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124 Studies found for: "glycogen storage disease type IX" OR "Glycogen Storage Disease"

Terms and Synonyms Searched:

Terms Search Results* Entire Database**
Synonyms
glycogen storage disease type IX 1 studies 1 studies
Phosphorylase Kinase Deficiency 1 studies 1 studies
Glycogen Storage Disease 124 studies 124 studies
Glycogenoses 21 studies 21 studies
glycogen storage disorder 4 studies 4 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
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
Genetic Diseases, Inborn
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 enzyme replacement therapy
Errors
Metabolism, Inborn Errors
G GAA
Genetic Diseases, Inborn
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
O onset
infantile-onset
late-onset
P Pompe Disease
R 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