Quantitative magnetic resonance imaging (qMRI) has attracted more and more attention in clinical diagnosis and medical sciences due to its capability to non-invasively characterize tissue properties. Nevertheless, most qMRI methods are time-consuming and sensitive to motion, making them inadequate for quantifying organs with physiological movement. In this context, single-shot multiple overlapping-echo detachment (MOLED) imaging technique has been presented, but its acquisition efficiency and image quality are limited when the field of view (FOV) is smaller than the object, especially for abdominal organs and myocardium. A novel single-shot reduced FOV qMRI method was developed based on MOLED (termed rFOV-MOLED). This method combines zonal oblique multislice (ZOOM) and outer volume suppression (OVS) techniques to reduce the FOV and suppress signals outside the FOV. A deep neural network was trained using synthetic data generated from Bloch simulations to achieve high-quality T₂ map reconstruction from rFOV-MOLED iamges. Numerical simulation, water phantom and in vivo abdominal and myocardial imaging experiments were performed to evaluate the method. The coefficient of variation and repeatability index were used to evaluate the reproducibility. Multiple statistical analyses were utilized to evaluate the accuracy and significance of the method, including linear regression, Bland-Altman analysis, Wilcoxon signed-rank test, and Mann-Whitney U test, with the p-value significance level of 0.05. Experimental results show that rFOV-MOLED achieved excellent performance in reducing aliasing signals due to FOV reduction. It provided T₂ maps closely resembling the reference maps. Moreover, it gave finer tissue details than MOLED and was quite repeatable. rFOV-MOLED can ultrafast and stably provide accurate T2 maps for myocardium and specific abdominal organs with improved acquisition efficiency and image quality.

Reduced signal-to-noise ratio (SNR) in hyperpolarized ¹²⁹Xe MR images can affect accurate quantification for research and diagnostic evaluations. Thus, this study explores the application of supervised deep learning (DL) denoising, traditional (Trad) and Noise2Noise (N2N) and unsupervised Noise2void (N2V) approaches for ¹²⁹Xe MR imaging. The DL denoising frameworks were trained and tested on 952 ¹²⁹Xe MRI data sets (421 ventilation, 125 diffusion-weighted, and 406 gas-exchange acquisitions) from healthy subjects and participants with cardiopulmonary conditions and compared with the block matching 3D denoising technique. Evaluation involved mean signal, noise standard deviation (SD), SNR, and sharpness. Ventilation defect percentage (VDP), apparent diffusion coefficient (ADC), membrane uptake, red blood cell (RBC) transfer, and RBC:Membrane were also evaluated for ventilation, diffusion, and gas-exchange images, respectively. Denoising methods significantly reduced noise SDs and enhanced SNR (p < 0.05) across all imaging types. Traditional ventilation model (Trad_vent) improved sharpness in ventilation images but underestimated VDP (bias = -1.37%) relative to raw images, whereas N2N_vent overestimated VDP (bias = +1.88%). Block matching 3D and N2V_vent showed minimal VDP bias (≤ 0.35%). Denoising significantly reduced ADC mean and SD (p < 0.05, bias ≤ - 0.63 × 10^-2). The values of Trad_vent and N2N_vent increased mean membrane and RBC (p < 0.001) with no change in RBC:Membrane. Denoising also reduced SDs of all gas-exchange metrics (p < 0.01). Low SNR may impair the potential of ¹²⁹Xe MRI for clinical diagnosis and lung function assessment. The evaluation of supervised and unsupervised DL denoising methods enhanced ¹²⁹Xe imaging quality, offering promise for improved clinical interpretation and diagnosis.

