Deep characterization of the anti-drug antibodies developed in Fabry disease patients, a prospective analysis from the French multicenter cohort FFABRY
Published 2018 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Deep characterization of the anti-drug antibodies developed in Fabry disease patients, a prospective analysis from the French multicenter cohort FFABRY
Authors
Keywords
Fabry disease, Anti-drug antibodies, Agalsidase, Lysosomal storage disease, Enzyme replacement therapy, IgG4
Journal
Orphanet Journal of Rare Diseases
Volume 13, Issue 1, Pages -
Publisher
Springer Nature America, Inc
Online
2018-07-31
DOI
10.1186/s13023-018-0877-4
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Characterization of drug-neutralizing antibodies in patients with Fabry disease during infusion
- (2018) Malte Lenders et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Impact of immunosuppressive therapy on therapy-neutralizing antibodies in transplanted patients with Fabry disease
- (2017) M. Lenders et al. JOURNAL OF INTERNAL MEDICINE
- Plasma LysoGb3: A useful biomarker for the diagnosis and treatment of Fabry disease heterozygotes
- (2017) Albina Nowak et al. MOLECULAR GENETICS AND METABOLISM
- Characterization of Classical and Nonclassical Fabry Disease: A Multicenter Study
- (2016) Maarten Arends et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Immune response to enzyme replacement therapies in lysosomal storage diseases and the role of immune tolerance induction
- (2016) Priya S. Kishnani et al. MOLECULAR GENETICS AND METABOLISM
- Genotype: A Crucial but Not Unique Factor Affecting the Clinical Phenotypes in Fabry Disease
- (2016) Xiaoxia Pan et al. PLoS One
- X-chromosome inactivation in female patients with Fabry disease
- (2015) L. Echevarria et al. CLINICAL GENETICS
- Serum-Mediated Inhibition of Enzyme Replacement Therapy in Fabry Disease
- (2015) M. Lenders et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Long-term outcome of enzyme-replacement therapy in advanced Fabry disease: evidence for disease progression towards serious complications
- (2013) F. Weidemann et al. JOURNAL OF INTERNAL MEDICINE
- Investigation of the freely available easy-to-use software ‘EZR’ for medical statistics
- (2012) Y Kanda BONE MARROW TRANSPLANTATION
- Globotriaosylsphingosine Accumulation and Not Alpha-Galactosidase-A Deficiency Causes Endothelial Dysfunction in Fabry Disease
- (2012) Mehdi Namdar et al. PLoS One
- Long-Term Effect of Antibodies against Infused Alpha-Galactosidase A in Fabry Disease on Plasma and Urinary (lyso)Gb3 Reduction and Treatment Outcome
- (2012) Saskia M. Rombach et al. PLoS One
- Anti-α-galactosidase A antibody response to agalsidase beta treatment: Data from the Fabry Registry
- (2011) William R. Wilcox et al. MOLECULAR GENETICS AND METABOLISM
- Globotriaosylsphingosine actions on human glomerular podocytes: implications for Fabry nephropathy
- (2010) M. D. Sanchez-Nino et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- Fabry disease: progression of nephropathy, and prevalence of cardiac and cerebrovascular events before enzyme replacement therapy
- (2009) R. Schiffmann et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now