Ability to form Sox17-induced hematopoietic cell clusters varies among distinct hematopoietic sites during development. [PDF]
Itabashi A +8 more
europepmc +1 more source
Olipudase alfa IgE-mediated anaphylaxis prevented by omalizumab and tailored desensitization in a child with acid sphingomyelinase deficiency. [PDF]
Fiori L +6 more
europepmc +1 more source
Pompe Disease: Pathogenesis, Molecular Mechanisms, Neurological Aspects, Diagnostics and Modern Therapeutic Approaches. [PDF]
Sharshakova A +6 more
europepmc +1 more source
Assessment of bone health and bone mineral density in patients with mucopolysaccharidosis receiving enzyme replacement therapy. [PDF]
El Feil NSA, Abuzaid Y, Mobarak A.
europepmc +1 more source
Improvement in quality of life and general functions in pediatric acid sphingomyelinase deficiency patients after receiving olipudase alfa: A single-center experience in Taiwan. [PDF]
Pan YW, Yu WH, Tsai MC, Chou YY.
europepmc +1 more source
Seawater intrusion assessment in sandbar aquifer based on numerical modeling and electrical resistivity tomography, southern Baltic coast, Poland. [PDF]
Jaworska-Szulc B +6 more
europepmc +1 more source
TRPML1 agonists synergize with enzyme replacement therapy in fibroblasts from Pompe disease patients. [PDF]
Damiano C +10 more
europepmc +1 more source
Comparing the efficacy of cipaglucosidase alfa plus miglustat with alglucosidase alfa for late-onset Pompe disease: an expanded network meta-analysis utilizing patient-level and aggregate data. [PDF]
Fu S +8 more
europepmc +1 more source
Sex-based antibody subclass maturation drives direct enzymatic inhibition in fabry disease patients receiving enzyme replacement therapy. [PDF]
Baldwin T +18 more
europepmc +1 more source

