Purpose: Electrocardiogram (ECG) abnormalities are universal in infantile Pompe disease or glycogen storage disease type II, a fatal genetic muscle disorder caused by deficiency of acid α-glucosidase ...

In a previous 52-wk trial, treatment with alglucosidase alfa markedly improved cardiomyopathy, ventilatory function, and overall survival among 18 children <7 mo old with infantile-onset Pompe disease ...

ProSys announces acquisition to complement existing filling lines and to grow common market shares. Webb City, MO (Jan. 9, 2025) — ProSys Fill LLC. today announced the purchase of Pendergraph Machines ...

Majority ownership of ProSys enables tighter integration of specialized sampling and isolation equipment within a global machinery platform, potentially improving access to high-integrity aseptic and ...

This content was written and submitted by the supplier. It has only been modified to comply with this publication’s space and style. The IMA Group strengthens its presence in aseptic and containment ...

Interim biomarker data from the first 4 patients showed lower creatine kinase levels by week 10, with 3 of the 4 also showing Glc4 reductions. Aro Biotherapeutics announced positive interim results ...

horreur•Le propriétaire d’une maison funéraire « écolo » a été condamné à 40 ans de prison pour avoir escroqué des centaines de familles et dissimulé les cadavres des défunts ...