Citations (16)
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Dvorit Gilad, Hadass Goldblatt & Gabi Zeilig. (2022) End-of-life conversation from both sides of the bed: voices of family and staff. Disability and Rehabilitation 44:12, pages 2774-2783.
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Pär Salander, Mirjam Bergknut & Roger Henriksson. (2014) The creation of hope in patients with lung cancer. Acta Oncologica 53:9, pages 1205-1211.
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Articles from other publishers (14)
Iris Manor-Binyamini & Michal Schreiber-Divon. (2022) Listening to Parents of Children With Cancer—Between Life and its end. Journal of Patient Experience 9, pages 237437352211065.
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Sarah Blaschke, Clare C. O’Callaghan & Penelope Schofield. (2017) Cancer Patients’ Recommendations for Nature-Based Design and Engagement in Oncology Contexts: Qualitative Research. HERD: Health Environments Research & Design Journal 11:2, pages 45-55.
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Sarah Blaschke. (2017) The role of nature in cancer patients' lives: a systematic review and qualitative meta-synthesis. BMC Cancer 17:1.
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Pär Salander. (2017) Patients with cancer react differently – Training in breaking bad news can therefore not be reduced to learning pre-defined behaviours. Patient Education and Counseling 100:10, pages 1955-1956.
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Fereshteh Ahmadi, Jisung Park, Kyung Mee Kim & Nader Ahmadi. (2017) Meaning-Making Coping Among Cancer Patients in Sweden and South Korea: A Comparative Perspective. Journal of Religion and Health 56:5, pages 1794-1811.
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Sarah Blaschke, Clare C. O'Callaghan, Penelope Schofield & Pär Salander. (2017) Cancer patients' experiences with nature: Normalizing dichotomous realities. Social Science & Medicine 172, pages 107-114.
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Fereshteh Ahmadi, Jisung Park, Kyung Mee Kim & Nader Ahmadi. (2016) Exploring Existential Coping Resources: The Perspective of Koreans with Cancer. Journal of Religion and Health 55:6, pages 2053-2068.
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Pär Salander & Sara Lilliehorn. (2016) To carry on as before: A meta-synthesis of qualitative studies in lung cancer. Lung Cancer 99, pages 88-93.
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Joakim Isaksson, Pär Salander, Sara Lilliehorn & Göran Laurell. (2016) Living an everyday life with head and neck cancer 2–2.5 years post-diagnosis – A qualitative prospective study of 56 patients. Social Science & Medicine 154, pages 54-61.
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Pär Salander. (2016) Everyday life as a bridge over troubled water. Psycho-Oncology 25:3, pages 347-348.
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P. Baker, H. Beesley, I. Fletcher, J. Ablett, C. Holcombe & P. Salmon. (2016) ‘Getting back to normal’ or ‘a new type of normal’? A qualitative study of patients' responses to the existential threat of cancer. European Journal of Cancer Care 25:1, pages 180-189.
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Laura Hope-Stone, Stephen L. Brown, Heinrich Heimann, Bertil Damato & Peter Salmon. (2015) How do patients with uveal melanoma experience and manage uncertainty? A qualitative study. Psycho-Oncology 24:11, pages 1485-1491.
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Nicola Mendick, Bridget Young, Christopher Holcombe & Peter Salmon. (2013) The ‘information spectrum’: a qualitative study of how breast cancer surgeons give information and of how their patients experience it. Psycho-Oncology 22:10, pages 2364-2371.
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Paul Baker, Helen Beesley, Robert Dinwoodie, Ian Fletcher, Jan Ablett, Christopher Holcombe & Peter Salmon. (2012) ‘You're putting thoughts into my head’: a qualitative study of the readiness of patients with breast, lung or prostate cancer to address emotional needs through the first 18 months after diagnosis. Psycho-Oncology 22:6, pages 1402-1410.
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