One Year of Enzyme Replacement Therapy Reduces Globotriaosylceramide Inclusions in Podocytes in Male Adult Patients with Fabry Disease

Author:

Najafian Behzad,Tøndel Camilla,Svarstad Einar,Sokolovkiy Alexey,Smith Kelly,Mauer Michael

Funder

Genzyme

National Institute of Neurological Disorders and Stroke

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference50 articles.

1. Fabry's disease: enzymatic diagnosis of hemizygotes and heterozygotes. Alpha-galactosidase activities in plasma, serum, urine, and leukocytes;RJ Desnick;J Lab Clin Med,1973

2. Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 98 hemizygous males;KD MacDermot;J Med Genet,2001

3. Globotriaosylceramide accumulation in the Fabry kidney is cleared from multiple cell types after enzyme replacement therapy;BL Thurberg;Kidney Int,2002

4. Sustained, long-term renal stabilization after 54 months of agalsidase beta therapy in patients with Fabry disease;DP Germain;J Am Soc Nephrol,2007

5. Agalsidase-beta therapy for advanced Fabry disease: a randomized trial;M Banikazemi;Ann Intern Med,2007

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