Skeletal muscle glycogenosis: an investigation of two dissimilar cases

This publication has 22 references indexed in Scilit:

• Glycogen storage disease of the muscles: Report of a case with unusual features
  The Journal of Pediatrics, 1962
• Sources of error in the biochemical diagnosis of muscular dystrophy
  Journal of Neurology, Neurosurgery & Psychiatry, 1962
• McARDLE'S SYNDROME: PHOSPHORYLASE-DEFICIENT MYOPATHY
  The Lancet, 1962
• A metabolic myopathy due to absence of muscle phosphorylase
  The American Journal of Medicine, 1961
• Serum Enzyme Activity in Muscular Dystrophy
  BMJ, 1960
• CHRONIC PROGRESSIVE MYOPATHY WITH MYOGLOBINURIA: DEMONSTRATION OF A GLYCOGENOLYTIC DEFECT IN THE MUSCLE*
  Journal of Clinical Investigation, 1959
• DISEASES OF GLYCOGEN STORAGE WITH SPECIAL REFERENCE TO THE CARDIAC TYPE OF GENERALIZED GLYCOGENOSIS
  Annals of the New York Academy of Sciences, 1959
• A uridine coenzyme-linked pathway of glycogen synthesis in muscle
  Biochimica et Biophysica Acta, 1958
• An improved microdiffusion procedure for the determination of lactic acid
  The Analyst, 1958
• The Molecular Structure of Glycogens
  Published by Elsevier ,1957