Cape Town - 2026 ISMRM-ISMRT Annual Meeting and Exhibition • 09-14 May 2026
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567-04-001.
Comparing accelerated encoding strategies for Multi-echo Gradient Echo Quantitative Imaging free of physiological artifacts
Impact: We aim to test acceleration and
physiological noise (cardiac and respiratory) mitigation strategies in an open
source multi-echo GRE sequence geared towards R2* mapping, Quantitative
Susceptibility Mapping (QSM) and Multi-compartment Relaxometry Myelin Water
Imaging (MWI), using conventional 3T clinical hardware.
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567-04-002.
White Matter Damage in Temporal Lobe Epilepsy with Hippocampal Sclerosis: A NODDI and Automated Segmentation Study
Impact: This study’s findings on WM volume reductions and NODDI metric
alterations in TLE-HS patients can enhance surgical planning and prognosis,
guiding clinicians in targeting epileptogenic regions more precisely and
potentially improving patient outcomes.
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567-04-003.
Progressive Reorganization of Cortical Functional Connectivity Gradients in Non-Dialysis Patients With Chronic Kidney Disease
Impact: This study reveals early-onset hierarchical brain disruptions in CKD and their progressive aggravation with renal decline, providing insights into dynamic kidney–brain interactions and enabling stage-specific evaluation of cognitive vulnerability in non-dialysis patients.
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567-04-004.
Clinical head MR images in Finnish MR sites
Impact: Analysis of
clinical image quality done in a large setting in this study, gives insight
into practices that provide better images. This can potentially lead to better
clinical image quality on a national level, which undoubtedly improves patient
care.
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567-04-005.
Selective Vulnerability of Left Fimbria in Cognitively Normal APOE ε4 Carriers: A Neuroimaging Signature of Preclinical AD
Impact: This study indicate that the left fimbria may serve as a neuroimaging structure of preclinical Alzheimer's disease, offering insights into gene-brain-cognition pathways and informing strategies for early risk stratification and intervention in individuals at genetic risk for AD.
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567-04-006.
Rapid multiparametric quantitative MRI for predicting the activity of thyroid-associated ophthalmopathy
Impact: Active and inactive TAO are differently treated in clinic. Accurately discriminating active from inactive TAO is important for treatment selection. Our study suggested the application of multiparametric quantitative MRI would be beneficial for guiding TAO treatment selection in clinical practice.
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567-04-007.
MRI-Based Prediction of Ischemic Stroke in Patients with Internal Carotid Artery Occlusion
Impact: MRI-based
Cox risk stratification flags high-risk ICAO patients early, prioritizing
follow-up, intensifying antithrombotic therapy, and guiding revascularization.
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567-04-008.
The changes in the gray matter volume of the thalamus, hippocampus and amygdala in classic trigeminal neuralgia.
Impact: Previous studies on the
subregions of the thalamus, amygdala and hippocampus of CTN disease have been
relatively scarce. The findings of this study are expected to provide a new
direction for the exploration of clinical therapeutic targets.
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567-04-009.
High-resolution perfusion imaging of the human cerebral cortex with high-performance MRI
Impact: Noninvasive
perfusion imaging approaches with high-spatial resolution could help improve
our understanding of cortical hemodynamic physiology at the laminar level,
including how these effects may evolve in the aging brain.
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567-04-010.
Olfactory and Neurochemical Alterations Underlying Craving and Reward Dysregulation in Alcohol Use Disorder
Impact: Identifying olfactory and neurochemical biomarkers of craving can guide
personalized, odor-based, non-invasive interventions to reduce relapse risk and
improve emotional regulation in Alcohol Use Disorder.
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567-04-011.
Bundle-Resolved Orientation Dependence of White Matter T1 via Controlled Head Reorientation
Impact: Demonstrating tract‑resolved angle effects on T1,
provides references that help avoid misreading regional differences, and guide
more consistent longitudinal interpretation, enabling more reliable application
of T1 in clinical white‑matter tracts.
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