Working...
ClinicalTrials.gov
ClinicalTrials.gov Menu
Open or close the search fields display
103 Studies found for: Pompe Disease

Terms and Synonyms Searched:

Terms Search Results* Entire Database**
Synonyms
Pompe Disease 103 studies 103 studies
Glycogen Storage Disease Type II 101 studies 101 studies
Acid maltase 30 studies 30 studies
maltase deficiency 29 studies 29 studies
GSD II 26 studies 26 studies
Glycogenosis 2 14 studies 14 studies
Acid alpha glucosidase 8 studies 8 studies
Glycogen Storage Disease II 3 studies 3 studies
Alpha-Glucosidase Deficiencies 3 studies 3 studies
Glycogen storage disease type 2 2 studies 2 studies
GAA gene 1 studies 1 studies
disease pompe's 1 studies 1 studies
GAA Deficiencies 1 studies 1 studies
glycogenosis type II 1 studies 1 studies
Disease 103 studies 226,572 studies
Disorders 18 studies 81,701 studies
condition 1 studies 10,928 studies
Pompe 100 studies 101 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

Related Terms:

Click on a related term to refine your search.
This will narrow your search by adding an additional search term.
If your search becomes too narrow (finds too few studies), broaden it by removing search terms with the Modify Search page.

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
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 II
Glycogen Storage Disease Type II