215 results on '"Kang, Tammy I."'
Search Results
2. Pediatric Palliative Care Parents’ Distress, Financial Difficulty, and Child Symptoms
3. Household material hardship and distress among parents of children with advanced cancer: A report from the PediQUEST Response trial
4. Program Development
5. The evolution of regret: decision-making for parents of children with cancer
6. Palliative Care in Adolescents and Young Adults with Special Healthcare Needs
7. Inclusion of children in the initial conversation about their cancer diagnosis: impact on parent experiences of the communication process
8. Tumor Talk and Child Well-Being: Perceptions of “Good” and “Bad” News Among Parents of Children With Advanced Cancer
9. Feasibility of Conducting a Palliative Care Randomized Controlled Trial in Children With Advanced Cancer: Assessment of the PediQUEST Study
10. Pediatric Exposure to Opioid and Sedation Medications during Terminal Hospitalizations in the United States, 2007-2011
11. Compassionate Discharges From the PICU: [RETRACTED]
12. Intended and unintended consequences: Ethics, communication, and prognostic disclosure in pediatric oncology
13. Goals of Care Among Parents of Children Receiving Palliative Care.
14. Prognostic disclosures over time: Parental preferences and physician practices
15. Disparities in prognosis communication among parents of children with cancer: The impact of race and ethnicity
16. Carboplatin Rechallenge After Hypersensitivity Reactions in Pediatric Patients With Low-Grade Glioma
17. Predictors of antiemetic alteration in pediatric acute myeloid leukemia
18. Shifting place of death among children with complex chronic conditions in the United States, 1989-2003
19. The Management of Pain in Children with Life-limiting Illnesses
20. Psychosocial and Spiritual Needs of Children Living with a Life-Limiting Illness
21. The use of palliative chemotherapy in pediatric oncology patients: A national survey of pediatric oncologists
22. Complementary and alternative therapy use in pediatric oncology patients with failure of frontline chemotherapy
23. Care experiences that foster trust between parents and physicians of children with cancer
24. Racial and Ethnic Differences in Parental Decision-Making Roles in Pediatric Oncology
25. Parental Hopeful Patterns of Thinking, Emotions, and Pediatric Palliative Care Decision Making: A Prospective Cohort Study
26. Partners in Pediatric Palliative Care: A Program to Enhance Collaboration Between Hospital and Community Palliative Care Services
27. The Relationship Between Household Income and Patient-Reported Symptom Distress and Quality of Life in Children With Advanced Cancer: A Report From the PediQUEST Study
28. The evolution of regret: decision-making for parents of children with cancer
29. Decisional burden among parents of children with cancer
30. Parental distress and desire for information regarding long‐term implications of pediatric cancer treatment
31. Self-reported fatigue in children with advanced cancer: Results of the PediQUEST study
32. The relationship between household income and patient‐reported symptom distress and quality of life in children with advanced cancer: A report from the PediQUEST study
33. Supporting Caregivers of Patients With Cancer: A Summary of Technology-Mediated Interventions and Future Directions
34. Impact of Natural Disasters on Children Receiving Palliative Care Lessons Learned from Hurricane Harvey
35. Reply to Cross-cultural communication in pediatric oncology: Catch them when they're young
36. Sources of parental hope in pediatric oncology
37. How Parents of Children With Cancer Learn About Their Children’s Prognosis
38. Intended and unintended consequences: Ethics, communication, and prognostic disclosure in pediatric oncology
39. Longitudinal parental preferences for late effects communication during cancer treatment
40. Disparities in prognosis communication among parents of children with cancer: The impact of race and ethnicity.
41. Decisional Regret Among Parents of Children With Cancer
42. Parents’ understanding of the risk of late effects of pediatric cancer therapy.
43. Palliative care in pediatric patients with hematologic malignancies
44. Psychological Well-Being and Family Environment of Siblings of Children with Life Threatening Illness
45. Intended and unintended consequences: Ethics, communication, and prognostic disclosure in pediatric oncology.
46. Carboplatin Rechallenge After Hypersensitivity Reactions in Pediatric Patients With Low‐Grade Glioma
47. Symptoms and Distress in Children With Advanced Cancer: Prospective Patient-Reported Outcomes From the PediQUEST Study
48. Longitudinal parental preferences for late effects communication during cancer treatment.
49. Good-Parent Beliefs of Parents of Seriously Ill Children
50. Caring for the Infant With Trisomy 18
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