Quantitative Magnetic Resonance Imaging (MRI) is based on a two-steps approach: estimation of the magnetic moments distribution inside the body, followed by a voxel-by-voxel quantification of the human tissue properties. This splitting simplifies the computations but poses several constraints on the measurement process, limiting its efficiency. Here, we perform quantitative MRI as a one step process; signal localization and parameter quantification are simultaneously obtained by the solution of a large scale nonlinear inversion problem based on first-principles. As a consequence, the constraints on the measurement process can be relaxed and acquisition schemes that are time efficient and widely available in clinical MRI scanners can be employed. We show that the nonlinear tomography approach is applicable to MRI and returns human tissue maps from very short experiments.
Magnetic resonance fingerprinting (MRF) is able to estimate multiple quantitative tissue parameters from a relatively short acquisition. The main characteristic of an MRF sequence is the simultaneous application of (a) transient states excitation and (b) highly undersampled k-space. Despite the promising empirical results obtained with MRF, no work has appeared that formally describes the combined impact of these two aspects on the reconstruction accuracy. In this paper, a mathematical model is derived that directly relates the time varying RF excitation and the k-space sampling to the spatially dependent reconstruction errors. A subsequent in-depth analysis identifies the mechanisms by which MRF sequence properties affect accuracy, providing a formal explanation of several empirically observed or intuitively understood facts. New insights are obtained which show how this analytical framework could be used to improve the MRF protocol.
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