T1 mapping of the fetal brain is hindered by substantial, frequent, and random fetal motion, making many current quantitative techniques impractical in the fetus. We have applied to the fetal brain (and adult brain for validation purposes) a recently introduced T1 mapping technique based on EPI readout that is preceded by a non-selective inversion pulse, and where the order of the acquired slices is permuted from one inversion recovery to the next, allowing efficient, high temporal sampling of the T1 relaxation curve. We believe that this method is capable of providing accurate T1 maps of the fetal brain.
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