Magnetic susceptibility differences at the heart-lung interface introduce B₀-field inhomogeneities that challenge cardiac MRI at high field strengths (≥ 3 T). Although hardware-based shimming has advanced, conventional approaches often neglect dynamic variations in thoracic anatomy caused by cardiac and respiratory motion, leading to residual off-resonance artifacts. This study aims to characterize motion-induced B₀-field fluctuations in the heart and evaluate a deep learning-enabled motion-adaptive B₀ shimming pipeline to mitigate them. A motion-resolved B₀ mapping sequence was implemented at 3 T to quantify cardiac and respiratory-induced B₀ variations. A motion-adaptive shimming framework was then developed and validated through numerical simulations and human imaging studies. B₀-field homogeneity and T₂* mapping accuracy were assessed in multiple breath-hold positions using standard and motion-adaptive shimming. Respiratory motion significantly altered myocardial B₀ fields (p < 0.01), whereas cardiac motion had minimal impact (p = 0.49). Compared with conventional scanner shimming, motion-adaptive B₀ shimming yielded significantly improved field uniformity across both inspiratory (post-shim SD_ratio: 0.68 ± 0.10 vs. 0.89 ± 0.11; p < 0.05) and expiratory (0.65 ± 0.16 vs. 0.84 ± 0.20; p < 0.05) breath-hold states. Corresponding improvements in myocardial T₂* map homogeneity were observed, with reduced coefficient of variation (0.44 ± 0.19 vs. 0.39 ± 0.22; 0.59 ± 0.30 vs. 0.46 ± 0.21; both p < 0.01). The proposed motion-adaptive B₀ shimming approach effectively compensates for respiration-induced B₀ fluctuations, enhancing field homogeneity and reducing off-resonance artifacts. This strategy improves the robustness and reproducibility of T₂* mapping, enabling more reliable high-field cardiac MRI.

Metal artifacts, caused by high-density metallic implants in computed tomography (CT) imaging, severely degrade image quality, complicating diagnosis and treatment planning. While existing deep learning algorithms have achieved notable success in Metal Artifact Reduction (MAR), they often struggle to suppress artifacts while preserving structural details. To address this challenge, we propose FIND-Net (Fourier-Integrated Network with Dictionary Kernels), a novel MAR framework that integrates frequency and spatial domain processing to achieve superior artifact suppression and structural preservation. FIND-Net incorporates Fast Fourier Convolution (FFC) layers and trainable Gaussian filtering, treating MAR as a hybrid task operating in both spatial and frequency domains. This approach enhances global contextual understanding and frequency selectivity, effectively reducing artifacts while maintaining anatomical structures. Experiments on synthetic datasets show that FIND-Net achieves statistically significant improvements over state-of-the-art MAR methods, with a 3.07% MAE reduction, 0.18% SSIM increase, and 0.90% PSNR improvement, confirming robustness across varying artifact complexities. Furthermore, evaluations on real-world clinical CT scans confirm FIND-Net's ability to minimize modifications to clean anatomical regions while effectively suppressing metal-induced distortions. These findings highlight FIND-Net's potential for advancing MAR performance, offering superior structural preservation and improved clinical applicability. Code is available at https://github.com/Farid-Tasharofi/FIND-Net

Sparse-view computed tomography (CT) reduces radiation exposure by subsampling projection views, but conventional reconstruction methods produce severe streak artifacts with undersampled data. While deep-learning-based methods enable single-step artifact suppression, they often produce over-smoothed results under significant sparsity. Though diffusion models improve reconstruction via iterative refinement and generative priors, they require hundreds of sampling steps and struggle with stability in highly sparse regimes. To tackle these concerns, we present the Cross-view Generalized Diffusion Model (CvG-Diff), which reformulates sparse-view CT reconstruction as a generalized diffusion process. Unlike existing diffusion approaches that rely on stochastic Gaussian degradation, CvG-Diff explicitly models image-domain artifacts caused by angular subsampling as a deterministic degradation operator, leveraging correlations across sparse-view CT at different sample rates. To address the inherent artifact propagation and inefficiency of sequential sampling in generalized diffusion model, we introduce two innovations: Error-Propagating Composite Training (EPCT), which facilitates identifying error-prone regions and suppresses propagated artifacts, and Semantic-Prioritized Dual-Phase Sampling (SPDPS), an adaptive strategy that prioritizes semantic correctness before detail refinement. Together, these innovations enable CvG-Diff to achieve high-quality reconstructions with minimal iterations, achieving 38.34 dB PSNR and 0.9518 SSIM for 18-view CT using only \textbf{10} steps on AAPM-LDCT dataset. Extensive experiments demonstrate the superiority of CvG-Diff over state-of-the-art sparse-view CT reconstruction methods. The code is available at https://github.com/xmed-lab/CvG-Diff.

