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alglucerase

Known as: alglucerase [Chemical/Ingredient] 
 
National Institutes of Health

Papers overview

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2009
2009
Purpose: To determine whether enzyme therapy with imiglucerase/alglucerase demonstrates dose-response relationships with doses… Expand
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Highly Cited
1999
Highly Cited
1999
Alglucerase, a macrophage-targeted enzyme replacement therapy for Gaucher disease, has been successfully used for several years… Expand
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1997
1997
A marked elevation in plasma chitotriosidase (chitinase) activity has recently been observed in patients with Gaucher disease… Expand
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1996
1996
OBJECTIVES The incidence and severity of growth retardation in children with type 1 Gaucher disease and the response to enzyme… Expand
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1996
1996
Gaucher disease is an autosomal-recessive disorder that is caused by a deficiency of the enzyme glucocerebrosidase and results in… Expand
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1995
1995
Previous studies have shown that enzyme supplementation therapy with alglucerase for type 1 Gaucher's disease is effective at… Expand
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1995
1995
One hundred nineteen patients with Gaucher disease were examined in the past 13 years. Of these 45 were examined 3 or more times… Expand
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Highly Cited
1993
Highly Cited
1993
Gaucher disease is the most frequent lysosomal storage disease and the most prevalent genetic disease among the Ashkenazi Jews (q… Expand
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1993
1993
Mannose-terminated glucocerebrosidase (alglucerase; Ceredase) was designed for enzyme replacement therapy in Gaucher disease to… Expand
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1992
1992
BACKGROUND Alglucerase (Ceredase) provides effective enzyme-replacement treatment for patients with Gaucher's disease, but at the… Expand
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