Purpose To develop an efficient acquisition for high‐resolution diffusion imaging and allow in vivo whole‐brain acquisitions at 600‐ to 700‐μm isotropic resolution. Methods We combine blipped‐controlled aliasing in parallel imaging simultaneous multislice (SMS) with a novel slab radiofrequency (RF) encoding gSlider (generalized slice‐dithered enhanced resolution) to form a signal‐to‐noise ratio–efficient volumetric simultaneous multislab acquisition. Here, multiple thin slabs are acquired simultaneously with controlled aliasing, and unaliased with parallel imaging. To achieve high resolution in the slice direction, the slab is volumetrically encoded using RF encoding with a scheme similar to Hadamard encoding. However, with gSlider, the RF‐encoding bases are specifically designed to be highly independent and provide high image signal‐to‐noise ratio in each slab acquisition to enable self‐navigation of the diffusion's phase corruption. Finally, the method is combined with zoomed imaging (while retaining whole‐brain coverage) to facilitate low‐distortion single‐shot in‐plane encoding with echo‐planar imaging at high resolution. Results A 10‐slices‐per‐shot gSlider‐SMS acquisition was used to acquire whole‐brain data at 660 and 760 μm isotropic resolution with b‐values of 1500 and 1800 s/mm2, respectively. Data were acquired on the Connectome 3 Tesla scanner with 64‐channel head coil. High‐quality data with excellent contrast were achieved at these resolutions, which enable the visualization of fine‐scale structures. Conclusions The gSlider‐SMS approach provides a new, efficient way to acquire high‐resolution diffusion data. Magn Reson Med 79:141–151, 2018. © 2017 International Society for Magnetic Resonance in Medicine.

Purpose To develop an efficient distortion‐ and blurring‐free multi‐shot EPI technique for time‐resolved multiple‐contrast and/or quantitative imaging. Methods EPI is a commonly used sequence but suffers from geometric distortions and blurring. Here, we introduce a new multi‐shot EPI technique termed echo planar time‐resolved imaging (EPTI), which has the ability to rapidly acquire distortion‐ and blurring‐free multi‐contrast data set. The EPTI approach performs encoding in ky‐t space and uses a new highly accelerated spatio–temporal CAIPI sampling trajectory to take advantage of signal correlation along these dimensions. Through this acquisition and a B0‐informed parallel imaging reconstruction, hundreds of “time‐resolved” distortion‐ and blurring‐free images at different TEs across the EPI readout window can be created at sub‐millisecond temporal increments using a small number of EPTI shots. Moreover, a method for self‐estimation and correction of shot‐to‐shot B0 variations was developed. Simultaneous multi‐slice acquisition was also incorporated to further improve the acquisition efficiency. Results We evaluated EPTI under varying simulated acceleration factors, B0‐inhomogeneity, and shot‐to‐shot B0 variations to demonstrate its ability to provide distortion‐ and blurring‐free images at multiple TEs. Two variants of EPTI were demonstrated in vivo at 3T: (1) a combined gradient‐ and spin‐echo EPTI for quantitative mapping of T2, T2*, proton density, and susceptibility at 1.1 × 1.1 × 3 mm3 whole‐brain in 28 s (0.8 s/slice), and (2) a gradient‐echo EPTI, for multi‐echo and quantitative T2* fMRI at 2 × 2 × 3 mm3 whole‐brain at a 3.3 s temporal resolution. Conclusion EPTI is a new approach for multi‐contrast and/or quantitative imaging that can provide fast acquisition of distortion‐ and blurring‐free images at multiple TEs.