3d Cine Mri
3d Cine Mri - Related Videos
08:22
3D Cine Magnetic Resonance Imaging of Respiratory Motion in Mechanically Ventilated Mice and Rats
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Cited by 1 •
2025
The proposed setup allows controlled mechanical ventilation and Magnetic Resonance imaging of 3D thorax movement in mice and rats. We have used this setup to study the pathophysiology underlying mechanical ventilation-induced respiratory muscle dysfunction.
15:53
Utilizing 3D Printing Technology to Merge MRI with Histology: A Protocol for Brain Sectioning
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Cited by 33 •
2016
The overall goal of this protocol is to accurately align magnetic resonance imaging (MRI) image volumes with histology sections via the creation of customized 3D-printed brain holders and slicer boxes.
06:06
Optogenetic Functional MRI
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Cited by 15 •
2016
This protocol describes the steps and data analysis required to successfully perform optogenetic functional magnetic resonance imaging (ofMRI). ofMRI is a novel technique that combines high-field fMRI readout with optogenetic stimulation, allowing for cell type-specific mapping of functional neural circuits and their dynamics across the whole living brain.
06:21
In Vivo MRI Analysis of Cranial Nerve Morphology in a Patient with Inner Ear Disorder
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2025
Source: Flatz, W. H. et al. In Vivo Morphometric Analysis of Human Cranial Nerves Using Magnetic Resonance Imaging in Menière's Disease Ears and Normal Hearing Ears. J. Vis. Exp. (2018).This video demonstrates the use of MRI to analyze cranial nerve morphology in the ears of patients suffering from a chronic inner ear disorder. It outlines the steps for performing a high magnetic field MRI scan on the patient, reconstructing the high-resolution 3D cross-sectional images of the cranial nerves,...
10:26
A Multicenter MRI Protocol for the Evaluation and Quantification of Deep Vein Thrombosis
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Cited by 5 •
2015
The goal of this study is to use magnetic resonance venography with long-circulating gadolinium-based contrast agent and direct thrombus imaging for quantitative evaluation of DVT volume in a multicenter, clinical trial setting. Inter- and intra-observer variability assessments were conducted, and reproducibility of the protocol was determined.
FAQs
Electrocardiographic synchronization organizes repeatedly acquired volumetric data according to the cardiac cycle. Reconstruction then presents the heart as a sequence of time-resolved volumes, allowing changes in ventricular shape, myocardial motion, and valve position to be examined throughout contraction and relaxation. This timing is important because functional abnormalities may appear only during particular portions of the cycle.
The technique distinguishes anatomical regions through differences in magnetic signal between tissues. Those differences provide contrast within each reconstructed volume, helping separate cardiac structures while they move. Combined with repeated acquisition over the cardiac cycle, tissue contrast allows anatomical assessment and supports interpretation of dynamic features such as myocardial motion and valve behavior.
A three-dimensional acquisition captures moving anatomy throughout a volume rather than restricting assessment to selected two-dimensional views. This broader representation can show spatial relationships and motion across the heart more comprehensively when limited views are insufficient. Because the examination uses magnetic resonance rather than ionizing radiation, it also provides a non-ionizing approach for repeated structural and functional assessment.
Reconstructed cardiac-cycle images support measurement of ventricular volumes and ejection fraction, which describes the proportion of ventricular blood volume expelled during contraction. They also permit assessment of myocardial motion and valve dynamics. Together, these measurements connect cardiac structure with function and provide quantitative and motion-based information for evaluating the heart.
It is especially useful when clinicians need a comprehensive view of cardiac motion or when two-dimensional imaging does not adequately capture the relevant anatomy. The method can help characterize both congenital and acquired heart disease, while its volumetric and time-resolved information supports evaluation of ventricular performance, myocardial movement, and valve dynamics.
By combining three-dimensional anatomy with motion across the cardiac cycle, the examination supplies information relevant to diagnosis and treatment planning. Measurements such as ventricular volumes and ejection fraction can also be compared during longitudinal monitoring, while changes in myocardial motion or valve dynamics may provide additional functional context for tracking congenital or acquired disease.