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91 Studies found for:
"Glycogen Storage Disease Type II" OR "Pompe disease"
Recognized Terms and Synonyms:
Glycogen Storage Disease Type II:   91 studies
Pompe disease
Acid maltase
maltase deficiency
GSD II
Glycogenosis 2
Acid alpha-glucosidase
Glycogen Storage Disease II
Alpha-Glucosidase Deficiencies
GAA gene
disease pompe's
Glycogen storage disease type 2
glycogenosis type II
2 glycogenosis
Deficiency of alpha-glucosidase
Deficiency of amyloglucosidase
Deficiency of gamma-amylase
Deficiency of glucoamylase
Deficiency of glucoinvertase
Deficiency of glucosidosucrase
Deficiency of maltase
GAA Deficiencies
Generalised glycogenosis
Generalized Glycogenoses
GSD type II
GSD2
maltase acid deficiency
Type II glycogen storage disease
Pompe disease:   91 studies
Glycogen Storage Disease Type II
Acid maltase
maltase deficiency
GSD II
Glycogenosis 2
Acid alpha-glucosidase
Glycogen Storage Disease II
Alpha-Glucosidase Deficiencies
GAA gene
disease pompe's
Glycogen storage disease type 2
glycogenosis type II
2 glycogenosis
Aglucosidase alfa
Alpha-1,4-glucosidase deficiency
Cardiomegalia glycogenica diffusa
Deficiency of alpha-glucosidase
Deficiency of amyloglucosidase
Deficiency of gamma-amylase
Deficiency of glucoamylase
Deficiency of glucoinvertase
Deficiency of glucosidosucrase
Deficiency of lysosomal alpha-glucosidase
Deficiency of maltase
GAA Deficiencies
Generalised glycogenosis
Generalized Glycogenoses
Glycogen heart disease
GSD type II
GSD2
maltase acid deficiency
Type II glycogen storage disease
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A acid alpha-glucosidase
Acid Maltase
Acid Maltase Deficiency
alglucosidase
alglucosidase alfa
alpha-
acid alpha-glucosidase
alpha-glucosidase
acid alpha-glucosidase
alglucosidase alfa
B Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
C carbohydrate
Carbohydrate Metabolism
D Deficiency
Acid Maltase Deficiency
Maltase Deficiency
Acid Maltase Deficiency
Disease Type
Glycogen Storage Disease Type II
Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Diseases, Metabolic
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Diseases, Nervous System
Disease Type
Glycogen Storage Disease Type II
Glycogen Storage Disease
Glycogen Storage Disease Type II
Lysosomal Storage Diseases
Nervous System Diseases
Pompe Disease
Storage Diseases
Glycogen Storage Disease
Glycogen Storage Disease Type II
Lysosomal Storage Diseases
E enzyme replacement therapy
Errors
Metabolism, Inborn Errors
ERT
G GAA
Genzyme
glucosidase
acid alpha-glucosidase
alpha-glucosidase
acid alpha-glucosidase
Glycogen
Glycogen Storage Disease
Glycogen Storage Disease Type II
GSD
GSD-II
I Infantile
infantile-onset
L late
late-onset
Lysosomal
Lysosomal Storage Diseases
M Maltase
Acid Maltase
Acid Maltase Deficiency
Maltase Deficiency
Acid Maltase Deficiency
Metabolic
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Diseases, Metabolic
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Metabolism
Carbohydrate Metabolism
Metabolism, Inborn Errors
muscle
Myozyme
N Nervous System Diseases
O onset
infantile-onset
late-onset
P Pompe Disease
R replacement therapy
enzyme replacement therapy
rhGAA
S Storage
Glycogen Storage Disease
Glycogen Storage Disease Type II
Lysosomal Storage Diseases
Storage Diseases
Glycogen Storage Disease
Glycogen Storage Disease Type II
Lysosomal Storage Diseases
T Type
Disease Type
Glycogen Storage Disease Type II
Type II
Glycogen Storage Disease Type II