scholarly article | Q13442814 |
P50 | author | Charles S Cleeland | Q88086168 |
P2093 | author name string | Vicente Valero | |
Kai-Ping Liao | |||
Arlene Nazario | |||
Karin Hahn | |||
Araceli Garcia-Gonzalez | |||
Maria L. Jibaja-Weiss | |||
Karen O. Anderson | |||
Tito R. Mendoza | |||
Garrett R. Lynch | |||
Lois M. Ramondetta | |||
Guadalupe R. Palos | |||
P2860 | cites work | Cancer in the elderly population: research issues | Q68702962 |
Families caring for elders in residence: issues in the measurement of burden | Q71276610 | ||
New ACS chief medical officer. Interview by Carrie Printz | Q95811000 | ||
Methodologic issues in collecting data from debilitated patients with cancer near the end of life | Q30760133 | ||
Burden and depression among caregivers of patients with cancer at the end of life | Q34226599 | ||
Guiding research in family care: a new approach to oncology caregiving | Q37059845 | ||
Putting Evidence into Practice: nursing assessment and interventions to reduce family caregiver strain and burden | Q37178596 | ||
Physical and mental health effects of family caregiving | Q37271243 | ||
Cancer and disparities in health: perspectives on health statistics and research questions | Q37272646 | ||
The caregiving experience in a racially diverse sample of cancer family caregivers | Q37407772 | ||
An urban community's preferences for hypothetical outcomes of analgesic pain treatment | Q39773881 | ||
Voices of Mexican American caregivers for family members with cancer: on becoming stronger | Q44417400 | ||
Using navigators to improve care of underserved patients: current practices and approaches | Q46232535 | ||
Caregivers' descriptions of sleep changes and depressive symptoms | Q46624428 | ||
Randomized clinical trial of a family intervention for prostate cancer patients and their spouses | Q47337939 | ||
Poverty, culture, and social injustice: determinants of cancer disparities | Q47346760 | ||
Research with families facing cancer: the challenges of accrual and retention | Q48448160 | ||
When is cancer pain mild, moderate or severe? Grading pain severity by its interference with function | Q48821181 | ||
"Other cancer survivors": the impact on family and caregivers. | Q50765958 | ||
Relatives of the impaired elderly: correlates of feelings of burden. | Q51262952 | ||
The impact of providing symptom management assistance on caregiver reaction: results of a randomized trial. | Q51777884 | ||
Gender differences in caregiver stressors, social resources, and health: an updated meta-analysis. | Q51922547 | ||
The caregiver reaction assessment (CRA) for caregivers to persons with chronic physical and mental impairments | Q52042474 | ||
Assessing symptom distress in cancer patients: the M.D. Anderson Symptom Inventory. | Q53511198 | ||
A SAS Procedure Based on Mixture Models for Estimating Developmental Trajectories | Q58047114 | ||
Correlates of Physical Health of Informal Caregivers: A Meta-Analysis | Q59282078 | ||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | patient | Q181600 |
cost of illness | Q66969671 | ||
health services accessibility | Q67075251 | ||
P304 | page(s) | 1070-1079 | |
P577 | publication date | 2010-10-19 | |
P1433 | published in | Cancer | Q326041 |
P1476 | title | Caregiver symptom burden: the risk of caring for an underserved patient with advanced cancer | |
Caregiver symptom burden: The risk of caring for an underserved patient with advanced cancer | |||
P478 | volume | 117 |
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