Anderson, Lindsey - University of Exeter

个人简介

Lindsey Anderson joined the Medical School in 2007 as a Research Fellow in Child Health. Lindsey co-ordinated the NIHR-HTA funded National Collaborative Study of Lysosomal Storage Disorders (NCS-LSD) longitudinal cohort study which collected clinical and HRQoL data over 3 years, as well as retrospective clinical data, from patients living in the UK with a lysosomal storage disorder. The study aimed to determine natural history of these disorders and estimate effectiveness and cost of therapies. The project was completed in 2011 and has been published as an HTA monograph (Wyatt et al 2012). More recently, Lindsey joined the Cochrane Cardiac Rehabilitation Review Programme, a collaboration between PenTAG and the Cochrane Heart Group (at London School of Hygiene & Tropical Medicine) to update existing Cochrane systematic reviews of rehabilitation interventions for patients with coronary heart disease or heart failure. Lindsey has a background in biochemistry, and prior to joining the Medical School, worked as a Regulatory Affairs and Clinical Trial Manager for a medical devices company. Qualifications PhD, Biochemistry (Cardiff University, 1998) BSc Jt Hons Biochemistry & Microbiology (Aberystwyth University, 1993)

近期论文

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Anderson L, Oldridge N, Thompson DR, Zwisler AD, Rees K, Martin N, Taylor RS (2016). Exercise-Based Cardiac Rehabilitation for Coronary Heart Disease Cochrane Systematic Review and Meta-Analysis. Journal of the American College of Cardiology, 67(1), 1-12. Abstract. Article has an altmetric score of 101 Anderson LJ, Oldridge N, Thompson D, Zwisler AD, Rees K, Martin N, Taylor RS (2016). Exercise-Based Cardiac Rehabilitation for Coronary Heart Disease: Cochrane Systematic Review and Meta-Analysis. JACC, 67, 1-12. Abstract. Anderson LJ, Thompson DR, Oldridge N, Zwisler AD, Rees K, Martin N, Taylor RS (2016). Exercise-based cardiac rehabilitation for coronary heart disease. Cochrane Database of Systematic Reviews(1). Abstract. Full text. Article has an altmetric score of 10 Taylor RS, Anderson LJ (2015). Cochrane corner: cardiac rehabilitation for people with heart disease. Heart, 101(16), 1256-1260. Author URL. Article has an altmetric score of 2 Anderson LJ, Taylor RS (2014). Cardiac rehabilitation for people with heart disease: an overview of Cochrane systematic reviews. Int J Cardiol, 177(2), 348-361. Abstract. Author URL. Full text. Article has an altmetric score of 3 Anderson L, Taylor RS (2014). Cardiac rehabilitation for people with heart disease: an overview of Cochrane systematic reviews. Cochrane Database Syst Rev(12). Abstract. Author URL. Full text. Article has an altmetric score of 53 Anderson LJ, Henley W, Wyatt KM, Nikolaou V, Waldek S, Hughes DA, Lachmann RH, Logan S (2014). Effectiveness of enzyme replacement therapy in adults with late-onset Pompe disease: results from the NCS-LSD cohort study. J Inherit Metab Dis, 37(6), 945-952. Abstract. Author URL. Article has an altmetric score of 2 Anderson LJ, Wyatt KM, Henley W, Nikolaou V, Waldek S, Hughes DA, Pastores GM, Logan S (2014). Long-term effectiveness of enzyme replacement therapy in Fabry disease: results from the NCS-LSD cohort study. J Inherit Metab Dis, 37(6), 969-978. Abstract. Author URL. Anderson LJ, Henley W, Wyatt KM, Nikolaou V, Hughes DA, Waldek S, Logan S (2014). Long-term effectiveness of enzyme replacement therapy in adults with Gaucher disease: results from the NCS-LSD cohort study. J Inherit Metab Dis, 37(6), 953-960. Abstract. Author URL. Article has an altmetric score of 1 Anderson LJ, Henley W, Wyatt KM, Nikolaou V, Waldek S, Hughes DA, Pastores GM, Logan S (2014). Long-term effectiveness of enzyme replacement therapy in children with Gaucher disease: results from the NCS-LSD cohort study. J Inherit Metab Dis, 37(6), 961-968. Abstract. Author URL. Article has an altmetric score of 1 Henley WE, Anderson LJ, Wyatt KM, Nikolaou V, Anderson R, Logan S (2014). The NCS-LSD cohort study: a description of the methods and analyses used to assess the long-term effectiveness of enzyme replacement therapy and substrate reduction therapy in patients with lysosomal storage disorders. J Inherit Metab Dis, 37(6), 939-944. Abstract. Author URL. Wyatt K, Henley W, Anderson L, Anderson R, Nikolaou V, Stein K, Klinger L, Hughes D, Waldek S, Lachmann R, et al (2012). The effectiveness and cost-effectiveness of enzyme and substrate replacement therapies: a longitudinal cohort study of people with lysosomal storage disorders. HEALTH TECHNOLOGY ASSESSMENT, 16(39), V-+. Author URL.