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. 2017 Nov 20;2017(11):CD011539. doi: 10.1002/14651858.CD011539.pub2
Databases Search strategies
CENTRAL #1 glycogen storage disease type II [MeSH descriptor] OR Pompe* disease [All fields] OR acid maltase deficienc* [All fields] OR Generalized Glycogenosis [All fields] OR GAA Deficienc* [All fields] OR glycogen storage disease type II [All fields] OR Alpha‐1,4‐Glucosidase Deficienc* [All fields]
#2 Enzyme Replacement Therapy [MeSH descriptor] OR Enzyme Replacement Therap*[ All fields] OR alglucosidase alfa[All fields] OR Myozyme[All fields] OR ERT[All fields] OR GAA[All fields]
#3 #1 AND #2
PubMed #1 glycogen storage disease type II [mesh] OR Pompe* disease [All fields] OR acid maltase deficienc* [All fields] OR Generalized Glycogenosis [All fields] OR GAA Deficienc* [All fields] OR glycogen storage disease type II [All fields] OR Alpha‐1,4‐Glucosidase Deficienc* [All fields]
#2 Enzyme Replacement Therapy [mesh] OR Enzyme Replacement Therap*[All fields] OR alglucosidase alfa[All fields] OR Myozyme[All fields] OR ERT[All fields] OR GAA[All fields]
#3 #1 AND #2
Embase (Ovid) #1 glycogen storage disease type 2 [Map Term] OR Pompe* disease [All fields] OR acid maltase deficienc* [All fields] OR Generalized Glycogenosis [All fields] OR GAA Deficienc* [All fields] OR glycogen storage disease type II [All fields] OR Alpha‐1,4‐Glucosidase Deficienc* [All fields]
#2 Enzyme Replacement Therapy [Map Term] OR Enzyme Replacement Therap*[ All fields] OR alglucosidase alfa[All fields] OR Myozyme[All fields] OR ERT[All fields] OR GAA[All fields]
#3 #1 AND #2
LILACS #1 Pompe$ disease [All fields] OR acid maltase deficienc$ [All fields] OR Generalized Glycogenosis [All fields] OR GAA Deficienc$ [All fields] OR glycogen storage disease type II [All fields] OR Alpha‐1,4‐Glucosidase Deficienc$ [All fields]
#2 Enzyme Replacement Therap$ [ All fields] OR alglucosidase alfa[All fields] OR Myozyme[All fields] OR ERT[All fields] OR GAA[All fields]
#3 #1 AND #2
WHO ICTRP Pompe
ClinicalTrials.gov Pompe
Genzyme Pompe