Longitudinal characterization of Gaac.1826dupA mice reveals the cardiac, myopathic and biochemical phenotypes of Pompe disease

Lignende værker

• The Action of Recombinant Human Lysosomal α-Glucosidase (rhGAA) on Human Liver Glycogen: Pathway to Complete Degradation
  af: Allen K. Murray
  Udgivet: (2021-12-01)
• Validation and standardization of a fluorometric method for alpha glucosidase activity assay in the detection of Pompe disease
  af: Armin Mokhtariye, et al.
  Udgivet: (2023-06-01)
• Interplay between mitochondrial dysfunction and lysosomal storage: challenges in genetic metabolic muscle diseases with a focus on infantile onset Pompe disease
  af: Mengjiao Zhang, et al.
  Udgivet: (2024-02-01)
• Pharmacological Chaperone Therapy for Pompe Disease
  af: Marc Borie-Guichot, et al.
  Udgivet: (2021-11-01)
• Newborn Screening for Pompe Disease: Pennsylvania Experience
  af: Can Ficicioglu, et al.
  Udgivet: (2020-11-01)