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Research Article

Profile of medical care costs in patients with amyotrophic lateral sclerosis in the Medicare programme and under commercial insurance

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Pages 134-142 | Received 08 Mar 2017, Accepted 23 Jul 2017, Published online: 11 Sep 2017

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Read on this site (4)

Mustafa Çoban, Uğur Bilge, Hale Balseven, Hilmi Uysal & Betül Artut. (2023) The economic evaluation of ALS care: quality and cost. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 24:5-6, pages 502-513.
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James D. Berry, Marie Blanchard, Kerina Bonar, Emma Drane, Molly Murton, Uffe Ploug, Kristen Ricchetti-Masterson, Natasa Savic, Emma Worthington & Terry Heiman-Patterson. (2023) Epidemiology and economic burden of amyotrophic lateral sclerosis in the United States: a literature review. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 24:5-6, pages 436-448.
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Toni Mora, Raúl Domínguez, Abdelilah Assialioui, Andrés Paipa, Ramon Moreno, Xavier Corbella, Antonio Martínez-Yelamos & Mònica Povedano. (2023) Direct health costs of amyotrophic lateral sclerosis in a multidisciplinary ALS unit in Catalonia (Spain). Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 24:1-2, pages 133-138.
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Giuseppe Fiorentino & Antonio M. Esquinas. (2018) Cost-effectiveness associated with amyotrophic lateral sclerosis: some questions and answers pending. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 19:3-4, pages 315-316.
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Eleanor Roberts. (2023) A Review of Oral Fixed-Dose Sodium Phenylbutyrate and Ursodoxicoltaurine in People with Amyotrophic Lateral Sclerosis. EMJ Neurology, pages 2-12.
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Katie Stenson, Lasair O'Callaghan, Jennifer Mellor, Jack Wright, Gregor Gibson, Lucy Earl, Sophie Barlow & Christina Nicole Fournier. (2023) Healthcare resource utilization at different stages of amyotrophic lateral sclerosis: Results from a real-world survey. Journal of the Neurological Sciences 452, pages 120764.
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Heather M. Young, Tina R. Kilaberia, Robin Whitney, Benjamin M. Link, Janice F. Bell, Orly Tonkikh, Jessica Famula & Björn Oskarsson. (2023) Needs of persons living with ALS at home and their family caregivers: A scoping review . Muscle & Nerve 68:3, pages 240-249.
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Eleonora Volpato, Michele Vitacca, Luciana Ptacinsky, Agata Lax, Salvatore D’Ascenzo, Enrica Bertella, Mara Paneroni, Silvia Grilli & Paolo Banfi. (2022) Home-Based Adaptation to Night-Time Non-Invasive Ventilation in Patients with Amyotrophic Lateral Sclerosis: A Randomized Controlled Trial. Journal of Clinical Medicine 11:11, pages 3178.
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K. Achtert & L. Kerkemeyer. (2021) The economic burden of amyotrophic lateral sclerosis: a systematic review. The European Journal of Health Economics 22:8, pages 1151-1166.
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Benjamin Rix Brooks & Jerome E. Kurent. 2021. Public Policy in ALS/MND Care. Public Policy in ALS/MND Care 301 326 .
Nimish J. Thakore, Erik P. Pioro, Belinda L. Udeh, Brittany R. Lapin & Irene L. Katzan. (2020) A Cost-Effectiveness Framework for Amyotrophic Lateral Sclerosis, Applied to Riluzole. Value in Health 23:12, pages 1543-1551.
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Han SongJian-Chao Liu, Zi-Peng CaoWen-Jing LuoJing-Yuan Chen. (2020) Medical cost and healthcare utilization of amyotrophic lateral sclerosis in China. Medicine 99:47, pages e23258.
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Jocelyn Zwicker, Danial Qureshi, Robert TalaricoPierre Bourque, Mary Scott, Nicolas Chin-Yee & Peter Tanuseputro. (2019) Dying of amyotrophic lateral sclerosis. Neurology 93:23.
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Ileana Howard & Abigail Potts. (2019) Interprofessional Care for Neuromuscular Disease. Current Treatment Options in Neurology 21:8.
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Helder Vieira, Nelson Costa, Tomás Sousa, Sara Reis & Luis Coelho. (2019) Voice-Based Classification of Amyotrophic Lateral Sclerosis: Where Are We and Where Are We Going? A Systematic Review. Neurodegenerative Diseases 19:5-6, pages 163-170.
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