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Expert Review of Pharmacoeconomics & Outcomes Research Volume 7, 2007 - Issue 4
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Review

Patient-reported outcomes measurements in epilepsy

Megan Stafford United BioSource Corporation, 20 Bloomsbury Square, London, WC1A 2NS, UK. [email protected]
,
Sonia Gavriel United BioSource Corporation, London, UK
&
Andrew Lloyd United BioSource Corporation, London, UK
Pages 373-384 | Published online: 09 Jan 2014

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Read on this site (2)

Lidia MVR Moura, Eli L Schwamm, Valdery Moura Junior, Michael P Seitz, Daniel B Hoch, John Hsu & Lee H Schwamm. (2016) Patient-reported financial barriers to adherence to treatment in neurology. ClinicoEconomics and Outcomes Research 8, pages 685-694.
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Ann Jacoby, Gus A Baker, Joanne Crossley & Steven Schachter. (2013) Tools for assessing quality of life in epilepsy patients. Expert Review of Neurotherapeutics 13:12, pages 1355-1369.
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Articles from other publishers (6)

Tolulope T. Sajobi, Colin B. Josephson, Richard Sawatzky, Meng Wang, Oluwaseyi Lawal, Scott B. Patten, Lisa M. Lix & Samuel Wiebe. (2021) Quality of Life in Epilepsy: Same questions, but different meaning to different people. Epilepsia 62:9, pages 2094-2102.
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Felipe J.S. Jones, Farrah L. Ezzeddine, Susan T. Herman, Jeffrey Buchhalter, Brandy Fureman & Lidia M.V.R. Moura. (2020) A feasibility assessment of functioning and quality-of-life patient-reported outcome measures in adult epilepsy clinics: A systematic review. Epilepsy & Behavior 102, pages 106704.
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M. Mevaag, O. Henning, A. Baftiu, A. G. Granas, S. I. Johannessen, K. O. Nakken & C. Johannessen Landmark. (2017) Discrepancies between physicians' prescriptions and patients' use of antiepileptic drugs. Acta Neurologica Scandinavica 135:1, pages 80-87.
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Lidia M.V.R. Moura, Thiago S. Carneiro, Emily L. Thorn, Michael P. Seitz, John Hsu, Andrew J. Cole, Barbara G. Vickrey & Daniel B. Hoch. (2016) Patient perceptions of physician-documented quality care in epilepsy. Epilepsy & Behavior 62, pages 90-96.
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Barbara Blachut, Christian Hoppe, Rainer Surges, Jutta Stahl, Christian E. Elger & Christoph Helmstaedter. (2015) Counting seizures: The primary outcome measure in epileptology from the patients’ perspective. Seizure 29, pages 97-103.
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Robert S. Fisher, David E. Blum, Bree DiVentura, Jennifer Vannest, John D. Hixson, Robert Moss, Susan T. Herman, Brandy E. Fureman & Jacqueline A. French. (2012) Seizure diaries for clinical research and practice: Limitations and future prospects. Epilepsy & Behavior 24:3, pages 304-310.
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