<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Germain DP</submitter><funding>National Institute for Health Research (NIHR)</funding><pagination>100454</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6365982</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>19</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Enzyme replacement therapy (ERT) with recombinant human α-galactosidase has been available for the treatment of Fabry disease since 2001 in Europe and 2003 in the USA. Treatment outcomes with ERT are dependent on baseline patient characteristics, and published data are derived from heterogeneous study populations.&lt;h4>Methods&lt;/h4>We conducted a comprehensive systematic literature review of all original articles on ERT in the treatment of Fabry disease published up until January 2017. This article presents the findings in adult male patients.&lt;h4>Results&lt;/h4>Clinical evidence for the efficacy of ERT in adult male patients was available from 166 publications including 36 clinical trial publications. ERT significantly decreases globotriaosylceramide levels in plasma, urine, a</pubmed_abstract><journal>Molecular genetics and metabolism reports</journal><pubmed_title>The effect of enzyme replacement therapy on clinical outcomes in male patients with Fabry disease: A systematic literature review by a European panel of experts.</pubmed_title><pmcid>PMC6365982</pmcid><funding_grant_id>NIHR200158</funding_grant_id><pubmed_authors>Spada M</pubmed_authors><pubmed_authors>Oliveira JP</pubmed_authors><pubmed_authors>Elliott PM</pubmed_authors><pubmed_authors>Nowak A</pubmed_authors><pubmed_authors>Namdar M</pubmed_authors><pubmed_authors>Wanner C</pubmed_authors><pubmed_authors>Falissard B</pubmed_authors><pubmed_authors>Viana-Baptista M</pubmed_authors><pubmed_authors>Linhart A</pubmed_authors><pubmed_authors>Germain DP</pubmed_authors><pubmed_authors>Fomin VV</pubmed_authors><pubmed_authors>Jovanovic A</pubmed_authors><pubmed_authors>Hilz MJ</pubmed_authors><pubmed_authors>Mignani R</pubmed_authors><pubmed_authors>Pieroni M</pubmed_authors><pubmed_authors>Kantola I</pubmed_authors></additional><is_claimable>false</is_claimable><name>The effect of enzyme replacement therapy on clinical outcomes in male patients with Fabry disease: A systematic literature review by a European panel of experts.</name><description>&lt;h4>Background&lt;/h4>Enzyme replacement therapy (ERT) with recombinant human α-galactosidase has been available for the treatment of Fabry disease since 2001 in Europe and 2003 in the USA. Treatment outcomes with ERT are dependent on baseline patient characteristics, and published data are derived from heterogeneous study populations.&lt;h4>Methods&lt;/h4>We conducted a comprehensive systematic literature review of all original articles on ERT in the treatment of Fabry disease published up until January 2017. This article presents the findings in adult male patients.&lt;h4>Results&lt;/h4>Clinical evidence for the efficacy of ERT in adult male patients was available from 166 publications including 36 clinical trial publications. ERT significantly decreases globotriaosylceramide levels in plasma, urine, a</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jun</publication><modification>2026-05-05T01:28:38.699Z</modification><creation>2019-03-26T22:55:33Z</creation></dates><accession>S-EPMC6365982</accession><cross_references><pubmed>30775256</pubmed><doi>10.1016/j.ymgmr.2019.100454</doi></cross_references></HashMap>