Citations (20)
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Louise Sofia Madsen, Jørgen Jeppesen & Charlotte Handberg. (2019) “Understanding my ALS”. Experiences and reflections of persons with amyotrophic lateral sclerosis and relatives on participation in peer group rehabilitation. Disability and Rehabilitation 41:12, pages 1410-1418.
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Tamlyn J. Watermeyer, Richard G. Brown, Katie C. L. Sidle, David J. Oliver, Christopher Allen, Joanna Karlsson, Cathy Ellis, Christopher E. Shaw, Ammar Al-Chalabi & Laura H. Goldstein. (2015) Impact of disease, cognitive and behavioural factors on caregiver outcome in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 16:5-6, pages 316-323.
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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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Jan R. Oyebode, Hayley-Jane Smith & Karen Morrison. (2013) The personal experience of partners of individuals with motor neuron disease. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 14:1, pages 39-43.
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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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Articles from other publishers (15)
Songul DURAN & Yasemin ÇIRAK. (2022) Marital Satisfaction and Sexual Quality of Life of Patients with Amyotrophic Lateral Sclerosis (ALS). Sexuality and Disability 40:4, pages 657-667.
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Mehmet ÖNGER & Tuba AYDIN. (2020) Nörolojik Hastalık ve Evlilik. Sakarya Medical Journal.
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Naoki Hayashi, Naoki Atsuta, Daichi Yokoi, Ryoichi Nakamura, Masahiro Nakatochi, Masahisa Katsuno, Yuishin Izumi, Kazuaki Kanai, Nobutaka Hattori, Akira Taniguchi, Mitsuya Morita, Osamu Kano, Kazumoto Shibuya, Satoshi Kuwabara, Naoki Suzuki, Masashi Aoki, Ikuko Aiba, Kouichi Mizoguchi, Masaya Oda, Ryuji Kaji & Gen Sobue. (2020) Prognosis of amyotrophic lateral sclerosis patients undergoing tracheostomy invasive ventilation therapy in Japan. Journal of Neurology, Neurosurgery & Psychiatry 91:3, pages 285-290.
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Barbara Poletti, Laura Carelli, Federica Solca, Rita Pezzati, Andrea Faini, Nicola Ticozzi, Hiroshi Mitsumoto & Vincenzo Silani. (2019) Sexuality and intimacy in ALS: systematic literature review and future perspectives. Journal of Neurology, Neurosurgery & Psychiatry 90:6, pages 712-719.
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Lucy Holkham & Andy Soundy. (2017) The experience of informal caregivers of patients with motor neurone disease: A thematic synthesis. Palliative and Supportive Care 16:4, pages 487-496.
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Hajime Hino. (2018) Home Care for ALS Patients筋萎縮性側索硬化症患者の在宅ケア. The Japanese Journal of Rehabilitation Medicine 55:7, pages 556-563.
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R. Spataro, P. Volanti, D. Lo Coco & V. La Bella. (2017) Marital status is a prognostic factor in amyotrophic lateral sclerosis. Acta Neurologica Scandinavica 136:6, pages 624-630.
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Mona Shahbazi, Shara Holzberg, Saeyoan Thirunavukkarasu & Gioia Ciani. (2017) Perceptions of sexuality in individuals with Amyotrophic Lateral Sclerosis (ALS) and their treating clinicians. NeuroRehabilitation 41:2, pages 331-342.
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Cathy Gluyas, Susan Mathers, Nicole Hennessy Anderson & Anna Ugalde. (2016) Factors to consider for motor neurone disease carer intervention research: A narrative literature review. Palliative and Supportive Care 15:5, pages 600-608.
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Fumiharu Kimura. (2016) Tracheostomy and invasive mechanical ventilation in amyotrophic lateral sclerosis: decision-making factors and survival analysis. Rinsho Shinkeigaku 56:4, pages 241-247.
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Sabrina Cipolletta & Linda Amicucci. (2015) The family experience of living with a person with amyotrophic lateral sclerosis: A qualitative study. International Journal of Psychology 50:4, pages 288-294.
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Bridget Taylor. (2014) Sexuality, intimacy and motor neurone disease: matters of concern. British Journal of Neuroscience Nursing 10:5, pages 242-251.
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Claire FlahertyAllyson Brothers, Darren Hoffer, Marissa Harrison, Chengwu Yang, Richard S Legro & Zachery Simmons. (2013) VALUES: a national multicenter study demonstrating gender differences in amyotrophic lateral sclerosis with behavioral impairment. Neurodegenerative Disease Management 3:6, pages 515-524.
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Ana Catarina GuedesMaria da Graça Pereira. (2013) Burden, Coping, Physical Symptoms and Psychological Morbidity in Caregivers of Functionally Dependent Family Members. Revista Latino-Americana de Enfermagem 21:4, pages 935-940.
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Samar M Aoun, Brenda Bentley, Laura Funk, Chris Toye, Gunn Grande & Kelli J Stajduhar. (2012) A 10-year literature review of family caregiving for motor neurone disease: Moving from caregiver burden studies to palliative care interventions. Palliative Medicine 27:5, pages 437-446.
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