The atherogenic mechanism of homocystinemia has been defined by measuring endothelial
cell loss and regeneration, platelet consumption, and intimal lesion formation in a primate …

… Nineteen survival and turnover measurements of 51 Cr-platelets, 131 I-fibrinogen and 125
I-plasminogen in four homocystinuric patients demonstrated uniformly a threefold increase in …

… Given the relationships between activity and communication theorized by Corman and Scott
(1994), we also have the theoretical tools to understand how acts of identification, shaping …

Gaucher disease (GD) is an autosomal recessive disorder caused by the deficiency of
glucocerebrosidase, a lysosomal enzyme that catalyses the hydrolysis of the glycolipid …

PURPOSE: Gaucher disease is the first lysosomal storage disorder to be treated with
macrophage-targeted enzyme replacement therapy. Previous studies in relatively small numbers of …

Background The Gaucher Registry, the largest database of patients with Gaucher disease (GD)
worldwide, was initiated to better delineate the progressive nature of the disorder and …

Bloggers are typically cautious about engaging in self-disclosure because of concerns that
what they post may have negative consequences. This article examines the relationship …

Background Fabry’s disease, an X-linked disorder of lysosomal α-galactosidase deficiency,
leads to substrate accumulation in multiple organs. Migalastat, an oral pharmacologic …

This book is mainly intended to meet the needs of undergraduate students of Civil Engineering.
A certain amount of factual information, in the form of design charts and tables, has been …

The Fabry Registry is a global observational research platform established to define outcome
data on the natural and treated course of this rare disorder. Participating physicians submit …