices and control: parental experiences in pediatric terminal home care. J Ped Onc Nursing 2000; 17:12–21. Weisman SJ. 1998. Supportive care in children with cancer. In: Principles and Practice of Supportive Oncology. Berger A, Portenoy RK, Weissman DE (eds). Philadelphia: Lippincott-Raven, pp. 845–52. Wessel MA. The role of the primary pediatrician when a child dies [editorial]. Arch Pediatr Adolesc Med 1998; 152:837–838. Whittam EH. Terminal care of the dying child: psychosocial implications of care. Cancer 1993; 71:3450–3462. WHO (World Health Organization) and International Association for the Study of Pain. 1998. Cancer Pain Relief and Palliative Care in Children. Geneva: World Health Organization. Wolfe J. Personal communication to Joanne Hilden, 2000. Wolfe J, Grier HE, Klar N, Salem-Schatz S, Emanuel EJ, Weeks JC. Physician-assisted suicide and euthanasia: experiences and attitudes among parents of children who have died of cancer. Proc ASCO 1999; 18:577a. Wolfe J, Grier HE, Klar N, Levin S, Ellenbogen J, Salem-Schatz S, Emanuel EJ, Weeks JC. Symptoms and suffering at the end of life in children with cancer. N Engl J Med 2000; 342:326–333. Yee JD, Berde CB. Dextroamphetamine or methylphenidate as adjuvants to opioid analgesia for adolescents with cancer. J Pain Sympt Manage 1994; 9:122–125.
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