A skeletal-muscle disorder associated with intermittent symptoms and a possible defect of lipid metabolism

N Engl J Med. 1970 Mar 26;282(13):697-704. doi: 10.1056/NEJM197003262821301.
No abstract available

MeSH terms

  • Adolescent
  • Alanine Transaminase / blood
  • Aspartate Aminotransferases / blood
  • Biopsy
  • Carbohydrate Metabolism
  • Creatine Kinase / blood
  • Dietary Fats
  • Diseases in Twins*
  • Fatty Acids / metabolism
  • Female
  • Fructose-Bisphosphate Aldolase / blood
  • Histocytochemistry
  • Humans
  • Insulin / blood
  • Ketone Bodies / blood
  • Ketone Bodies / urine
  • L-Lactate Dehydrogenase / blood
  • Ligases / metabolism
  • Lipid Metabolism, Inborn Errors / complications*
  • Lipid Metabolism, Inborn Errors / diagnosis
  • Lipid Metabolism, Inborn Errors / genetics
  • Muscles / analysis
  • Muscles / enzymology
  • Muscles / metabolism
  • Muscles / pathology
  • Muscular Diseases / etiology*
  • Muscular Diseases / genetics
  • Myoglobinuria / complications
  • Pain
  • Physical Exertion
  • Triglycerides

Substances

  • Dietary Fats
  • Fatty Acids
  • Insulin
  • Ketone Bodies
  • Triglycerides
  • L-Lactate Dehydrogenase
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • Creatine Kinase
  • Fructose-Bisphosphate Aldolase
  • Ligases