The utilization of magnetic resonance (MR) im-aging to guide near-infrared spectral tomography (NIRST) shows significant potential for improving the specificity and sensitivity of breast cancer diagnosis. However, the ef-ficiency and accuracy of NIRST image reconstruction have been limited by the complexities of light propagation mod-eling and MRI image segmentation. To address these chal-lenges, we developed and evaluated a deep learning-based approach for MR-guided 3D NIRST image reconstruction (DL-MRg-NIRST). Using a network trained on synthetic data, the DL-MRg-NIRST system reconstructed images from data acquired during 38 clinical imaging exams of pa-tients with breast abnormalities. Statistical analysis of the results demonstrated a sensitivity of 87.5%, a specificity of 92.9%, and a diagnostic accuracy of 89.5% in distinguishing pathologically defined benign from malignant lesions. Ad-ditionally, the combined use of MRI and DL-MRg-NIRST di-agnoses achieved an area under the receiver operating characteristic (ROC) curve of 0.98. Remarkably, the DL-MRg-NIRST image reconstruction process required only 1.4 seconds, significantly faster than state-of-the-art MR-guided NIRST methods.

To investigate vessel delineation and image quality of ultra-high-resolution (UHR) CT angiography (CTA) reconstructed using deep learning reconstruction (DLR) optimised for brain CTA (DLR-brain) in moyamoya disease (MMD), compared with DLR optimised for body CT (DLR-body) and hybrid iterative reconstruction (Hybrid-IR). This retrospective study included 50 patients with suspected or diagnosed MMD who underwent UHR brain CTA. All images were reconstructed using DLR-brain, DLR-body, and Hybrid-IR. Quantitative analysis focussed on moyamoya perforator vessels in the basal ganglia and periventricular anastomosis. For these small vessels, edge sharpness, peak CT number, vessel contrast, full width at half maximum (FWHM), and image noise were measured and compared. Qualitative analysis was performed by visual assessment to compare vessel delineation and image quality. DLR-brain significantly improved edge sharpness, peak CT number, vessel contrast, and FWHM, and significantly reduced image noise compared with DLR-body and Hybrid-IR (P < 0.05). DLR-brain significantly outperformed the other algorithms in the visual assessment (P < 0.001). DLR-brain provided superior visualisation of small intracranial vessels compared with DLR-body and Hybrid-IR in UHR brain CTA.

We propose a self-supervised feature learning assisted reconstruction (SSFL-Recon) framework for MRI reconstruction to address the limitation of existing supervised learning methods. Although recent deep learning-based methods have shown promising performance in MRI reconstruction, most require fully-sampled images for supervised learning, which is challenging in practice considering long acquisition times under respiratory or organ motion. Moreover, nearly all fully-sampled datasets are obtained from conventional reconstruction of mildly accelerated datasets, thus potentially biasing the achievable performance. The numerous undersampled datasets with different accelerations in clinical practice, hence, remain underutilized. To address these issues, we first train a self-supervised feature extractor on undersampled images to learn sampling-insensitive features. The pre-learned features are subsequently embedded in the self-supervised reconstruction network to assist in removing artifacts. Experiments were conducted retrospectively on an in-house 2D cardiac Cine dataset, including 91 cardiovascular patients and 38 healthy subjects. The results demonstrate that the proposed SSFL-Recon framework outperforms existing self-supervised MRI reconstruction methods and even exhibits comparable or better performance to supervised learning up to $16\times$ retrospective undersampling. The feature learning strategy can effectively extract global representations, which have proven beneficial in removing artifacts and increasing generalization ability during reconstruction.

Cardiovascular magnetic resonance (CMR) cine imaging is the gold standard for assessing ventricular volumes and function. It typically requires two-dimensional (2D) bSSFP sequences and multiple breath-holds, which can be challenging for patients with limited breath-holding capacity. Three-dimensional (3D) cardiovascular magnetic resonance angiography (MRA) usually suffers from lengthy acquisition. Free-running 3D cine imaging with deep learning (DL) reconstruction offers a potential solution by acquiring both cine and angiography simultaneously. To evaluate the efficiency and accuracy of a ferumoxytol-enhanced 3D cine imaging MR sequence combined with DL reconstruction and Heart-NAV technology in patients with congenital heart disease. This Institutional Review Board approved this prospective study that compared (i) functional and volumetric measurements between 3 and 2D cine images; (ii) contrast-to-noise ratio (CNR) between deep-learning (DL) and compressed sensing (CS)-reconstructed 3D cine images; and (iii) cross-sectional area (CSA) measurements between DL-reconstructed 3D cine images and the clinical 3D MRA images acquired using the bSSFP sequence. Paired t-tests were used to compare group measurements, and Bland-Altman analysis assessed agreement in CSA and volumetric data. Sixteen patients (seven males; median age 6 years) were recruited. 3D cine imaging showed slightly larger right ventricular (RV) volumes and lower RV ejection fraction (EF) compared to 2D cine, with a significant difference only in RV end-systolic volume (P = 0.02). Left ventricular (LV) volumes and EF were slightly higher, and LV mass was lower, without significant differences (P ≥ 0.05). DL-reconstructed 3D cine images showed significantly higher CNR in all pulmonary veins than CS-reconstructed 3D cine images (all P < 0.05). Highly accelerated free-running 3D cine imaging with DL reconstruction shortens acquisition times and provides comparable volumetric measurements to 2D cine, and comparable CSA to clinical 3D MRA.

