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agalsidase alfa

Known as: recombinant alpha-galactosidase A 
National Institutes of Health

Related topics

Related topics

3 relations

Broader (2)

ALPHA-D-GALACTOSIDASE ENZYMEIsoenzymes

Narrower (1)

Replagal

Papers overview

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Review
2015
Review
2015
Fabry disease: a review of current enzyme replacement strategies
Introduction: Fabry disease (OMIM 301500) is an X linked lysosomal storage disorder caused by deficiency of α galactosidase A… 
2010
2010
Enzymersatztherapie bei Morbus Fabry
ZusammenfassungDer Morbus Fabry ist die einzige lysosomale Speicherkrankheit, bei welcher 2 verschiedene Präparate (Agalsidase… 
2007
2007
Agalsidase alfa (Replagal™) in the treatment of Anderson-Fabry disease
  • G. Pastores
  • Biologics : targets & therapy
  • 2007
  • Corpus ID: 17351645
Anderson-Fabry disease (AFD) is an X-linked storage disorder caused by a deficiency of the lysosomal hydrolase a-galactosidase A… 
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