Neuromodulation of the centromedian nucleus (CM) of the thalamus has shown promise in treating refractory epilepsy, particularly for idiopathic generalized epilepsy and Lennox-Gastaut syndrome. However, precise targeting of CM remains challenging. The combination of deep learning reconstruction (DLR) and fast gray matter acquisition T1 inversion recovery (FGATIR) offers potential improvements in visualization of CM for deep brain stimulation (DBS) targeting. The goal of the study was to evaluate the visualization of the putative CM on DLR-FGATIR and its alignment with atlas-defined CM boundaries, with the aim of facilitating direct targeting of CM for neuromodulation. This retrospective study included 12 patients with drug-resistant epilepsy treated with thalamic neuromodulation by using DLR-FGATIR for direct targeting. Postcontrast-T1-weighted MRI, DLR-FGATIR, and postoperative CT were coregistered and normalized into Montreal Neurological Institute (MNI) space and compared with the Morel histologic atlas. Contrast-to-noise ratios were measured between CM and neighboring nuclei. CM segmentations were compared between an experienced rater, a trainee rater, the Morel atlas, and the Thalamus Optimized Multi Atlas Segmentation (THOMAS) atlas (derived from expert segmentation of high-field MRI) by using the Sorenson-Dice coefficient (Dice score, a measure of overlap) and volume ratios. The number of electrode contacts within the Morel atlas CM was assessed. On DLR-FGATIR, CM was visible as an ovoid hypointensity in the intralaminar thalamus. Contrast-to-noise ratios were highest (<i>P</i> < .001) for the mediodorsal and medial pulvinar nuclei. Dice score with the Morel atlas CM was higher (median 0.49, interquartile range 0.40-0.58) for the experienced rater (<i>P</i> < .001) than the trainee rater (0.32, 0.19-0.46) and no different (<i>P</i> = .32) than the THOMAS atlas CM (0.56, 0.55-0.58). Both raters and the THOMAS atlas tended to under-segment the lateral portion of the Morel atlas CM, reflected by smaller segmentation volumes (<i>P</i> < .001). All electrodes targeting CM based on DLR-FGATIR traversed the Morel atlas CM. DLR-FGATIR permitted visualization and delineation of CM commensurate with a group atlas derived from high-field MRI. This technique provided reliable guidance for accurate electrode placement within CM, highlighting its potential use for direct targeting.

Low-dose CT (LDCT) protocols reduce radiation exposure but increase image noise, compromising diagnostic confidence. Diffusion-based generative models have shown promise for LDCT denoising by learning image priors and performing iterative refinement. In this work, we introduce AST-n, an accelerated inference framework that initiates reverse diffusion from intermediate noise levels, and integrate high-order ODE solvers within conditioned models to further reduce sampling steps. We evaluate two acceleration paradigms--AST-n sampling and standard scheduling with high-order solvers -- on the Low Dose CT Grand Challenge dataset, covering head, abdominal, and chest scans at 10-25 % of standard dose. Conditioned models using only 25 steps (AST-25) achieve peak signal-to-noise ratio (PSNR) above 38 dB and structural similarity index (SSIM) above 0.95, closely matching standard baselines while cutting inference time from ~16 seg to under 1 seg per slice. Unconditional sampling suffers substantial quality loss, underscoring the necessity of conditioning. We also assess DDIM inversion, which yields marginal PSNR gains at the cost of doubling inference time, limiting its clinical practicality. Our results demonstrate that AST-n with high-order samplers enables rapid LDCT reconstruction without significant loss of image fidelity, advancing the feasibility of diffusion-based methods in clinical workflows.

