Načítá se...
Enzyme therapy and immune response in relation to CRIM status: the Dutch experience in classic infantile Pompe disease
BACKGROUND: Enzyme-replacement therapy (ERT) in Pompe disease—an inherited metabolic disorder caused by acid α-glucosidase deficiency and characterized in infants by generalized muscle weakness and cardiomyopathy—can be complicated by immune responses. Infants that do not produce any endogenous acid...
Uloženo v:
| Vydáno v: | J Inherit Metab Dis |
|---|---|
| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Springer Netherlands
2014
|
| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4341007/ https://ncbi.nlm.nih.gov/pubmed/24715333 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10545-014-9707-6 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|