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Result : Searchterm 'Image' found in 19 terms [] and 434 definitions []
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News  (255)  Resources  (73)  Forum  (128)  
 
Field Inhomogeneity ArtifactInfoSheet: - Artifacts - 
Case Studies, 
Reduction Index, 
etc.MRI Resource Directory:
 - Artifacts -
 
Quick Overview
Artifact Information
NAME
Field inhomogeneity
DESCRIPTION
Image distortion signal loss
REASON
HELP
Larger FOV, oversampling
A disturbance of the field homogeneity, because of magnetic material (inside or outside the patient), technical problems or scanning at the edge of the field.
When images were obtained in a progression from the center to the edge of the coil, the homogeneity of the field observed by the imaged volume, changes when the distance from the center of the volume increase. The same problem appears by scanning at a distance from the isocenter in left-right direction or too large field of view.
There are different types of bad image quality, the images are noisy, distorted or the fat suppression doesn't work because of badly set shim currents.
E.g. by using an IR sequence, changes in the T1 recovery rates of the tissues are involved. The inversion time at the center of the imaged volume is appropriate to suppress fat, but at the edge of the coil the same inversion time is sufficient to suppress water. Since the inversion time is not changed, the T1 recovery rates will increase.
mri safety guidance
Image Guidance
Take a smaller imaging volume (and for fat suppression a volume shimming), take care that the imaged region is at the center of the coil and that no magnetic material is inside the imaging volume.
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Further Reading:
  Basics:
MRI Artifact Gallery
   by chickscope.beckman.uiuc.edu    
MRI Resources 
Mobile MRI Rental - Intraoperative MRI - Jobs - Portals - Online Books - Pathology
 
Sensitivity EncodingInfoSheet: - Sequences - 
Intro, 
Overview, 
Types of, 
etc.
 
(SENSE) A MRI technique for relevant scan time reduction. The spatial information related to the coils of a receiver array are utilized for reducing conventional Fourier encoding. In principle, SENSE can be applied to any imaging sequence and k-space trajectories. However, it is particularly feasible for Cartesian sampling schemes. In 2D Fourier imaging with common Cartesian sampling of k-space sensitivity encoding by means of a receiver array enables to reduce the number of Fourier encoding steps.
SENSE reconstruction without artifacts relies on accurate knowledge of the individual coil sensitivities. For sensitivity assessment, low-resolution, fully Fourier-encoded reference images are required, obtained with each array element and with a body coil.
The major negative point of parallel imaging techniques is that they diminish SNR in proportion to the numbers of reduction factors. R is the factor by which the number of k-space samples is reduced. In standard Fourier imaging reducing the sampling density results in the reduction of the FOV, causing aliasing. In fact, SENSE reconstruction in the Cartesian case is efficiently performed by first creating one such aliased image for each array element using discrete Fourier transformation (DFT).
The next step then is to create a full-FOV image from the set of intermediate images. To achieve this one must undo the signal superposition underlying the fold-over effect. That is, for each pixel in the reduced FOV the signal contributions from a number of positions in the full FOV need to be separated. These positions form a Cartesian grid corresponding to the size of the reduced FOV.
The advantages are especially true for contrast-enhanced MR imaging such as dynamic liver MRI (liver imaging) , 3 dimensional magnetic resonance angiography (3D MRA), and magnetic resonance cholangiopancreaticography (MRCP).
The excellent scan speed of SENSE allows for acquisition of two separate sets of hepatic MR images within the time regarded as the hepatic arterial-phase (double arterial-phase technique) as well as that of multidetector CT.
SENSE can also increase the time efficiency of spatial signal encoding in 3D MRA. With SENSE, even ultrafast (sub second) 4D MRA can be realized.
For MRCP acquisition, high-resolution 3D MRCP images can be constantly provided by SENSE. This is because SENSE resolves the presence of the severe motion artifacts due to longer acquisition time. Longer acquisition time, which results in diminishing image quality, is the greatest problem for 3D MRCP imaging.
In addition, SENSE reduces the train of gradient echoes in combination with a faster k-space traversal per unit time, thereby dramatically improving the image quality of single shot echo planar imaging (i.e. T2 weighted, diffusion weighted imaging).
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• View the DATABASE results for 'Sensitivity Encoding' (12).Open this link in a new window

 
Further Reading:
  News & More:
Image Characteristics and Quality
   by www.sprawls.org    
MRI Resources 
Pathology - Calculation - Mobile MRI - Research Labs - Homepages - Claustrophobia
 
ContrastForum -
related threads
 
Contrast is the relative difference of signal intensities in two adjacent regions of an image.
Due to the T1 and T2 relaxation properties in magnetic resonance imaging, differentiation between various tissues in the body is possible. Tissue contrast is affected by not only the T1 and T2 values of specific tissues, but also the differences in the magnetic field strength, temperature changes, and many other factors. Good tissue contrast relies on optimal selection of appropriate pulse sequences (spin echo, inversion recovery, gradient echo, turbo sequences and slice profile).
Important pulse sequence parameters are TR (repetition time), TE (time to echo or echo time), TI (time for inversion or inversion time) and flip angle. They are associated with such parameters as proton density and T1 or T2 relaxation times. The values of these parameters are influenced differently by different tissues and by healthy and diseased sections of the same tissue.
For the T1 weighting it is important to select a correct TR or TI. T2 weighted images depend on a correct choice of the TE. Tissues vary in their T1 and T2 times, which are manipulated in MRI by selection of TR, TI, and TE, respectively. Flip angles mainly affect the strength of the signal measured, but also affect the TR/TI/TE parameters.
Conditions necessary to produce different weighted images:
T1 Weighted Image: TR value equal or less than the tissue specific T1 time - TE value less than the tissue specific T2 time.
T2 Weighted Image: TR value much greater than the tissue specific T1 time - TE value greater or equal than the tissue specific T2 time.
Proton Density Weighted Image: TR value much greater than the tissue specific T1 time - TE value less than the tissue specific T2 time.

