Hyperpolarized 13C probe development has allowed in vivo monitoring of different physiological processes relating to various diseases, including cancer and diabetes. Each new probe is typically characterized with polarization and T1 measurements, but T2 is also an important parameter for optimal sequence design, including progressive flip angle schemes. To improve the spatiotemporal resolution of T2 mapping sequences and subsequent multi-exponential analysis, this project investigated using a local low rank plus sparse reconstruction for 2-fold acceleration of in vivo T2 mapping with the bSSFP sequence.
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