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96 Studies found for: Pompe Disease

Terms and Synonyms Searched:

Terms Search Results* Entire Database**
Synonyms
Pompe Disease 96 studies 96 studies
Glycogen Storage Disease Type II 94 studies 94 studies
Acid maltase 32 studies 32 studies
maltase deficiency 30 studies 30 studies
GSD II 26 studies 26 studies
Acid alpha glucosidase 23 studies 23 studies
Glycogenosis 2 14 studies 14 studies
GAA gene 4 studies 4 studies
Glycogen Storage Disease II 4 studies 4 studies
GAA Deficiencies 2 studies 2 studies
Alpha-Glucosidase Deficiencies 2 studies 2 studies
disease pompe's 1 studies 1 studies
Glycogen storage disease type 2 1 studies 1 studies
glycogenosis type II 1 studies 1 studies
Type II glycogen storage disease 1 studies 1 studies
Disease 96 studies 221,690 studies
Disorders 21 studies 78,245 studies
condition 6 studies 29,350 studies
Pompe 93 studies 94 studies

   
-- No studies found
* Number of studies in the search results containing the term or synonym
** Number of studies in the entire database containing the term or synonym

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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
Glycogenosis
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 II
Glycogen Storage Disease Type II