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human GAA protein (Myozyme) Summary

Description: Defects in the gene for this protein cause glycogen storage disease II, also known as Pompe disease, RefSeq NM_000152

Also Known As: Myozyme; alglucosidase alfa; GAA protein, human; Genzyme brand of Recombinant human alglucosidase alfa; LYAG protein, human Show All >>

Networked: 96 relevant articles (23 outcomes, 20 trials/studies) for this Drug

Key Diseases for which human GAA protein is Relevant

  1. Glycogen Storage Disease Type II (Pompe's Disease) : 19 outcomes 16 studies in 87 results
  2. Cardiomyopathies (Cardiomyopathy) : 6 outcomes 4 studies in 9 results
  3. Muscular Diseases (Myopathy) : 1 outcome 1 study in 2 results
  4. Anaphylaxis (Anaphylactic Shock) : 1 study in 3 results
  5. Hypersensitivity (Allergy) : 1 study in 2 results
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Drugs Related to human GAA protein

  1. human GAA protein (Myozyme)
  2. alpha-Glucosidases (Acid Maltase)
  3. Glucosidases
  4. Antibodies
  5. Ligands
  6. Glycogen
  7. Mannose (D-Mannose)
  8. Immunoglobulins (Immunoglobulin)
  9. Immunoglobulin G (IgG)
  10. Immunoglobulin E (IgE)
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Therapies Related to human GAA protein

  1. Enzyme Replacement Therapy
  2. Mechanical Ventilators (Ventilator)
  3. Enzyme Therapy
  4. Immunomodulation
  5. Drug-Eluting Stents
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