Glycogen Storage Disease Type V

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  Subject Areas on Research

  • Adenovirus-mediated delivery into myocytes of muscle glycogen phosphorylase, the enzyme deficient in patients with glycogen-storage disease type V. 
  • Asymptomatic McArdle's disease associated with hyper-creatine kinase-emia and absence of myophosphorylase. 
  • Late-onset Mcardle's disease with unusual electromyographic findings. 
  • Noncardiogenic pulmonary edema and rhabdomyolsis after protamine administration in a patient with unrecognized McArdle's disease.