Massive accumulation of globotriaosylceramide in various tissues from a Fabry patient with a high antibody titer against alpha-galactosidase A after 6 years of enzyme replacement therapy
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology
Reference23 articles.
1. Enzyme replacement therapy for Fabry disease, an inherited nephropathy;Desnick;Clin. Nephrol.,2002
2. Clinical manifestations and natural history of Japanese heterozygous females with Fabry disease;Kobayashi;J. Inherit. Metab. Dis.,2008
3. Anti-α-galactosidase A antibody response to agalsidase beta treatment: data from the Fabry Registry;Wilcox;Mol. Genet. Metab.,2012
4. Generation of one set of murine monoclonal antibodies specific for globo-series glycolipids: evidence for differential distribution of the glycolipids in rat small intestine;Kotani;Arch. Biochem. Biophys.,1994
5. Immunofluorescence imaging diagnosis of Fabry heterozygotes using confocal laser scanning microscopy;Itoh;Clin. Genet.,1993
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