α-Glucosidase deficiency in generalized glycogen-storage disease (Pompe's disease)

Ítems similars

• Glycogen storage disease type II (Pompe disease) in children
  per: A. N. Semyachkina, et al.
  Publicat: (2016-03-01)
• Therapeutic approaches in glycogen storage disease type II/pompe disease
  per: Schoser, Benedikt, et al.
  Publicat: (2008)
• Neuropathological and neurochemical aspects of generalized glycogen storage disease
  per: Crome, L., et al.
  Publicat: (1963)
• Glycosylation-independent Lysosomal Targeting of Acid α-Glucosidase Enhances Muscle Glycogen Clearance in Pompe Mice
  per: Maga, John A., et al.
  Publicat: (2013)
• Glycogen phosphorylase and its converter enzymes in haemolysates of normal human subjects and of patients with type VI glycogen-storage disease. A study of phosphorylase kinase deficiency.
  per: Lederer, B, et al.
  Publicat: (1975)