Long-term effectiveness of agalsidase alfa enzyme replacement in Fabry disease: A Fabry Outcome Survey analysis

Molecular Genetics and Metabolism Reports - Tập 3 - Trang 21-27 - 2015
Michael Beck1, Derralynn Hughes2, Christoph Kampmann1, Sylvain Larroque3, Atul Mehta2, Guillem Pintos-Morell4, Uma Ramaswami2, Michael West5, Anna Wijatyk6, Roberto Giugliani7
1University Medical Center, University of Mainz, Department of Paediatrics, Mainz, Germany
2Royal Free London NHS Foundation Trust, University College of London, UK
3Shire, Zug, Switzerland
4Department of Pediatrics, University Hospital “Germans Trias i Pujol," Badalona, Universitat Autònoma de Barcelona, Spain
5Department of Medicine, Dalhousie University, Halifax, Nova Scotia Canada
6Shire, Lexington, MA, USA
7Medical Genetics Service HCPA/Dep Genet UFRGS and INAGEMP, Porto Alegre, Brazil

Tài liệu tham khảo

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