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Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration Volume 19, 2018 - Issue 7-8
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Research Article

Risk factors for social withdrawal in amyotrophic lateral sclerosis/motor neurone disease

Daniela K. SchlüterCentre for Health informatics, Computing and Statistics (CHICAS), Lancaster Medical School, Lancaster University, Lancaster, UK, Correspondence[email protected]
ORCID Iconhttp://orcid.org/0000-0001-9018-0022View further author information
ORCID Icon,
Alan TennantSwiss Paraplegic Research, Nottwil, Switzerland, View further author information
,
Roger MillsWalton Centre NHS Foundation Trust, Liverpool, UK, View further author information
,
Peter J. DiggleCentre for Health informatics, Computing and Statistics (CHICAS), Lancaster Medical School, Lancaster University, Lancaster, UK, View further author information
&
Carolyn A. YoungWalton Centre NHS Foundation Trust, Liverpool, UK, ;University of Liverpool, Liverpool, UKView further author information
Pages 591-598 | Received 12 May 2018, Accepted 25 Jul 2018, Published online: 06 Nov 2018

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Marion Sommers-Spijkerman, Melinda S. Kavanaugh, Esther Kruitwagen-Van Reenen, Aimée Zwarts-Engelbert, Johanna M. A. Visser-Meily & Anita Beelen. (2023) Stigma experienced by ALS/PMA patients and their caregivers: a mixed-methods study. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 24:3-4, pages 327-338.
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Carolyn A. Young, Roger Mills, Ammar Al-Chalabi, Georgina Burke, Siddharthan Chandran, David J Dick, John Ealing, C. Oliver Hanemann, Timothy Harrower, Christopher J. Mcdermott, Tahir Majeed, Ashwin Pinto, Kevin Talbot, Jannette Walsh, Timothy L. Williams & Alan Tennant. (2020) Measuring quality of life in ALS/MND: validation of the WHOQOL-BREF. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 21:5-6, pages 364-372.
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Articles from other publishers (7)

Yujin Mei, Xue Yang, Changjun Liu, Yuqing Li, Jiaofeng Gui & Lin Zhang. (2023) The impact of psychological resilience on chronic patients’ depression during the dynamic Zero-COVID policy: the mediating role of stigma and the moderating role of sleep quality. BMC Psychology 11:1.
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Eleanor James, Cathy Ellis, Ruth Brassington, Sivakumar Sathasivam & Carolyn A Young. (2022) Treatment for sialorrhea (excessive saliva) in people with motor neuron disease/amyotrophic lateral sclerosis. Cochrane Database of Systematic Reviews 2022:5.
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Yao Wang, Xiaoyu Yang, Qun Han, Min Liu & Chang Zhou. (2022) Prevalence of Sialorrhea Among Amyotrophic Lateral Sclerosis Patients: A Systematic Review and Meta-Analysis. Journal of Pain and Symptom Management 63:4, pages e387-e396.
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Anna L. Beukenhorst, Ella Collins, Katherine M. Burke, Syed Minhajur Rahman, Margaret Clapp, Sai Charan Konanki, Sabrina Paganoni, Timothy M. Miller, James Chan, Jukka‐Pekka Onnela & James D. Berry. (2020) Smartphone data during the COVID ‐19 pandemic can quantify behavioral changes in people with ALS . Muscle & Nerve 63:2, pages 258-262.
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Suzanne Simpson, Sandra Smith, Moira Furlong, Janet Ireland & Clarissa Giebel. (2020) Supporting access to activities to enhance well‐being and reduce social isolation in people living with motor neurone disease. Health & Social Care in the Community 28:6, pages 2282-2289.
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Anne Hogden, Camille Paynter & Karen Hutchinson. (2020) How can we improve patient-centered care of motor neuron disease?. Neurodegenerative Disease Management 10:2, pages 91-97.
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Rhiannon Edge, Roger Mills, Alan Tennant, Peter J. Diggle & Carolyn A. Young. (2019) Do pain, anxiety and depression influence quality of life for people with amyotrophic lateral sclerosis/motor neuron disease? A national study reconciling previous conflicting literature. Journal of Neurology 267:3, pages 607-615.
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