Low-dose computed tomography (LDCT) effectively reduces radiation exposure to patients, but introduces severe noise artifacts that affect diagnostic accuracy. Recently, Transformer-based network architectures have been widely applied to LDCT image denoising, generally achieving superior results compared to traditional convolutional methods. However, these methods are often hindered by high computational costs and struggles in capturing complex local contextual features, which negatively impact denoising performance. In this work, we propose CT-Denoimer, an efficient CT Denoising Transformer network that captures both global correlations and intricate, spatially varying local contextual details in CT images, enabling the generation of high-quality images. The core of our framework is a Transformer module that consists of two key components: the Multi-Dconv head Transposed Attention (MDTA) and the Mixed Contextual Feed-forward Network (MCFN). The MDTA block captures global correlations in the image with linear computational complexity, while the MCFN block manages multi-scale local contextual information, both static and dynamic, through a series of Enhanced Contextual Transformer (eCoT) modules. In addition, we incorporate Operation-Wise Attention Layers (OWALs) to enable collaborative refinement in the proposed CT-Denoimer, enhancing its ability to more effectively handle complex and varying noise patterns in LDCT images. Extensive experimental validation on both the AAPM-Mayo public dataset and a real-world clinical dataset demonstrated the state-of-the-art performance of the proposed CT-Denoimer. It achieved a peak signal-to-noise ratio (PSNR) of 33.681 dB, a structural similarity index measure (SSIM) of 0.921, an information fidelity criterion (IFC) of 2.857 and a visual information fidelity (VIF) of 0.349. Subjective assessment by radiologists gave an average score of 4.39, confirming its clinical applicability and clear advantages over existing methods. This study presents an innovative CT denoising Transformer network that sets a new benchmark in LDCT image denoising, excelling in both noise reduction and fine structure preservation.

Dynamic Photoacoustic Computed Tomography (PACT) is an important imaging technique for monitoring physiological processes, capable of providing high-contrast images of optical absorption at much greater depths than traditional optical imaging methods. However, practical instrumentation and geometric constraints limit the number of acoustic sensors available around the imaging target, leading to sparsity in sensor data. Traditional photoacoustic (PA) image reconstruction methods, when directly applied to sparse PA data, produce severe artifacts. Additionally, these traditional methods do not consider the inter-frame relationships in dynamic imaging. Temporal resolution is crucial for dynamic photoacoustic imaging, which is fundamentally limited by the low repetition rate (e.g., 20 Hz) and high cost of high-power laser technology. Recently, Implicit Neural Representation (INR) has emerged as a powerful deep learning tool for solving inverse problems with sparse data, by characterizing signal properties as continuous functions of their coordinates in an unsupervised manner. In this work, we propose an INR-based method to improve dynamic photoacoustic image reconstruction from sparse-views and enhance temporal resolution, using only spatiotemporal coordinates as input. Specifically, the proposed INR represents dynamic photoacoustic images as implicit functions and encodes them into a neural network. The weights of the network are learned solely from the acquired sparse sensor data, without the need for external training datasets or prior images. Benefiting from the strong implicit continuity regularization provided by INR, as well as explicit regularization for low-rank and sparsity, our proposed method outperforms traditional reconstruction methods under two different sparsity conditions, effectively suppressing artifacts and ensuring image quality.

Dynamic magnetic resonance imaging (MRI) plays an indispensable role in cardiac diagnosis. To enable fast imaging, the k-space data can be undersampled but the image reconstruction poses a great challenge of high-dimensional processing. This challenge necessitates extensive training data in deep learning reconstruction methods. In this work, we propose a novel and efficient approach, leveraging a dimension-reduced separable learning scheme that can perform exceptionally well even with highly limited training data. We design this new approach by incorporating spatiotemporal priors into the development of a Deep Separable Spatiotemporal Learning network (DeepSSL), which unrolls an iteration process of a 2D spatiotemporal reconstruction model with both temporal lowrankness and spatial sparsity. Intermediate outputs can also be visualized to provide insights into the network behavior and enhance interpretability. Extensive results on cardiac cine datasets demonstrate that the proposed DeepSSL surpasses stateof-the-art methods both visually and quantitatively, while reducing the demand for training cases by up to 75%. Additionally, its preliminary adaptability to unseen cardiac patients has been verified through a blind reader study conducted by experienced radiologists and cardiologists. Furthermore, DeepSSL enhances the accuracy of the downstream task of cardiac segmentation and exhibits robustness in prospectively undersampled real-time cardiac MRI. DeepSSL is efficient under highly limited training data and adaptive to patients and prospective undersampling. This approach holds promise in addressing the escalating demand for high-dimensional data reconstruction in MRI applications.

