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Amyotrophic lateral sclerosis caregiver burden and patients’ quality of life during COVID-19 pandemic

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Pages 146-148 | Received 16 Feb 2021, Accepted 29 Mar 2021, Published online: 16 Apr 2021

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Éilís Conroy, Polly Kennedy, Mark Heverin, Orla Hardiman & Miriam Galvin. (2023) Care, burden and self-described positive aspects of caring in amyotrophic lateral sclerosis: an exploratory, longitudinal, mixed-methods study. BMJ Open 13:1, pages e064254.
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Ling Lian, Minying Zheng, Ruojie He, Jianing Lin, Weineng Chen, Zhong Pei & Xiaoli Yao. (2022) Analysing the influencing factors on caregivers’ burden among amyotrophic lateral sclerosis patients in China: a cross-sectional study based on data mining. BMJ Open 12:9, pages e066402.
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Minoo Sharbafshaaer, Daniela Buonanno, Carla Passaniti, Manuela De Stefano, Sabrina Esposito, Fabrizio Canale, Giulia D’Alvano, Marcello Silvestro, Antonio Russo, Gioacchino Tedeschi, Mattia Siciliano & Francesca Trojsi. (2022) Psychological Support for Family Caregivers of Patients With Amyotrophic Lateral Sclerosis at the Time of the Coronavirus Disease 2019 Pandemic: A Pilot Study Using a Telemedicine Approach. Frontiers in Psychiatry 13.
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Giulia D’Alvano, Daniela Buonanno, Carla Passaniti, Manuela De Stefano, Luigi Lavorgna, Gioacchino Tedeschi, Mattia Siciliano & Francesca Trojsi. (2021) Support Needs and Interventions for Family Caregivers of Patients with Amyotrophic Lateral Sclerosis (ALS): A Narrative Review with Report of Telemedicine Experiences at the Time of COVID-19 Pandemic. Brain Sciences 12:1, pages 49.
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Fabiola De Marchi, Chiara Gallo, Maria Francesca Sarnelli, Ilaria De Marchi, Massimo Saraceno, Roberto Cantello & Letizia Mazzini. (2021) Accelerated Early Progression of Amyotrophic Lateral Sclerosis over the COVID-19 Pandemic. Brain Sciences 11:10, pages 1291.
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