glycogen storage disease type ii; Generalized Glycogenosis; Glycogenosis 2; Pompe Disease; Acid Maltase Deficiency Disease; Lysosomal alpha-1,4-Glucosidase Deficiency Disease

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Symptoms:

	Active principles	Rating	Bibliogr.
1	Glucan 1,4-alpha-Glucosidase	100	+
2	alpha-Glucosidases	81	+
3	Creatine Kinase, MM Form	32	+
4	Complement C2	29	+
5	Glucosidases	23	+
6	Glycogen	18	+
7	Phosphorylase Kinase	10	+
8	Glucose-6-Phosphatase	6	+
9	Starch	6	+
10	Receptor, IGF Type 2	4	+
11	Glucose-6-Phosphate	4	+
12	Chloromercuribenzoates	3	+
13	1-Deoxynojirimycin	3	+
14	Dietary Proteins	2	+
15	Recombinant Proteins	2	+
16	Liver Glycogen	2	+
17	Granulocyte Colony-Stimulating Factor	2	+
18	Glycogen Synthase	1	+
19	Glucosylceramidase	1	+
20	Glycogen Debranching Enzyme System	1	+
21	Phosphorylase b	1	+
22	Oligo-1,6-Glucosidase	1	+
23	Clenbuterol	1	+
24	Enzymes	1	+
25	Phosphorylase a	1	+
26	Lactates	1	+
27	Sucrase	1	+
28	Oligosaccharides	1	+
29	Dietary Carbohydrates	1	+
30	Blood Glucose	1	+
31	Glycogen Phosphorylase	1	+
32	Glucose	1	+
33	Disaccharidases	1	+

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