subject area of
- Aerobic training as an adjunctive therapy to enzyme replacement in Pompe disease Academic Article
- Characterization of tracheobronchomalacia in infants with hypophosphatasia Academic Article
- Combined aerobic exercise and enzyme replacement therapy rejuvenates the mitochondrial–lysosomal axis and alleviates autophagic blockage in Pompe disease Academic Article
- Duvoglustat HCl Increases Systemic and Tissue Exposure of Active Acid α-Glucosidase in Pompe Patients Co-administered with Alglucosidase α Academic Article
- Enzyme replacement therapy for Anderson-Fabry disease: A complementary overview of a Cochrane publication through a linear regression and a pooled analysis of proportions from cohort studies Academic Article
- Healthcare resource utilization in the management of hypophosphatasia in three patients displaying a spectrum of manifestations Academic Article
- Hypophosphatasia: Canadian update on diagnosis and management Academic Article
- Safety and efficacy of avalglucosidase alfa versus alglucosidase alfa in patients with late-onset Pompe disease (COMET): a phase 3, randomised, multicentre trial Academic Article
- Safety and physiological effects of two different doses of elosulfase alfa in patients with morquio a syndrome: A randomized, double-blind, pilot study Academic Article