FUTURE TRENDS IN THE INVESTIGATION OF GLYCOGEN STORAGE DISEASE.
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Brain Chemistry↗
Biomedical subjects
H G HERS
Publications and source records attributed to H G HERS.
INBORN LYSOSOMAL DISEASES.
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Glycogen Storage Disease↗
[CONGENITAL LYSOSOMIAL DISEASES].
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Glycogen Storage Disease↗
[ULTRASTRUCTURE OF THE HEPATIC CELLS IN HURLER'S DISEASE (GARGOYLISM)].
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Cytodiagnosis↗
[ENZYMATIC STUDY OF GLYCOGENOSIS].
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Child↗
AN ELECTRON MICROSCOPIC AND BIOCHEMICAL STUDY OF TYPE II GLYCOGENOSIS.
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Acid Phosphatase↗
alpha-Glucosidase deficiency in generalized glycogenstorage disease (Pompe's disease).
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Glucosidases↗
Tissue fractionation studies. 16. Intracellular distribution and properties of alpha-glucosidases in rat liver.
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Cytoplasm↗
[HUMAN BIOCHEMICAL GENETICS].
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Biochemical Phenomena↗
[A new method for the detection of congenital galactosemia].
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Galactose↗
[Increase of activity of glucose-6-phosphatase in intolerance to fructose].
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Fructose↗
[Anomaly of hepatic aldolase in intolerance to fructose].
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Fructose↗
On the conversion of fructose to glucose by guinea pig intestine.
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Carbohydrate Metabolism↗
[Aldose reductase].
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Aldehyde Reductase↗
[The mechanism of the formation of seminal fructose and fetal fructose].
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Carbohydrate Metabolism↗
A note on glucose-6-phosphatase activity of blood serum.
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Glucose-6-Phosphatase↗
[Enzymatic studies of hepatic fragments; application to the classification of glycogenoses].
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Glycogen Storage Disease↗