70 studies found for:    "Glycogen Storage Disease Type II" OR "Pompe disease"
Found 70 studies with search of:   "Glycogen Storage Disease Type II" OR "Pompe disease"
Recognized Terms and Synonyms:
Glycogen Storage Disease Type II:   70 studies
2 glycogenosis
Acid alpha-glucosidase
Acid maltase
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
GAA gene
GSD II
GSD type II
GSD2
Generalised glycogenosis
Generalized Glycogenoses
Glycogen Storage Disease II
Glycogen storage disease type 2
Glycogenosis 2
Pompe disease
Type II glycogen storage disease
alpha-Glucosidase deficiency
disease pompe's
glycogenosis type II
maltase acid deficiency
maltase deficiency
Pompe disease:   70 studies
2 glycogenosis
Acid alpha-glucosidase
Acid maltase
Aglucosidase alfa
Alpha-1,4-glucosidase acid deficiency
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
GAA gene
GSD II
GSD type 2
GSD type II
GSD2
Generalised glycogenosis
Generalized Glycogenoses
Generalized glycogen storage disease of infants
Glycogen Storage Disease II
Glycogen Storage Disease Type II
Glycogen heart disease
Glycogen storage disease type 2
Glycogenosis 2
Glycogenosis type 2
Type II glycogen storage disease
alpha-Glucosidase deficiency
disease pompe's
glycogenosis type II
maltase acid deficiency
maltase deficiency
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A Acid Maltase
Acid Maltase Deficiency
B Brain Diseases
Brain Diseases, Metabolic
C 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
Diseases, Metabolic
Brain Diseases, Metabolic
Diseases, Nervous System
Disease Type
Glycogen Storage Disease Type II
Glycogen Storage Disease
Glycogen Storage Disease Type II
Lysosomal Storage Diseases
Pompe Disease
Storage Diseases
Glycogen Storage Disease
Glycogen Storage Disease Type II
Lysosomal Storage Diseases
E Errors
Metabolism, Inborn Errors
G GAA
GSD
GSD-II
Genzyme
Glycogen
Glycogen Storage Disease
Glycogen Storage Disease Type II
I Infantile
L Lysosomal
Lysosomal Storage Diseases
M Maltase
Acid Maltase
Acid Maltase Deficiency
Maltase Deficiency
Acid Maltase Deficiency
Metabolism, Inborn Errors
Myozyme
P Pompe Disease
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 II
Glycogen Storage Disease Type II
A acid alpha-glucosidase
alglucosidase
alglucosidase alfa
alpha
acid alpha-glucosidase
alpha-glucosidase
acid alpha-glucosidase
alglucosidase alfa
E enzyme replacement therapy
G glucosidase
acid alpha-glucosidase
alpha-glucosidase
acid alpha-glucosidase
L late
M muscle
O onset
R rhGAA