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Myozyme

National Institutes of Health

Papers overview

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2020
2020
2020
The alglucosidase alfa (Myozyme®) Safety Information Packet (“previous SIP”) was updated to improve readability and content… 
2013
2013
With dabigatran and rivaroxaban, two new promising anticoagulants (NOACs) are now approved and available in most countries… 
2013
2013
Pompe disease is an autosomal recessive inherited glycogen storage disease, usually respiratory muscles, cardiac muscle and… 
2012
2012
Oxyrane and BioMarin have separately reported on their next-generation enzyme replacement therapies for Pompe's disease. Both… 
Review
2009
Review
2009
Pompe disease is a rare autosomal recessive lysosomal storage disease caused by deficiency of acid-a-glucosidase (GAA). This…