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Anna Maksymowicz-Śliwińska, Dorothée Lulé, Krzysztof NieporĘcki, Katarzyna Ciećwierska, Albert C. Ludolph & Magdalena Kuźma-Kozakiewicz. (2023) The quality of life and depression in primary caregivers of patients with amyotrophic lateral sclerosis is affected by patient-related and culture-specific conditions. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 24:3-4, pages 317-326.
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Francesco Pagnini. (2013) Psychological wellbeing and quality of life in amyotrophic lateral sclerosis: A review. International Journal of Psychology 48:3, pages 194-205.
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Mamede de Carvalho, Adriano Chio, Reinhard Dengler, Martin Hecht, Markus Weber & Michael Swash. (2005) Neurophysiological measures in amyotrophic lateral sclerosis: Markers of progression in clinical trials. Amyotrophic Lateral Sclerosis 6:1, pages 17-28.
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Zachary Simmons. (2005) Management Strategies for Patients With Amyotrophic Lateral Sclerosis From Diagnosis Through Death. The Neurologist 11:5, pages 257-270.
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Felicity A. Goodyear-Smith. (2019) Palliative Care Service Needs of Motor Neuron Disease Patients. Journal of Palliative Care 21:2, pages 117-125.
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Marco Orsini, Mariana Mello, Desiree Lisieux, Caroline Pinto Pássaro, Marco Antônio Araújo Leite, Anne Caroline Baldez, Júlio Guilherme Silva, Sara Lúcia Silveira de Menezes, Fábio Henrique Porto, Diones Machado, Victor Hugo Bastos, Marcos RG de Freitas & Acary Bulle Oliveira. (2001) Qualidade de Vida de Cuidadores e Pacientes com Diagnóstico de Esclerose Lateral Amiotrófica. Revista Neurociências 20:2, pages 215-221.
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