Anti-α-galactosidase A antibody response to agalsidase beta treatment: data from the Fabry Registry (Q34121326)

31 July 2017

Anti-α-galactosidase A antibody response to agalsidase beta treatment: data from the Fabry Registry (English)

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31 July 2017

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Dominique P Germain

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David G Warnock

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David G Warnock

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Ulla Feldt-Rasmussen

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William R Wilcox

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Gabor E Linthorst

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Stephen Waldek

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Susan M Richards

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Dana Beitner-Johnson

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Marta Cizmarik

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J Alexander Cole

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Wytske Kingma

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14 December 2011

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Molecular Genetics and Metabolism

31 July 2017

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443-449

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2011.12.006

31 July 2017

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Natural history of Fabry renal disease: influence of alpha-galactosidase A activity and genetic mutations on clinical course

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2011.12.006

End-stage renal disease in patients with Fabry disease: natural history data from the Fabry Registry

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2011.12.006

Fabry disease: progression of nephropathy, and prevalence of cardiac and cerebrovascular events before enzyme replacement therapy

7 January 2021

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Stroke in Fabry disease frequently occurs before diagnosis and in the absence of other clinical events: natural history data from the Fabry Registry

7 January 2021

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Prognostic indicators of renal disease progression in adults with Fabry disease: natural history data from the Fabry Registry

7 January 2021

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Females with Fabry disease frequently have major organ involvement: lessons from the Fabry Registry.

7 January 2021

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Safety and efficacy of recombinant human alpha-galactosidase A replacement therapy in Fabry's disease

7 January 2021

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Sustained, long-term renal stabilization after 54 months of agalsidase beta therapy in patients with Fabry disease

7 January 2021

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Agalsidase-beta therapy for advanced Fabry disease: a randomized trial

7 January 2021

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Human immune response to recombinant human proteins

7 January 2021

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Neutralizing antibodies to therapeutic enzymes: considerations for testing, prevention and treatment

7 January 2021

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A retrospective analysis of the potential impact of IgG antibodies to agalsidase beta on efficacy during enzyme replacement therapy for Fabry disease

7 January 2021

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Treatment of Fabry disease with different dosing regimens of agalsidase: effects on antibody formation and GL-3.

7 January 2021

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Liquid chromatography-tandem mass spectrometry quantification of globotriaosylceramide in plasma for long-term monitoring of Fabry patients treated with enzyme replacement therapy

7 January 2021

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Evaluation of a low dose, after a standard therapeutic dose, of agalsidase beta during enzyme replacement therapy in patients with Fabry disease

7 January 2021

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Influence of antibody formation on reduction of globotriaosylceramide (GL-3) in urine from Fabry patients during agalsidase beta therapy

7 January 2021

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Biomarkers in the diagnosis of lysosomal storage disorders: proteins, lipids, and inhibodies

7 January 2021

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Reduction of elevated plasma globotriaosylsphingosine in patients with classic Fabry disease following enzyme replacement therapy

7 January 2021

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Enzyme replacement therapy in Fabry disease: a randomized controlled trial

7 January 2021

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Enzyme therapy for Fabry disease: neutralizing antibodies toward agalsidase alpha and beta

7 January 2021

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10.1016/J.YMGME.2011.12.006

7 January 2021

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31 July 2017

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