| review article | Q7318358 |
| scholarly article | Q13442814 |
| systematic review | Q1504425 |
| P6179 | Dimensions Publication ID | 1000179553 |
| P356 | DOI | 10.1007/S11136-016-1239-0 |
| P8608 | Fatcat ID | release_2vw3lsazh5csdn3zjs5w2q2q54 |
| P932 | PMC publication ID | 4945691 |
| P698 | PubMed publication ID | 26872911 |
| P50 | author | Lesley Fallowfield | Q23772391 |
| P2093 | author name string | Valerie Jenkins | |
| Lucy Matthews | |||
| Valerie Shilling | |||
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| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 8 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | psychometrics | Q506132 |
| caregiver | Q553079 | ||
| neoplasm | Q1216998 | ||
| patient reported outcome measures | Q70453213 | ||
| P5008 | on focus list of Wikimedia project | ScienceSource | Q55439927 |
| P304 | page(s) | 1859-76 | |
| P577 | publication date | 2016-08-01 | |
| P1433 | published in | Quality of Life Research | Q15749950 |
| P1476 | title | Patient-reported outcome measures for cancer caregivers: a systematic review | |
| P478 | volume | 25 |
| Q91606769 | A comparison of psychometric properties of two common measures of caregiving burden: the family burden interview schedule (FBIS-24) and the Zarit caregiver burden interview (ZBI-22) |
| Q47565322 | Caregiver quality of life in advanced cancer: Qualitative results from a trial of early palliative care |
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| Q60198826 | Development and validation of the patient roles and responsibilities scale in cancer patients |
| Q47609321 | Family Caregiver Communication Tool: a new measure for tailoring communication with cancer caregivers |
| Q47683879 | Family Caregivers to Adults with Cancer: The Consequences of Caring |
| Q92754752 | Identification and evaluation of observational measures for the assessment and/or monitoring of level of consciousness in adult palliative care patients: A systematic review for I-CAN-CARE |
| Q39451782 | Life impact of caregiving for severe childhood epilepsy: Results of expert panels and caregiver focus groups |
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| Q41686442 | Psychometric evaluation of the Shona version of the Multidimensional Scale of Perceived Social Support Scale (MSPSS-Shona) in adult informal caregivers of patients with cancer in Harare, Zimbabwe |
| Q37629609 | Silent strain of caregiving: exploring the best predictors of distress in family carers of geriatric patients |
| Q38692222 | The humanistic and economic burden of Dravet syndrome on caregivers and families: Implications for future research |
| Q38655483 | The pervasive nature of uncertainty-a qualitative study of patients with advanced cancer and their informal caregivers |
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