Citations (28)
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Mariana P. Branco, Elmar G. M. Pels, Femke Nijboer, Nick F. Ramsey & Mariska J. Vansteensel. (2023) Brain-Computer interfaces for communication: preferences of individuals with locked-in syndrome, caregivers and researchers. Disability and Rehabilitation: Assistive Technology 18:6, pages 963-973.
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C. Paynter, S. Mathers, H. Gregory, A. P. Vogel & M. Cruice. (2022) How people living with motor neurone disease and their carers experience healthcare decision making: a qualitative exploration. Disability and Rehabilitation 44:13, pages 3095-3103.
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Anne Hogden, Geraldine Foley, Robert D Henderson, Natalie James & Samar M Aoun. (2017) Amyotrophic lateral sclerosis: improving care with a multidisciplinary approach. Journal of Multidisciplinary Healthcare 10, pages 205-215.
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Silvana Castillo-Parra, Sandra Oyarzo Torres, Mónica Espinoza Barrios, Ana María Rojas-Serey, Juan Diego Maya, Valeria Sabaj Diez, Verónica Aliaga Castillo, Manuel Castillo Niño, Luis Romero Romero, Jennifer Foster & Gustavo Hawes Barrios. (2017) The implementation of multiple interprofessional integrated modules by health sciences faculty in Chile. Journal of Interprofessional Care 31:6, pages 777-780.
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David Oliver, Aleksandar Radunovic, Alexander Allen & Christopher McDermott. (2017) The development of the UK National Institute of Health and Care Excellence evidence-based clinical guidelines on motor neurone disease. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 18:5-6, pages 313-323.
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Anne Hogden, David Greenfield, Peter Nugus & Matthew C Kiernan. (2013) What are the roles of carers in decision-making for amyotrophic lateral sclerosis multidisciplinary care?. Patient Preference and Adherence 7, pages 171-181.
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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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Articles from other publishers (21)
Shelagh K. Genuis, Westerly Luth, Tania Bubela & Wendy S. Johnston. (2022) Covid-19 threat and coping: application of protection motivation theory to the pandemic experiences of people affected by amyotrophic lateral sclerosis. BMC Neurology 22:1.
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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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Anke Erdmann, Celia Spoden, Irene Hirschberg & Gerald Neitzke. (2022) Talking about the end of life: communication patterns in amyotrophic lateral sclerosis – a scoping review. Palliative Care and Social Practice 16, pages 263235242210836.
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Mitsuko Ushikubo, Emiko Nashiki, Tadahiro Ohtani & Hiromi Kawabata. (2021) Practical Measures for Dealing With the Struggles of Nurses Caring for People With Amyotrophic Lateral Sclerosis Comorbid With Cognitive Impairment in Japan. Frontiers in Psychology 12.
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Shelagh K. Genuis, Westerly Luth, Sandra Campbell, Tania Bubela & Wendy S. Johnston. (2021) Communication About End of Life for Patients Living With Amyotrophic Lateral Sclerosis: A Scoping Review of the Empirical Evidence. Frontiers in Neurology 12.
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Xiaoxu Zeng, Bin Li & Yang Zou. (2021) The relationship between non-alcoholic fatty liver disease and hypothyroidism. Medicine 100:17, pages e25738.
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Julie Labra, Anne Hogden, Emma Power, Natalie James & Victoria M Flood. (2020) Gastrostomy uptake in motor neurone disease: a mixed-methods study of patients’ decision making. BMJ Open 10:2, pages e034751.
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Christoph Heesen, Anne Rahn & Insa Schiffmann. 2020. Diagnostik und Therapie neurologischer Erkrankungen. Diagnostik und Therapie neurologischer Erkrankungen
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Jashelle Caga, Sharpley Hsieh, Patricia Lillo, Kaitlin Dudley & Eneida Mioshi. (2019) The Impact of Cognitive and Behavioral Symptoms on ALS Patients and Their Caregivers. Frontiers in Neurology 10.
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Anne Hogden, Samar M. Aoun & Peter L. Silbert. (2018) Palliative Care in Neurology: Integrating a Palliative Approach to Amyotrophic Lateral Sclerosis Care. EMJ Neurology, pages 68-76.
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Liselott Årestedt, Carina Persson, Margareta Rämgård & Eva Benzein. (2017) Experiences of encounters with healthcare professionals through the lenses of families living with chronic illness. Journal of Clinical Nursing 27:3-4, pages 836-847.
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Michiko Nakai, Yugo Narita & Hidekazu Tomimoto. (2017) An Investigation of Perspectives of Respite Admission Among People Living With Amyotrophic Lateral Sclerosis and the Hospitals That Support Them. Journal of Primary Care & Community Health 8:3, pages 163-168.
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Sverre Vigeland Lerum, Kari Nyheim Solbraekke & Jan C. Frich. (2017) Healthcare professionals’ accounts of challenges in managing motor neurone disease in primary healthcare: a qualitative study. Health & Social Care in the Community 25:4, pages 1355-1363.
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Helena E. A. Aho-Özhan, Sarah Böhm, Jürgen Keller, Johannes Dorst, Ingo Uttner, Albert C. Ludolph & Dorothée Lulé. (2017) Experience matters: neurologists’ perspectives on ALS patients’ well-being. Journal of Neurology 264:4, pages 639-646.
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Naomi H. Martin, Vanessa Lawrence, Joanna Murray, Anna Janssen, Irene Higginson, Rebecca Lyall, Rachel Burman, P. Nigel Leigh, Ammar Al-Chalabi & Laura H. Goldstein. (2015) Decision Making About Gastrostomy and Noninvasive Ventilation in Amyotrophic Lateral Sclerosis. Qualitative Health Research 26:10, pages 1366-1381.
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Samar M. Aoun, Lauren J. Breen, Robert Edis, Robert D. Henderson, David Oliver, Rodney Harris, Denise Howting, Margaret O'Connor & Carol Birks. (2016) Breaking the news of a diagnosis of motor neurone disease: A national survey of neurologists' perspectives. Journal of the Neurological Sciences 367, pages 368-374.
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Shahla Siddiqui. (2016) Dying within dying: Ethical dilemmas of treating terminally ill patients with acute life-threatening illnesses. Indian Journal of Critical Care Medicine 20:5, pages 308-309.
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Anne Hogden, David Greenfield, Jashelle Caga & Xiongcai Cai. (2016) Development of patient decision support tools for motor neuron disease using stakeholder consultation: a study protocol. BMJ Open 6:4, pages e010532.
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Anne Hogden, David Greenfield, Peter Nugus & Matthew C Kiernan. (2015) Development of a model to guide decision making in amyotrophic lateral sclerosis multidisciplinary care. Health Expectations 18:5, pages 1769-1782.
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Anne Hogden. (2014) Optimizing patient autonomy in amyotrophic lateral sclerosis: inclusive decision-making in multidisciplinary care. Neurodegenerative Disease Management 4:1, pages 1-3.
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