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Kirsty R. Weeks, Rebecca L. Gould, Christopher Mcdermott, Jessica Lynch, Laura H. Goldstein, Christopher D. Graham, Lance McCracken, Marc Serfaty, Robert Howard, Ammar Al-Chalabi, David White, Mike Bradburn, Tracey Young, Cindy Cooper, Dame Pamela J. Shaw & Vanessa Lawrence. (2019) Needs and preferences for psychological interventions of people with motor neuron disease. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 20:7-8, pages 521-531.
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Anne Hogden, David Greenfield, Peter Nugus & Matthew C Kiernan. (2012) What influences patient decision-making in amyotrophic lateral sclerosis multidisciplinary care? A study of patient perspectives. Patient Preference and Adherence 6, pages 829-838.
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Anne Hogden, David Greenfield, Peter Nugus & Matthew C Kiernan. (2012) Engaging in patient decision-making in multidisciplinary care for amyotrophic lateral sclerosis: the views of health professionals. Patient Preference and Adherence 6, pages 691-701.
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Sverre V. Lerum & Jan C. Frich. (2012) Normative assumptions in integrated care: A conceptual discussion. International Journal of Healthcare Management 5:1, pages 32-39.
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Articles from other publishers (4)
Daniel J Paul, Maree Wright, Jonathan M Palmer & Thomas B Russell. (2022) Perioperative management of patients with amyotrophic lateral sclerosis: A narrative review. Anaesthesia and Intensive Care 50:5, pages 345-360.
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Denise Andrea Harris. (2021) Interpreting end-of-life experiences of the person with motor neurone disease. Palliative and Supportive Care 20:2, pages 300-301.
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Sverre Vigeland Lerum, Kari Nyheim Solbrække & Jan C. Frich. (2016) Family caregivers’ accounts of caring for a family member with motor neurone disease in Norway: a qualitative study. BMC Palliative Care 15:1.
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Dorothée Lulé, Benedikt Ehlich, Dirk Lang, Sonja Sorg, Johanna Heimrath, Andrea Kübler, Niels Birbaumer & Albert C. Ludolph. (2013) Quality of life in fatal disease: the flawed judgement of the social environment. Journal of Neurology 260:11, pages 2836-2843.
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