| scholarly article | Q13442814 |
| P356 | DOI | 10.1111/J.1471-6712.2008.00613.X |
| P698 | PubMed publication ID | 19645802 |
| P50 | author | Cynthia Peden-McAlpine | Q103444666 |
| P2093 | author name string | Charles E Gessert | |
| Barbara A Elliott | |||
| P2860 | cites work | Narrative based medicine: narrative in medical ethics | Q33793468 |
| The concept of theme as used in qualitative nursing research | Q33914966 | ||
| Values and voices in teaching gerontology and geriatrics: case studies as stories | Q34662579 | ||
| Applying thematic analysis theory to practice: a researcher's experience | Q36259261 | ||
| Rigor or rigor mortis: the problem of rigor in qualitative research revisited | Q40815893 | ||
| The accuracy of substituted judgments in patients with terminal diagnoses. | Q52229888 | ||
| All in the Family: Extended Autonomy and Expectations in Surrogate Health Care Decision-Making1 | Q56144080 | ||
| P433 | issue | 2 | |
| P921 | main subject | dementia | Q83030 |
| decision making | Q1331926 | ||
| P304 | page(s) | 251-258 | |
| P577 | publication date | 2009-06-01 | |
| P1433 | published in | Scandinavian Journal of Caring Sciences | Q15756988 |
| P1476 | title | Family decision-making in advanced dementia: narrative and ethics | |
| P478 | volume | 23 |
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| Q51762615 | Care Values in Dementia: Patterns of Perception and Incongruence Among Family Care Dyads. |
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| Q39701531 | Couple meaning-making and dementia: challenges to the deficit model |
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