Three-dimensional ultrasound enables real-time volumetric visualization of anatomical structures. Unlike traditional 2D ultrasound, 3D imaging reduces the reliance on precise probe orientation, potentially making ultrasound more accessible to clinicians with varying levels of experience and improving automated measurements and post-exam analysis. However, achieving both high volume rates and high image quality remains a significant challenge. While 3D diverging waves can provide high volume rates, they suffer from limited tissue harmonic generation and increased multipath effects, which degrade image quality. One compromise is to retain the focusing in elevation while leveraging unfocused diverging waves in the lateral direction to reduce the number of transmissions per elevation plane. Reaching the volume rates achieved by full 3D diverging waves, however, requires dramatically undersampling the number of elevation planes. Subsequently, to render the full volume, simple interpolation techniques are applied. This paper introduces a novel approach to 3D ultrasound reconstruction from a reduced set of elevation planes by employing diffusion models (DMs) to achieve increased spatial and temporal resolution. We compare both traditional and supervised deep learning-based interpolation methods on a 3D cardiac ultrasound dataset. Our results show that DM-based reconstruction consistently outperforms the baselines in image quality and downstream task performance. Additionally, we accelerate inference by leveraging the temporal consistency inherent to ultrasound sequences. Finally, we explore the robustness of the proposed method by exploiting the probabilistic nature of diffusion posterior sampling to quantify reconstruction uncertainty and demonstrate improved recall on out-of-distribution data with synthetic anomalies under strong subsampling.

Dynamic MRI plays a vital role in clinical practice by capturing both spatial details and dynamic motion, but its high spatiotemporal resolution is often limited by long scan times. Deep learning (DL)-based methods have shown promising performance in accelerating dynamic MRI. However, most existing algorithms rely on large fully-sampled datasets for training, which are difficult to acquire. Recently, implicit neural representation (INR) has emerged as a powerful scan-specific paradigm for accelerated MRI, which models signals as a continuous function over spatiotemporal coordinates. Although this approach achieves efficient continuous modeling of dynamic images and robust reconstruction, it faces challenges in recovering fine details and increasing computational demands for high dimensional data representation. To enhance both efficiency and reconstruction quality, we propose TenF-INR, a novel patch-based unsupervised framework that employs INR to model bases of tensor decomposition, enabling efficient and accurate modeling of dynamic MR images with learnable tensor functions. By exploiting strong correlations in similar spatial image patches and in the temporal direction, TenF-INR enforces multidimensional low-rankness and implements patch-based reconstruction with the benefits of continuous modeling. We compare TenF-INR with state-of-the-art methods, including supervised DL methods and unsupervised approaches. Experimental results demonstrate that TenF-INR achieves high acceleration factors up to 21, outperforming all comparison methods in image quality, temporal fidelity, and quantitative metrics, even surpassing the supervised methods.

Chemical Exchange Saturation Transfer (CEST) MRI has demonstrated its remarkable ability to enhance the detection of macromolecules and metabolites with low concentrations. While CEST mapping is essential for quantifying molecular information, conventional methods face critical limitations: model-based approaches are constrained by limited sensitivity and robustness depending heavily on parameter setups, while data-driven deep learning methods lack generalizability across heterogeneous datasets and acquisition protocols. To overcome these challenges, we propose a Lorentzian-model Informed Neural Representation (LINR) framework for high-quality CEST mapping. LINR employs a self-supervised neural architecture embedding the Lorentzian equation - the fundamental biophysical model of CEST signal evolution - to directly reconstruct high-sensitivity parameter maps from raw z-spectra, eliminating dependency on labeled training data. Convergence of the self-supervised training strategy is guaranteed theoretically, ensuring LINR's mathematical validity. The superior performance of LINR in capturing CEST contrasts is revealed through comprehensive evaluations based on synthetic phantoms and in-vivo experiments (including tumor and Alzheimer's disease models). The intuitive parameter-free design enables adaptive integration into diverse CEST imaging workflows, positioning LINR as a versatile tool for non-invasive molecular diagnostics and pathophysiological discovery.