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Treatment Opportunities in Patients With Metabolic Myopathies
Mette Cathrine Ørngreen,
John Vissing
Institut for Klinisk Medicin
8
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Medicin og biovidenskab
Carbohydrates
8%
Carnitine
11%
Citric Acid Cycle
11%
Contracture
10%
Deficiency Diseases
12%
Dietary Supplements
9%
Enzyme Replacement Therapy
36%
Enzymes
5%
Exercise
6%
Exercise Therapy
11%
Fatigue
7%
Fats
6%
Gene Expression
5%
Genes
3%
Genetic Therapy
17%
Glycogen Storage Disease Type II
13%
Glycogen Storage Disease Type V
30%
Multiple Acyl Coenzyme A Dehydrogenase Deficiency
16%
Muscular Diseases
100%
Myoglobinuria
13%
Pain
5%
Pharmacology
6%
Precipitating Factors
11%
Riboflavin
23%
Skeletal Muscle
7%
Sucrose
9%
Systemic carnitine deficiency
15%
Therapeutics
15%
triheptanoin
18%