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Huwart, L., Sempoux, C., Salameh, N., Jamart, J., Annet, L., Sinkus, R., Peeters, F., terBeek, L.C., Horsmans, Y. and Van Beers, B.E. (2007) Liver Fibrosis: Noninvasive Assessment with MR Elastography Versus Aspartate Aminotransferase-to-Platelet Ratio Index. Radiology, 245, 458-466.
http://dx.doi.org/10.1148/radiol.2452061673

has been cited by the following article:

• TITLE: Dynamic Contrast-Enhanced MRI of Mouse Liver: A Feasibility Study Using a Dual-Input Two-Compartment Tracer Kinetic Model

  AUTHORS: Septian Hartono, Choon Hua Thng, Kai Hsiang Chuang, Huynh Hung, Tong San Koh

  KEYWORDS: DCE-MRI, Mouse, Liver Imaging, Preclinical Imaging

  JOURNAL NAME: Journal of Biomedical Science and Engineering, Vol.8 No.2, February 13, 2015

  ABSTRACT: Dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) has been widely applied to evaluate microcirculatory parameters in clinical settings. However, pre-clinical studies involving DCE-MRI of small animals remain challenging with the requirement for high spatial and temporal resolution for quantitative tracer kinetic analysis. This study illustrates the feasibility of applying a high temporal resolution (2 s) protocol for liver imaging in mice by analyzing the DCE-MRI datasets of mice liver with a dual-input two-compartment tracer kinetic model. Phantom studies were performed to validate the T1 estimates derived by the proposed protocol before applying it in mice studies. The DCE-MRI datasets of mice liver were amendable to tracer kinetic analysis using a dual-input two-compartment model. Estimated micro-circulatory parameters were consistent with liver physiology, indicating viability of applying the technique for pre-clinical drug developments.