Renal outcomes of agalsidase beta treatment for Fabry disease: role of proteinuria and timing of treatment initiation
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Title
Renal outcomes of agalsidase beta treatment for Fabry disease: role of proteinuria and timing of treatment initiation
Authors
Keywords
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Journal
NEPHROLOGY DIALYSIS TRANSPLANTATION
Volume 27, Issue 3, Pages 1042-1049
Publisher
Oxford University Press (OUP)
Online
2011-07-30
DOI
10.1093/ndt/gfr420
References
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Related references
Note: Only part of the references are listed.- Dialysis and Transplantation in Fabry Disease: Indications for Enzyme Replacement Therapy
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- Therapeutic goals in the treatment of Fabry disease
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- Enzyme replacement therapy for Fabry's disease
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- Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: an analysis of registry data
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- Fabry disease: progression of nephropathy, and prevalence of cardiac and cerebrovascular events before enzyme replacement therapy
- (2009) R. Schiffmann et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- Stroke in Fabry Disease Frequently Occurs Before Diagnosis and in the Absence of Other Clinical Events
- (2009) Katherine Sims et al. STROKE
- Renal Biopsy Findings in Children and Adolescents With Fabry Disease and Minimal Albuminuria
- (2008) Camilla Tøndel et al. AMERICAN JOURNAL OF KIDNEY DISEASES
- Nephropathy in males and females with Fabry disease: cross-sectional description of patients before treatment with enzyme replacement therapy
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- Kidney biopsy findings in heterozygous Fabry disease females with early nephropathy
- (2008) Carmen Valbuena et al. VIRCHOWS ARCHIV
- Recommendations and guidelines for the diagnosis and treatment of Fabry nephropathy in adults
- (2008) Alberto Ortiz et al. Nature clinical practice. Nephrology
- Females with Fabry disease frequently have major organ involvement: Lessons from the Fabry Registry
- (2007) William R. Wilcox et al. MOLECULAR GENETICS AND METABOLISM
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