The Multiple Sclerosis Surveillance Registry: A Novel Interactive Database Within the Veterans Health Administration.
暂无分享,去创建一个
J. Haselkorn | M. Wallin | R. Whitham | H. Maloni | W. Culpepper | J. Duckart | Shan Jin
[1] A. Salter,et al. Data harmonization for collaborative research among MS registries: A case study in employment , 2020, Multiple sclerosis.
[2] K. Myhr,et al. Validation of the multiple sclerosis diagnosis in the Norwegian Patient Registry , 2019, Brain and behavior.
[3] H. Butzkueven,et al. The MSBase registry: Informing clinical practice , 2019, Multiple sclerosis.
[4] F. Piehl,et al. Validation of the Swedish Multiple Sclerosis Register , 2019, Epidemiology.
[5] L. Iezzoni,et al. Use and cost of disease-modifying therapies by Sonya Slifka Study participants: has anything really changed since 2000 and 2009? , 2019, Multiple sclerosis journal - experimental, translational and clinical.
[6] M. Ramanathan,et al. Fatigue at enrollment predicts EDSS worsening in the New York State Multiple Sclerosis Consortium , 2018, Multiple sclerosis.
[7] Luiz C. Mostaço-Guidolin,et al. Registry Cohort Study to Determine Risk for Multiple Sclerosis after Vaccination for Pandemic Influenza A(H1N1) with Arepanrix, Manitoba, Canada , 2018, Emerging infectious diseases.
[8] Alan J Thompson,et al. Landscape of MS patient cohorts and registries: Recommendations for maximizing impact , 2017, Multiple sclerosis.
[9] G. McDonnell. Quality improvement in neurology: Multiple sclerosis quality measures: Executive summary , 2016, Neurology.
[10] Christina Wolfson,et al. High incidence and increasing prevalence of multiple sclerosis in British Columbia, Canada: findings from over two decades (1991–2010) , 2015, Journal of Neurology.
[11] B. Laursen,et al. Registers of multiple sclerosis in Denmark , 2015, Acta neurologica Scandinavica.
[12] Deborah M. Miller,et al. Risk tolerance to MS therapies: Survey results from the NARCOMS registry. , 2015, Multiple sclerosis and related disorders.
[13] L. Magder,et al. VHA Multiple Sclerosis Surveillance Registry and its similarities to other contemporary multiple sclerosis cohorts. , 2015, Journal of rehabilitation research and development.
[14] Marram P. Olson,et al. Precision medicine in chronic disease management: The multiple sclerosis BioScreen , 2014, Annals of neurology.
[15] A. Traboulsee,et al. How useful are MS registries? , 2014, Multiple sclerosis.
[16] P. Flachenecker. Multiple Sclerosis Databases: Present and Future , 2014, European Neurology.
[17] T. Friede,et al. Multiple sclerosis registries in Europe – results of a systematic survey , 2014, Multiple sclerosis.
[18] B. Yawn,et al. History of the Rochester Epidemiology Project: half a century of medical records linkage in a US population. , 2012, Mayo Clinic proceedings.
[19] J. Haselkorn,et al. The Gulf War era multiple sclerosis cohort: age and incidence rates by race, sex and service. , 2012, Brain : a journal of neurology.
[20] G. Cutter,et al. Trend for decreasing Multiple Sclerosis Severity Scores (MSSS) with increasing calendar year of enrollment into the New York State Multiple Sclerosis Consortium , 2011, Multiple sclerosis.
[21] George C. Ebers,et al. The natural history of multiple sclerosis, a geographically based study 10: relapses and long-term disability , 2010, Brain : a journal of neurology.
[22] D. Hoaglin,et al. The Sonya Slifka Longitudinal Multiple Sclerosis Study: methods and sample characteristics , 2006, Multiple sclerosis.