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Enzyme Therapy

Known as: Enzyme Therapies, Therapies, Enzyme, Therapy, Enzyme 
The use of enzymes to correct metabolic and physiological processes.
National Institutes of Health

Papers overview

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Highly Cited
2011
Highly Cited
2011
BACKGROUND In Gaucher disease (GD), acid-β-glucosidase (GBA1) gene mutations result in defective glucocerebrosidase and variable… Expand
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Highly Cited
2008
Highly Cited
2008
Gaucher's disease continues to be a model for applications of molecular medicine to clinical delineation, diagnosis, and… Expand
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Highly Cited
2007
Highly Cited
2007
BACKGROUND & AIMS Malnutrition persists in most patients with chronic pancreatitis despite an adequate clinical response to oral… Expand
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Highly Cited
2007
Highly Cited
2007
Treatment of brain disease with recombinant proteins is difficult due to the blood-brain barrier. As an alternative to direct… Expand
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Highly Cited
2004
Highly Cited
2004
BACKGROUND Fabry disease is an X-linked inherited disorder that is caused by excessive lysosomal globotriaosylceramide (CTH… Expand
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Highly Cited
2004
Highly Cited
2004
Gaucher disease is characterized by storage of glucosylceramide in lysosomes of tissue macrophages as the result of an autosomal… Expand
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Highly Cited
2002
Highly Cited
2002
Background—Although studies have suggested that “late-onset” hypertrophic cardiomyopathy (HCM) may be caused by sarcomeric… Expand
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Highly Cited
2002
Highly Cited
2002
Immune reconstitution in ADA-SCID after PBL gene therapy and discontinuation of enzyme replacement 
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Highly Cited
2001
Highly Cited
2001
Purpose: Infantile glycogen storage disease type II (GSD-II) is a fatal genetic muscle disorder caused by deficiency of acid… Expand
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Highly Cited
2001
Highly Cited
2001
Purpose: Infantile glycogen storage disease type II (GSD-II) is a fatal genetic muscle disorder caused by deficiency of acid… Expand
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