4.5 Article

Deep characterization of the anti-drug antibodies developed in Fabry disease patients, a prospective analysis from the French multicenter cohort FFABRY

Related references

Note: Only part of the references are listed.
Article Allergy

Characterization of drug-neutralizing antibodies in patients with Fabry disease during infusion

Malte Lenders et al.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2018)

Article Urology & Nephrology

Characterization of Classical and Nonclassical Fabry Disease: A Multicenter Study

Maarten Arends et al.

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2017)

Article Medicine, General & Internal

Impact of immunosuppressive therapy on therapy-neutralizing antibodies in transplanted patients with Fabry disease

M. Lenders et al.

JOURNAL OF INTERNAL MEDICINE (2017)

Article Endocrinology & Metabolism

Plasma LysoGb3: A useful biomarker for the diagnosis and treatment of Fabry disease heterozygotes

Albina Nowak et al.

MOLECULAR GENETICS AND METABOLISM (2017)

Article Genetics & Heredity

X-chromosome inactivation in female patients with Fabry disease

L. Echevarria et al.

CLINICAL GENETICS (2016)

Article Urology & Nephrology

Serum-Mediated Inhibition of Enzyme Replacement Therapy in Fabry Disease

Malte Lenders et al.

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2016)

Review Endocrinology & Metabolism

Immune response to enzyme replacement therapies in lysosomal storage diseases and the role of immune tolerance induction

Priya S. Kishnani et al.

MOLECULAR GENETICS AND METABOLISM (2016)

Article Genetics & Heredity

Long-term effectiveness of agalsidase alfa enzyme replacement in Fabry disease: A Fabry Outcome Survey analysis

Michael Beck et al.

MOLECULAR GENETICS AND METABOLISM REPORTS (2015)

Article Endocrinology & Metabolism

Anti-α-galactosidase A antibody response to agalsidase beta treatment: Data from the Fabry Registry

William R. Wilcox et al.

MOLECULAR GENETICS AND METABOLISM (2012)

Article Transplantation

Globotriaosylsphingosine actions on human glomerular podocytes: implications for Fabry nephropathy

Maria D. Sanchez-Nino et al.

NEPHROLOGY DIALYSIS TRANSPLANTATION (2011)

Article Urology & Nephrology

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

Dominique P. Germain et al.

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2007)

Article Genetics & Heredity

High incidence of later-onset Fabry disease revealed by newborn screening

Marco Spada et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2006)

Article Urology & Nephrology

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

GE Linthorst et al.

KIDNEY INTERNATIONAL (2004)