Abrahao R et al., A qualitative study of barriers and facilitators to adolescents and young adults' participation in cancer clinical trials: Oncologist and patient perspectives.
Atwiine B et al., "Money was the problem": Caregivers' self-reported reasons for abandoning their children's cancer treatment in southwest Uganda.
Bates C et al., Psychosocial functioning of caregivers of pediatric brain tumor survivors.
Bisogno G et al., Role of centers with different patient volumes in the management of rhabdomyosarcoma. An analysis by the Italian Pediatric Soft Tissue Sarcoma Committee.
Bouchard E et al., Social media use and patient-provider relationships: Lessons for patients, caregivers, and healthcare providers.
Brosnan P et al., Psychosocial care providers' perspectives: Barriers to implementing services for siblings of children with cancer.
Canter K et al., A community-based trial of a psychosocial eHealth intervention for parents of children with cancer.
Cowfer B et al., Effect of time on quality of parent-child communication in pediatric cancer.
De Abreu Lourenco R et al., Understanding decisions to participate in genomic medicine in children's cancer care: A comparison of what influences parents, health care providers, and the general community.
Etkin-Spigelman L et al., Sharing psychosocial risk screening information with pediatric oncology healthcare providers: Service utilization and related factors.
Fardell J et al., Long-term health-related quality of life in young childhood cancer survivors and their parents.
Fleming C et al., Poor diet quality and adverse eating behaviors in young survivors of childhood cancer.
Greenzang K et al., Thinking ahead: Parents' worries about late effects of childhood cancer treatment.
Hancock K et al., A qualitative examination of the benefits and challenges of a psychosocial screening intervention in pediatric oncology: "Support comes to us".
Hjelmstedt S et al., Facilitators and barriers to return to work and meet financial needs in parents of children with cancer.
Iveus K et al., Family bonding as a result of the family talk intervention in pediatric oncology: Siblings' experiences.
Levitch C et al., Comparison of neuropsychological functioning in pediatric posterior fossa tumor survivors: Medulloblastoma, low-grade astrocytoma, and healthy controls.
McCarthy M et al., Parental adjustment following their child's completion of acute lymphoblastic leukemia treatment
Meryk A et al., Implementation of daily patient-reported outcome measurements to support children with cancer.
Moola F et al., Contemplating art and identity during a research study: Reflections on working with a youth with cancer.
Moscato E et al., Family functioning and adaptation following pediatric brain tumor: A systematic review.
Mueller E et al., The practical matters of including patient-reported outcomes in pediatric oncology clinical care.
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Phillips C et al., Implementation science in pediatric oncology: A narrative review and future directions.
Posa S et al., Exploring illness identity among children and youth living with cancer: A narrative review.
Schaefer M et al., "Giving the gift of life twice": Understanding the lived experiences of parent donors and nondonors in pediatric haploidentical hematopoietic cell transplantation.
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Szilagyi C et al., Interprofessional spiritual care education in pediatric hematology-oncology: A pilot study.
Warner E et al., Cancer content and social media platform influence young adult cancer caregivers' social support on social media
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Purrezaian M et al., Group psychodrama for children with leukemia: A brief report.
Barrera M et al., Pilot randomized psychosocial trial of a screening intervention in pediatric oncology.
Christensen S et al., From well-known to changed everyday family life in families with childhood cancer: A grounded theory of disrupted family dynamic.
Cuffe R et al., Age-stratified distress thermometers with Worry and Learning problem domains for the paediatric oncology population: Development and validation.
Danhauer S et al., Stakeholder-informed conceptual framework for financial burden among adolescents and young adults with cancer.
Herzog K et al., Illness perceptions in patients and parents in paediatric oncology during acute treatment and follow-up care.
Jones A et al., The toll of transition: Caregiver perceptions of family adjustment during the transition off pediatric cancer therapy.
Klages K et al., Health-related quality of life, obesity, fragmented sleep, fatigue, and psychosocial problems among youth with craniopharyngioma.
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Slaughter R et al., Acculturation discrepancy and mental health associations among Hispanic childhood cancer survivors and their parents.
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