To the Editor: We read with interest the article titled “Cardiovascular Abnormalities in Late Onset Pompe Disease and ERT” by Forsha et al. 1. Ninety patients were randomized 2:1 to enzyme replacement ...
Fabry's disease is a rare, X-linked disorder characterized by subnormal or absent activity of the lysosomal hydrolase α-galactosidase A. A deficiency of α-galactosidase A leads to progressive ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results