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2.Risk factors for severe clinical events in male and female patients with Fabry disease treated with agalsidase beta enzyme replacement therapy: Data from the Fabry Registry
作者:Robert J. Hopkina ; b ; rob.hopkin@cchmc.org" class="auth_mail" title="E-mail the corresponding author ; Gustavo Cabrerac ; gustavo.h.cabrera@hotmail.com" class="auth_mail" title="E-mail the corresponding author ; Joel Charrowd ; jcharrow@northwestern.edu" class="auth_mail" title="E-mail the corresponding author ; Roberta Lemaye ; Roberta.Lemay@genzyme.com" class="auth_mail" title="E-mail the corresponding author ; Ana Maria Martinsf ; martins.anamaria@uol.com.br" class="auth_mail" title="E-mail the corresponding author ; Michael Mauerg ; mauer002@umn.edu" class="auth_mail" title="E-mail the corresponding author ; Alberto Ortizh ; AOrtiz@fjd.es" class="auth_mail" title="E-mail the corresponding author ; Manesh R. Pateli ; patel017@mc.duke.edu" class="auth_mail" title="E-mail the corresponding author ; Katherine Simsj ; Sims@Helix.MGH.Harvard.edu" class="auth_mail" title="E-mail the corresponding author ; Stephen Waldekk ; stephen.waldek@sunderland.ac.uk" class="auth_mail" title="E-mail the corresponding author ; David G. Warnockl ; dwarnock@uab.edu" class="auth_mail" title="E-mail the corresponding author ; William R. Wilcoxm ; william.wilcox@emory.edu" class="auth_mail" title="E-mail the corresponding author
刊名:Molecular Genetics and Metabolism
出版年:2016
3.The management and treatment of children with Fabry disease: A United States-based perspective
刊名:Molecular Genetics and Metabolism
出版年:2016
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