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Treatment Opportunities in Patients With Metabolic Myopathies
Mette Cathrine Ørngreen
,
John Vissing
Afdeling for Hjerne- og Nervesygdomme
15
Citationer (Scopus)
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Keyphrases
Metabolic Myopathy
100%
Treatment Opportunity
100%
Enzyme Replacement Therapy
60%
Metabolic
40%
McArdle Disease
40%
Gene Expression
20%
Therapeutic Potential
20%
Adult Patients
20%
Potential Treatments
20%
Current Treatment
20%
Treatment Options
20%
Gene Transcription
20%
Carbohydrates
20%
Early Onset
20%
Precipitating Factors
20%
Stiffness
20%
Deficiency Diseases
20%
Molecular Therapy
20%
Skeletal muscle
20%
Gene Therapy
20%
Multiple acyl-CoA Dehydrogenase Deficiency
20%
L-carnitine
20%
New Therapeutics
20%
Dietary Supplements
20%
Energy Failure
20%
Contracture
20%
Targeted Treatment
20%
Diet Therapy
20%
Exercise Therapy
20%
Pompe Disease
20%
Myoglobinuria
20%
Riboflavin
20%
Citric Acid Cycle
20%
Carnitine Deficiency
20%
Exercise-induced Pain
20%
Chaperone Therapy
20%
Riboflavin-responsive
20%
Triheptanoin
20%
Medicine and Dentistry
Myopathy
100%
Enzyme Replacement Therapy
60%
Glycogen Storage Disease Type V
40%
Riboflavin
40%
Gene Expression
20%
Disease
20%
Symptom
20%
Supplementation
20%
Cohort Effect
20%
Genetic Transcription
20%
Nutritional Deficiency
20%
Molecular Therapy
20%
Skeletal Muscle
20%
Gene Therapy
20%
Dietary Supplement
20%
Contracture
20%
Diet Therapy
20%
Citric Acid Cycle
20%
Carnitine
20%
Kinesiotherapy
20%
Myoglobinuria
20%
Glutaric Acidemia Type 2
20%
Glycogen Storage Disease Type II
20%
Pharmacological Treatment
20%
Carnitine Deficiency
20%
Triheptanoin
20%
Pharmacology, Toxicology and Pharmaceutical Science
Myopathy
100%
Replacement Therapy
60%
Riboflavin
40%
Glycogen Storage Disease Type 5
40%
Disease
20%
Symptom
20%
Epidemiology
20%
Nutritional Deficiency
20%
Contracture
20%
Carnitine
20%
Myoglobinuria
20%
Multiple Acyl CoA Dehydrogenase Deficiency
20%
Glycogen Storage Disease Type 2
20%
Carnitine Deficiency
20%
Dietary Supplement
20%
Citrate
20%
Triheptanoin
20%