Is this you? As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work.
Claim your profile
Get in touch with Carolina Teles
Contact Carolina Teles, search articles and posts on X, monitor coverage, and track replies from one place.
Learn more about Muck RackActions
Is this you?
As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work.Articles
Untargeted Lipidomics in Fabry Disease of Urine Samples by Low-Resolution Flow Injection Mass Spectrometry (ESI(±)-LTQ MS)
1. Introduction Click to copy section linkSection link copied! Fabry disease (FD) is an X-linked lysosomal storage disease caused by a mutation in the gene encoding the enzyme α-galactosidase A (α-GAL A). (1) A reduction or absence of α-GAL A activity results in the progressive accumulation of the substrates globotriaosylceramide (Gb3), globotriaosylsphingosine (lyso-Gb3), and related glycosphingolipids in various cell types, affecting multiple systems and afflicting both males and females.
Actions
Is this you?
As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work.Get in touch with Carolina Teles
Contact Carolina Teles, search articles and posts on X, monitor coverage, and track replies from one place.
Learn more about Muck Rack