scholarly article | Q13442814 |
P50 | author | Eduardo Bruera | Q60386359 |
P2093 | author name string | Donna S Zhukovsky | |
Gary B Chisholm | |||
Robert J Wells | |||
Marlene Z Cohen | |||
Cathy L Rozmus | |||
Rhonda S Robert | |||
Julio A Allo | |||
P2860 | cites work | A systematic review of symptom assessment scales in children with cancer | Q26849572 |
Cancer treatment and survivorship statistics, 2012 | Q27020961 | ||
Systematic review of psychosocial morbidities among bereaved parents of children with cancer | Q30224918 | ||
Symptoms and suffering at the end of life in children with cancer | Q33828342 | ||
Psychological distress in parents of children with advanced cancer | Q34678550 | ||
Judging the quality of care at the end of life: can proxies provide reliable information? | Q34999633 | ||
Levels of symptom burden during chemotherapy for advanced lung cancer: differences between public hospitals and a tertiary cancer center. | Q35112327 | ||
Cancer pain management and the JCAHO's pain standards: an institutional challenge | Q35143391 | ||
Symptom experiences of children and adolescents with cancer. | Q35177068 | ||
Instrument translation process: a methods review | Q35888382 | ||
Pain intensity assessment by bedside nurses and palliative care consultants: a retrospective study | Q35916428 | ||
A review of qualitative research on the childhood cancer experience from the perspective of siblings: a need to give them a voice. | Q36282720 | ||
Ethnicity and persistent symptom burden in breast cancer survivors | Q36854840 | ||
Talking About Cancer and Meeting Peer Survivors: Social Information Needs of Adolescents and Young Adults Diagnosed with Cancer | Q36933596 | ||
Literature review of methods to translate health-related quality of life questionnaires for use in multinational clinical trials | Q37052208 | ||
Health-related quality of life of adolescent and young adult patients with cancer in the United States: the Adolescent and Young Adult Health Outcomes and Patient Experience study | Q37065829 | ||
The impact of palliative care consultation on symptom assessment, communication needs, and palliative interventions in pediatric patients with cancer | Q37425237 | ||
Item-level informant discrepancies between children and their parents on the PROMIS(®) pediatric scales. | Q37452126 | ||
"Now that you mention it, doctor ... ": symptom reporting and the need for systematic questioning in a specialist palliative care unit | Q37470612 | ||
Multiple symptoms in pediatric oncology patients: a systematic review | Q37581325 | ||
Improving the care of children with advanced cancer by using an electronic patient-reported feedback intervention: results from the PediQUEST randomized controlled trial | Q37673195 | ||
Identifying determinants of quality of life of children with cancer and childhood cancer survivors: a systematic review | Q37879602 | ||
Review of symptom experiences in children and adolescents with cancer | Q37901330 | ||
Attitudes and practices among pediatric oncologists regarding end-of-life care: results of the 1998 American Society of Clinical Oncology survey | Q39555305 | ||
Trajectory of performance status and symptom scores for patients with cancer during the last six months of life. | Q39785424 | ||
The measurement of symptoms in young children with cancer: the validation of the Memorial Symptom Assessment Scale in children aged 7-12. | Q40667705 | ||
The measurement of symptoms in children with cancer. | Q40759632 | ||
Symptom evaluation in palliative medicine: patient report vs systematic assessment | Q42677550 | ||
The Pediatric Cancer Quality of Life Inventory (PCQL). I. Instrument development, descriptive statistics, and cross-informant variance | Q46301202 | ||
Symptom assessment in pediatric oncology: how should concordance between children's and parents' reports be evaluated? | Q46495681 | ||
Priorities, barriers and facilitators for remote support of cancer symptoms: a survey of Canadian oncology nurses. | Q46504921 | ||
How siblings of pediatric cancer patients experience the first time after diagnosis: a qualitative study | Q46951031 | ||
Communication in palliative medicine: a pilot study of a problem list to capture complex medical information | Q47905070 | ||
Impact of a half-day multidisciplinary symptom control and palliative care outpatient clinic in a comprehensive cancer center on recommendations, symptom intensity, and patient satisfaction: a retrospective descriptive study | Q48591782 | ||
A symptom checklist for children with cancer: the Therapy-Related Symptom Checklist-Children | Q48629586 | ||
The symptoms of advanced cancer: relationship to age, gender, and performance status in 1,000 patients | Q48722951 | ||
Care-related distress: a nationwide study of parents who lost their child to cancer. | Q50957238 | ||
End of life care in adolescents and young adults with cancer: experience of the adolescent unit of the Institut Gustave Roussy. | Q50995764 | ||
Family caregiver perspective-taking and accuracy in estimating cancer patient symptom experiences. | Q51946210 | ||
Parent and physician perspectives on quality of care at the end of life in children with cancer. | Q53279623 | ||
The memorial symptom assessment scale: modified for use in understanding family caregivers' perceptions of cancer patients' symptom experiences. | Q53381350 | ||
The PedsQL in pediatric cancer: reliability and validity of the Pediatric Quality of Life Inventory Generic Core Scales, Multidimensional Fatigue Scale, and Cancer Module. | Q53442947 | ||
The Memorial Symptom Assessment Scale: an instrument for the evaluation of symptom prevalence, characteristics and distress. | Q53671094 | ||
Symptoms Affecting Children With Malignancies During the Last Month of Life: A Nationwide Follow-up | Q61852808 | ||
Criterion-based validation of the EORTC QLQ-C36 in advanced melanoma: the CIPS questionnaire and proxy raters | Q71417104 | ||
Parents' perceptions of their children's cancer-related symptoms during treatment: a prospective, longitudinal study | Q84635002 | ||
P433 | issue | 22 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 4080-4087 | |
P577 | publication date | 2015-07-28 | |
P1433 | published in | Cancer | Q326041 |
P1476 | title | Symptom profiles in children with advanced cancer: Patient, family caregiver, and oncologist ratings | |
P478 | volume | 121 |
Q90278242 | Mapping child and adolescent self-reported symptom data to clinician-reported adverse event grading to improve pediatric oncology care and research |
Q92255564 | Optimizing symptom control in children and adolescents with cancer |
Q88723608 | Perspectives of children, family caregivers, and health professionals about pediatric oncology symptoms: a systematic review |
Q33439101 | Predictors of acupuncture use among children and adolescents with cancer |
Q40097985 | Providing Pediatric Palliative Care Education Using Problem-Based Learning |
Q47716128 | Symptom Monitoring in Pediatric Oncology Using Patient-Reported Outcomes: Why, How, and Where Next |
Q104491924 | Validation of the caregiver Pediatric Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events measure |
Search more.