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Updated: May 13, 2026

Registered Bioimaging of Nanomaterials for Diagnostic and Therapeutic Monitoring
Published on: December 9, 2010
High-Accelerated Parallel Imaging With the Inherent Local Feature in PE-xSPEN MRI
Ke Dai1, Eddy Solomon2, Philip K Lee1
1National Engineering Research Center of Advanced Magnetic Resonance Technologies for Diagnosis and Therapy (NERC-AMRT), School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai, China.
Purpose:
To achieve highly accelerated high-resolution imaging with PE-xSPEN that efficiently utilizes the spatiotemporal encoded signals to physically distinguish contributions from distinct spatial locations prior to k-space acquisition, enabling the differentiation of aliased localized information in k-space.
Methods:
In the conventional k-space, undersampling along the phase-encoding dimension results in aliasing and overlapping replicas of the object along the spatial direction. The modulated hyperbolic phase arising from the PE-xSPEN encoding induces coupling between the and dimensions. So that for a given k-space location, the signal is predominantly contributed by local voxels. While undersampling along the PE dimension still causes aliased spatial replicas, these replicas remain distinguishable even without multi-channel coils after applying the traditional inverse Fourier transform along the undersampled dimension. Combining with parallel imaging, this approach enhances unfolding efficiency compared to traditional Fourier-encoded signals.
Results:
Combining with GRAPPA, the undersampled signals along the dimension can be reconstructed with fewer residual aliasing in PE-xSPEN compared to the traditional Fourier-encoded signals. The performance gain is demonstrated by MRI simulation, phantom tests, and in vivo brain experiments on 3T scanner.
Conclusion:
The proposed PE-xSPEN GRAPPA framework utilizes hyperbolic phase modulation to control aliasing artifacts and generate -dependent coil response, reducing artifacts and noise amplification.
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