Ultrasound imaging systems rely on accurate point spread function (PSF) estimation to support advanced image quality enhancement techniques such as deconvolution and speckle reduction. Phase aberration, caused by sound speed inhomogeneity within biological tissue, is inevitable in ultrasound imaging. It distorts the PSF by increasing sidelobe level and introducing asymmetric amplitude, making PSF estimation under phase aberration highly challenging. In this work, we propose a deep learning framework for estimating phase-aberrated PSFs using U-Net and complex U-Net architectures, operating on RF and complex k-space data, respectively, with the latter demonstrating superior performance. Synthetic phase aberration data, generated using the near-field phase screen model, is employed to train the networks. We evaluate various loss functions and find that log-compressed B-mode perceptual loss achieves the best performance, accurately predicting both the mainlobe and near sidelobe regions of the PSF. Simulation results validate the effectiveness of our approach in estimating PSFs under varying levels of phase aberration. Furthermore, we demonstrate that more accurate PSF estimation improves performance in a downstream phase aberration correction task, highlighting the broader utility of the proposed method.

We present MInDI-3D (Medical Inversion by Direct Iteration in 3D), the first 3D conditional diffusion-based model for real-world sparse-view Cone Beam Computed Tomography (CBCT) artefact removal, aiming to reduce imaging radiation exposure. A key contribution is extending the "InDI" concept from 2D to a full 3D volumetric approach for medical images, implementing an iterative denoising process that refines the CBCT volume directly from sparse-view input. A further contribution is the generation of a large pseudo-CBCT dataset (16,182) from chest CT volumes of the CT-RATE public dataset to robustly train MInDI-3D. We performed a comprehensive evaluation, including quantitative metrics, scalability analysis, generalisation tests, and a clinical assessment by 11 clinicians. Our results show MInDI-3D's effectiveness, achieving a 12.96 (6.10) dB PSNR gain over uncorrected scans with only 50 projections on the CT-RATE pseudo-CBCT (independent real-world) test set and enabling an 8x reduction in imaging radiation exposure. We demonstrate its scalability by showing that performance improves with more training data. Importantly, MInDI-3D matches the performance of a 3D U-Net on real-world scans from 16 cancer patients across distortion and task-based metrics. It also generalises to new CBCT scanner geometries. Clinicians rated our model as sufficient for patient positioning across all anatomical sites and found it preserved lung tumour boundaries well.

Passive acoustic mapping (PAM) is a promising tool for monitoring acoustic cavitation activities in the applications of ultrasound therapy. Data-adaptive beamformers for PAM have better image quality compared with time exposure acoustics (TEA) algorithms. However, the computational cost of data-adaptive beamformers is considerably expensive. In this work, we develop a deep beamformer based on a generative adversarial network that can switch between different transducer arrays and reconstruct high-quality PAM images directly from radiofrequency ultrasound signals with low computational cost. The deep beamformer was trained on a dataset consisting of simulated and experimental cavitation signals of single and multiple microbubble clouds measured by different (linear and phased) arrays covering 1-15 MHz. We compared the performance of the deep beamformer to TEA and three different data-adaptive beamformers using simulated and experimental test dataset. Compared with TEA, the deep beamformer reduced the energy spread area by 27.3%-77.8% and improved the image signal-to-noise ratio by 13.9-25.1 dB on average for the different arrays in our data. Compared with the data-adaptive beamformers, the deep beamformer reduced the computational cost by three orders of magnitude achieving 10.5 ms image reconstruction speed in our data, while the image quality was as good as that of the data-adaptive beamformers. These results demonstrate the potential of the deep beamformer for high-resolution monitoring of microbubble cavitation activities for ultrasound therapy.