(Circulation. 2008;118:109-112.)
© 2008 American Heart Association, Inc.
Editorial |
From the Cardiac MR Center, University Hospital Zurich and Childrens University Hospital, Zurich, Switzerland.
Correspondence to Juerg Schwitter, MD, FESC, University Hospital Zurich, Cardiology Clinics, Raemistrasse 100, CH-8091 Zurich, Switzerland. E-mail juerg.schwitter@usz.ch
Key Words: Editorials contrast media imaging magnetic resonance imaging metabolism spectroscopy
An extract of the first 250 words of the full text is provided, because this article has no abstract. |
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Article p 140
Flögel et al elegantly exploit a primary mode of action of inflammatory cells (ie, phagocytosis of potentially harmful agents), which in this case happens to be a magnetic resonance (MR)–active contrast medium. Another remarkable aspect of their work is the use of the naturally occurring stable fluorine isotope 19F as the MR-active nucleus for imaging. Why is this unique? This 19F-MR imaging strategy takes advantage of the fact that after administration of 19F-containing compounds, any signal detected in the body via MR imaging (MRI) is emanating from the injected contrast medium (ie, an extraordinary contrast-to-noise ratio [CNR] is present, because no background signal from the body is detected by 19F-MR imaging). If the MR scanner is thereafter tuned to the 1H resonance frequency, conventional MRI occurs, and all morphological and functional information on the organ
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