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5 in total

1. Enzyme therapy in Fabry disease: differential in vivo plasma clearance and metabolic effectiveness of plasma and splenic alpha-galactosidase A isozymes.

Authors: R J Desnick; K J Dean; G Grabowski; D F Bishop; C C Sweeley
Journal: Proc Natl Acad Sci U S A Date: 1979-10 Impact factor: 11.205

2. Lysosomal alpha-galactosidase in endothelial cell cultures established from a Fabry hemizygous and normal umbilical veins.

Authors: L Hasholt; S A Sørensen
Journal: Hum Genet Date: 1986-01 Impact factor: 4.132

3. Lysosomal glycosphingolipid storage in chloroquine-induced alpha-galactosidase-deficient human endothelial cells with transformation by simian virus 40: in vitro model of Fabry disease.

Authors: M Inagaki; T Katsumoto; E Nanba; K Ohno; S Suehiro; K Takeshita
Journal: Acta Neuropathol Date: 1993 Impact factor: 17.088

4. Establishment and characterization of Fabry disease endothelial cells with an extended lifespan.

Authors: Jin-Song Shen; Xing-Li Meng; Raphael Schiffmann; Roscoe O Brady; Christine R Kaneski
Journal: Mol Genet Metab Date: 2007-07-17 Impact factor: 4.797

Review 5. Ion channels and pain in Fabry disease.

Authors: Carina Weissmann; Adriana A Albanese; Natalia E Contreras; María N Gobetto; Libia C Salinas Castellanos; Osvaldo D Uchitel
Journal: Mol Pain Date: 2021 Jan-Dec Impact factor: 3.395

5 in total