Hepatic glycogen storage diseases: pathogenesis, clinical symptoms and therapeutic management

Lignende værker

• Over 20-Year Follow-up of Patients with Hepatic Glycogen Storage Diseases: Single-Center Experience
  af: Edyta Szymańska, et al.
  Udgivet: (2020-05-01)
• Over 20-Year Follow-up of Patients with Hepatic Glycogen Storage Diseases: Single-Center Experience
  af: Szymańska, Edyta, et al.
  Udgivet: (2020)
• The potential of dietary treatment in patients with glycogen storage disease type IV
  af: Derks, Terry G. J., et al.
  Udgivet: (2020)
• Variable clinical presentation of glycogen storage disease type IV: from severe hepatosplenomegaly to cardiac insufficiency. Some discrepancies in genetic and biochemical abnormalities
  af: Szymańska, Edyta, et al.
  Udgivet: (2017)
• Pediatric patient with hyperketotic hypoglycemia diagnosed with glycogen synthase deficiency due to the novel homozygous mutation in GYS2
  af: Szymańska, Edyta, et al.
  Udgivet: (2015)