b6c0ea3b71424f89f84fc45cc0ed4578 pmc_29159077.pdf ce37c4f1498a7cb2bb35d5ddb4d06a17c104beb2 pmc_29159077.pdf c37af12c103121b68acbe41ec0ff93fdbc95172bda393d83322fe70085ee2217 pmc_29159077.pdf Title: Long-term outcomes with agalsidase alfa enzyme replacement therapy_ Analysis using deconstructed composite events Subject: Molecular Genetics and Metabolism Reports, 14 (2018) 31-35. doi:10.1016/j.ymgmr.2017.10.008 Keywords: Fabry disease; Enzyme replacement therapy; Agalsidase alfa; Long-term effectiveness Author: Michael Beck Creator: Elsevier CreationDate: Fri Jan 5 11:37:07 2018 CET ModDate: Fri Jan 5 11:37:07 2018 CET Tagged: no UserProperties: no Suspects: no Form: AcroForm JavaScript: no Pages: 5 Encrypted: no Page size: 595.276 x 793.701 pts Page rot: 0 File size: 252286 bytes Optimized: yes PDF version: 1.7 name type encoding emb sub uni object ID ------------------------------------ ----------------- ---------------- --- --- --- --------- VXDGDH+CharisSIL CID Type 0C Identity-H yes yes yes 294 0 PDMALE+AdvOT596495f2 Type 1C WinAnsi yes yes no 267 0 PDMAME+AdvOT0de51fd2 Type 1C WinAnsi yes yes no 268 0 PDMANF+AdvOT8608a8d1+20 Type 1C Custom yes yes yes 269 0 PDMANG+AdvOT7fb33346.I Type 1C WinAnsi yes yes no 275 0 PDMAOH+AdvOT7fb33346.I+20 Type 1C WinAnsi yes yes no 276 0 PDMAOI+AdvOT596495f2+fb Type 1C Custom yes yes yes 277 0 PDMAOJ+AdvOT1efcda3b.B Type 1C WinAnsi yes yes no 283 0 PDMAOK+AdvOT596495f2+03 Type 1C Custom yes yes yes 284 0 PDMAOL+AdvOT596495f2+20 Type 1C WinAnsi yes yes no 285 0 PDMAOM+AdvOT596495f2+22 Type 1C Custom yes yes yes 290 0 OKRQJV+CharisSIL-Italic CID Type 0C Identity-H yes yes yes 116 0 PDMBDL+Helvetica Type 1C WinAnsi yes yes no 113 0 PDMBDM+Helvetica-Oblique Type 1C WinAnsi yes yes no 110 0 PDMBEM+Helvetica-Bold Type 1C WinAnsi yes yes no 109 0 PDMBFN+AdvOT1efcda3b.B+fb Type 1C Custom yes yes yes 125 0 Jhove (Rel. 1.6, 2011-01-04) Date: 2019-02-14 17:44:54 CET RepresentationInformation: pmc_29159077.pdf ReportingModule: PDF-hul, Rel. 1.8 (2009-05-22) LastModified: 2018-02-08 07:41:28 CET Size: 252286 Format: PDF Version: 1.7 Status: Well-Formed and valid SignatureMatches: PDF-hul MIMEtype: application/pdf Profile: Linearized PDF PDFMetadata: Objects: 347 FreeObjects: 1 IncrementalUpdates: 1 DocumentCatalog: PageLayout: SinglePage PageMode: UseOutlines Outlines: Item: Title: Long-term outcomes with agalsidase alfa enzyme replacement therapy: Analysis using deconstructed composite events Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@7c53a9eb Children: Item: Title: Introduction Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@ed17bee Item: Title: Materials and methods Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@2a33fae0 Item: Title: Results Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@707f7052 Item: Title: Discussion Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@11028347 Item: Title: Role of the funding source Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@14899482 Item: Title: Contributions Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@21588809 Item: Title: Conflict of interest Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@2aae9190 Item: Title: Funding Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@2f333739 Item: Title: Appendix A Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@77468bd9 Item: Title: References Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@12bb4df8 Info: Title: Long-term outcomes with agalsidase alfa enzyme replacement therapy_ Analysis using deconstructed composite events Author: Michael Beck Subject: Molecular Genetics and Metabolism Reports, 14 (2018) 31-35. doi:10.1016/j.ymgmr.2017.10.008 Keywords: Fabry disease; 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West Roberto Giugliani Fabry disease Enzyme replacement therapy Agalsidase alfa Long-term effectiveness Elsevier Molecular Genetics and Metabolism Reports, 14 (2018) 31-35. doi:10.1016/j.ymgmr.2017.10.008 journal Molecular Genetics and Metabolism Reports © 2017 The Authors. 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