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The Clinical Guide to Supportive and Palliative Care for HIV/AIDS

The Clinical Guide to Supportive and Palliative Care for HIV/AIDS

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A <strong>Clinical</strong> <strong>Guide</strong> <strong>to</strong> <strong>Supportive</strong> <strong>and</strong> <strong>Palliative</strong> <strong>Care</strong> <strong>for</strong> <strong>HIV</strong>/<strong>AIDS</strong> • Chapter 3: Assessment of Physical Symp<strong>to</strong>ms21. Clipp EC, George LK. Patients with cancer <strong>and</strong> their spouse caregivers. Perceptions of the illnessexperience. Cancer 69:1074-9, 1992.22. Higginson I, Priest P, McCarthy M. Are bereaved family members a valid proxy <strong>for</strong> a patient’s assessment ofdying? 26 picas Soc Sci Med 38:553-7, 1994.23. Slevin ML, Plant H, Lynch D, et al. Who should measure quality of life, the doc<strong>to</strong>r or the patient. Br JCancer 57:109, 1988.24. Kahn SB, Houts PS, Harding SP. Quality of life <strong>and</strong> patients with cancer: a comparative study of patientversus physician perceptions <strong>and</strong> its implications <strong>for</strong> cancer education. 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