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Replagal

National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Background: Fabry disease is a rare X-linked lysosomal storage disease caused by defective activity of the lysosomal enzyme… 
Review
2014
Review
2014
Enzyme replacement therapies substitute particular enzymes in individuals who have deficient or absent levels of enzymatic… 
2012
2012
Agalsidasa; Malaltia de Fabry; Revisio sistematica; Agalsidase; Fabry's disease; Clinical trial; Enfermedad de Fabry; Revision… 
Highly Cited
2009
Highly Cited
2009
Purpose: Although Fabry disease is X linked and considered to affect primarily male hemizygotes, female heterozygotes may… 
2007
2007
  • G. Pastores
  • 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… 
Review
2004
Review
2004
Two virtually identical products have been developed for enzyme replacement therapy for the treatment of Fabry disease, which is… 
2003
2003
Enzyme therapy has proven safe and effective in preventing and reversing many manifestations in patients with Gaucher disease. On… 
2003
2003
Aim: To study the prevalence of peripheral vestibular deficit in male and female patients with Fabry disease and to assess the… 
Highly Cited
2003
Highly Cited
2003
Summary: Fabry disease is an X-linked glycosphingolipid storage disorder caused by a deficiency of α-galactosidase A. Affected…