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Molecular update and therapeutic trials in muscle disorders of glycogen and lipid metabolism
Corrado Angelini
Istituto di Neuroriabilitazione Motoria San Camillo
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Medicine & Life Sciences
Glycogen Storage Disease Type II
100%
acyl-CoA transferase
92%
Myopathy with Abnormal Lipid Metabolism
83%
Muscular Diseases
74%
Glycogen
72%
Myoglobinuria
69%
Lipid Metabolism
66%
Carnitine
55%
Cardiomyopathies
45%
Solute Carrier Family 22 Member 5
43%
Fatty Acids
39%
Systemic carnitine deficiency
39%
Enzymes
37%
Phosphorylases
32%
High-Protein Diet
32%
Muscle Cramp
30%
alpha-Glucosidases
30%
Exercise
29%
Cardiomegaly
24%
Muscle Weakness
24%
Hypoglycemia
22%
Respiratory Insufficiency
21%
Mitochondria
19%
Skeletal Muscle
18%
Extremities
17%
Lipids
15%
Glucose
14%
Muscles
13%
Therapeutics
11%
Genes
9%