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Symptoms:
Glycogen Storage Disease Type IV; Amylopectinosis; Andersen Disease; Brancher Deficiency; Glycogenosis 4
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Hierarchical
More information
disease
;
glycogen
;
glycogen storage disease
;
glycogen storage disease type iv
Active principles
Rating
Bibliogr.
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1
alpha-Glucosidases
100
+
2
Glucan 1,4-alpha-Glucosidase
84
+
3
Creatine Kinase, MM Form
48
+
4
Glycogen
42
+
5
Phosphorylase Kinase
32
+
6
Glucose-6-Phosphatase
30
+
7
Starch
28
+
8
Glucose-6-Phosphate
21
+
9
Aerosols
13
+
10
Liver Glycogen
10
+
11
Granulocyte Colony-Stimulating Factor
9
+
12
Glycogen Synthase
9
+
13
Collagen Type IV
8
+
14
1-Deoxynojirimycin
8
+
15
Glucosylceramidase
7
+
16
Recombinant Proteins
6
+
17
Phosphorylase b
6
+
18
Phosphorylase a
5
+
19
Lactates
5
+
20
Dietary Carbohydrates
5
+
21
Glucose
4
+
22
Hexosaminidases
4
+
23
Blood Glucose
4
+
24
Lactic Acid
3
+
25
Glycogen Phosphorylase
3
+
26
Albuterol
3
+
27
Glycogen Synthase Kinase 3
3
+
28
Glycosphingolipids
3
+
29
Glucosyltransferases
3
+
30
Glucuronidase
2
+
31
von Willebrand Factor
2
+
32
Glucose Transport Proteins, Facilitative
2
+
33
Deamino Arginine Vasopressin
2
+
34
Cerebroside-Sulfatase
1
+
35
Glucosylceramides
1
+
36
Insulin
1
+
37
Sterol Esterase
1
+
38
Hexosaminidase B
1
+
39
Hydrolases
1
+
40
Hexosaminidase A
1
+
41
Myosin Type IV
1
+
42
Codon, Nonsense
1
+
43
Sulfur Isotopes
1
+
44
Mannosephosphates
1
+
45
beta-N-Acetylhexosaminidases
1
+
46
Triglycerides
1
+
47
Phosphorylases
1
+
48
Molecular Chaperones
1
+
49
Iduronidase
1
+
50
Glycosaminoglycans
1
+
51
alpha-Galactosidase
1
+
52
Glycogen Synthase Kinases
1
+
53
alpha-Mannosidase
1
+
54
Enzymes
1
+
55
Factor VIII
1
+
56
Phytanic Acid
1
+
57
Glucosephosphates
1
+
58
Dextranase
1
+
59
beta-Glucosidase
1
+
60
Receptor, IGF Type 2
1
+
61
Ristocetin
1
+
62
Naphthol AS D Esterase
1
+
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