Pages that link to "Q73881198"

The following pages link to Amylo-1, 6-glucosidase in muscle tissue in generalized glycogen storage disease (Q73881198):

Displaying 17 items.

• Different clinical aspects of debrancher deficiency myopathy (Q33712716) (← links)
• INHERITED ENZYME DEFECTS: A REVIEW. (Q35393479) (← links)
• The clinical course of glycogen disease (Q35895415) (← links)
• Glycogen disease (Q36049670) (← links)
• Characterization of a canine model of glycogen storage disease type IIIa (Q36359220) (← links)
• ACTION OF AMYLO-1,6-GLUCOSIDASE ON LOW MOLECULAR WEIGHT SUBSTRATES AND THE ASSAY OF THIS ENZYME IN GLYCOGEN STORAGE DISEASE. (Q36396375) (← links)
• Hypoglycaemia in childhood (Q36769565) (← links)
• Skeletal muscle glycogenosis: an investigation of two dissimilar cases (Q39414224) (← links)
• A survey of some hereditary metabolic diseases (Q40829844) (← links)
• THE EFFECT OF PORTACAVAL TRANSPOSITION ON CARBOHYDRATE METABOLISM: EXPERIMENTAL AND CLINICAL OBSERVATIONS (Q41414458) (← links)
• The significance of glucagon. (Q42173865) (← links)
• Biochemical investigations of a case of glycogenstorage disease (von Gierke's disease). (Q42961767) (← links)
• Claude Bernard and the discovery of glycogen; a century of retrospect. (Q52498168) (← links)
• Myopathy due to acid maltase deficiency. Pompe's disease in adolescence and adult (author's transl) (Q69042678) (← links)
• First trimester prenatal diagnosis of glycogen storage disease type III (Q69256425) (← links)
• Type 3 a glycogenosis. A biochemical and ultrastructural study (Q71105036) (← links)
• [Neuromuscular form of glycogen storage disease] (Q78450219) (← links)