Use of Cardiac Magnetic Resonance Imaging to Evaluate Cardiac Structure, Function and Fibrosis in Children with Infantile Pompe Disease on Enzyme Replacement Therapy

BACKGROUND: Pompe disease (acid α-glucosidase deficiency) is one of several lysosomal storage diseases amenable to treatment with enzyme replacement therapy (ERT). While echocardiography (echo) has been the standard method to evaluate the cardiac response to ERT, cardiac magnetic resonance imaging (...

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Hauptverfasser: Barker, Piers C.A., Pasquali, Sara K., Darty, Stephen, Ing, Richard J., Li, Jennifer S., Kim, Raymond J., DeArmey, Stephanie, Kishnani, Priya S., Campbell, Michael J.
Format: Artigo
Sprache:Inglês
Veröffentlicht: 2010
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Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2991632/
https://ncbi.nlm.nih.gov/pubmed/20875764
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2010.07.011
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