See also Image Contrast Characteristics, Contrast Reversal, Contrast Resolution, and Contrast to Noise Ratio.
 
Images, Movies, Sliders:
 Fetus (Brain) and Dermoid in Mother  Open this link in a new window
      

Courtesy of  Robert R. Edelman

 Circle of Willis, Time of Flight, MIP  Open this link in a new window
    
SlidersSliders Overview

 Anatomic MRI of the Knee 1  Open this link in a new window
    
SlidersSliders Overview

 Anatomic Imaging of the Liver  Open this link in a new window
      

 Brain MRI Inversion Recovery  Open this link in a new window
    
 
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• View the DATABASE results for 'Contrast' (373).Open this link in a new window


• View the NEWS results for 'Contrast' (77).Open this link in a new window.
 
Further Reading:
  Basics:
Magnetic resonance imaging
   by www.scholarpedia.org    
MRI's inside story
Thursday, 4 December 2003   by www.economist.com    
Image Characteristics and Quality
   by www.sprawls.org    
  News & More:
A natural boost for MRI scans
Monday, 21 October 2013   by www.eurekalert.org    
A groundbreaking new graphene-based MRI contrast agent
Friday, 8 June 2012   by www.nanowerk.com    
New MRI Chemical Offers Amazing Contrast
Friday, 22 January 2010   by news.softpedia.com    
Searchterm 'Image' was also found in the following services: 
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News  (255)  Resources  (73)  Forum  (128)  
 
Fast Spin EchoForum -
related threadsInfoSheet: - Sequences - 
Intro, 
Overview, 
Types of, 
etc.
 
Fast Spin Echo Diagram (FSE) In the pulse sequence timing diagram, a fast spin echo sequence with an echo train length of 3 is illustrated. This sequence is characterized by a series of rapidly applied 180° rephasing pulses and multiple echoes, changing the phase encoding gradient for each echo.
The echo time TE may vary from echo to echo in the echo train. The echoes in the center of the K-space (in the case of linear k-space acquisition) mainly produce the type of image contrast, whereas the periphery of K-space determines the spatial resolution. For example, in the middle of K-space the late echoes of T2 weighted images are encoded. T1 or PD contrast is produced from the early echoes.
The benefit of this technique is that the scan duration with, e.g. a turbo spin echo turbo factor / echo train length of 9, is one ninth of the time. In T1 weighted and proton density weighted sequences, there is a limit to how large the ETL can be (e.g. a usual ETL for T1 weighted images is between 3 and 7). The use of large echo train lengths with short TE results in blurring and loss of contrast. For this reason, T2 weighted imaging profits most from this technique.
In T2 weighted FSE images, both water and fat are hyperintense. This is because the succession of 180° RF pulses reduces the spin spin interactions in fat and increases its T2 decay time. Fast spin echo (FSE) sequences have replaced conventional T2 weighted spin echo sequences for most clinical applications. Fast spin echo allows reduced acquisition times and enables T2 weighted breath hold imaging, e.g. for applications in the upper abdomen.
In case of the acquisition of 2 echoes this type of a sequence is named double fast spin echo / dual echo sequence, the first echo is usually density and the second echo is T2 weighted image. Fast spin echo images are more T2 weighted, which makes it difficult to obtain true proton density weighted images. For dual echo imaging with density weighting, the TR should be kept between 2000 - 2400 msec with a short ETL (e.g., 4).
Other terms for this technique are:
Turbo Spin Echo
Rapid Imaging Spin Echo,
Rapid Spin Echo,
Rapid Acquisition Spin Echo,
Rapid Acquisition with Refocused Echoes
 
Images, Movies, Sliders:
 Lumbar Spine T2 FSE Sagittal  Open this link in a new window
    

Courtesy of  Robert R. Edelman
 MRI - Anatomic Imaging of the Foot  Open this link in a new window
    
SlidersSliders Overview

 Lumbar Spine T2 FSE Axial  Open this link in a new window
    

Courtesy of  Robert R. Edelman
 
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• View the DATABASE results for 'Fast Spin Echo' (31).Open this link in a new window

 
Further Reading:
  Basics:
MYELIN-SELECTIVE MRI: PULSE SEQUENCE DESIGN AND OPTIMIZATION
   by www.imaging.robarts.ca    
Advances in Magnetic Resonance Neuroimaging
Friday, 27 February 2009   by www.ncbi.nlm.nih.gov    
  News & More:
New MR sequence helps radiologists more accurately evaluate abnormalities of the uterus and ovaries
Thursday, 23 April 2009   by www.eurekalert.org    
Spin echoes, CPMG and T2 relaxation - Introductory NMR & MRI from Magritek
2013   by www.azom.com    
MRI Resources 
Pregnancy - Non-English - MRI Reimbursement - Diffusion Weighted Imaging - Claustrophobia - Spine MRI
 
Aliasing ArtifactInfoSheet: - Artifacts - 
Case Studies, 
Reduction Index, 
etc.MRI Resource Directory:
 - Artifacts -
 
Quick Overview
Please note that there are different common names for this MRI artifact.
Artifact Information
NAME
Aliasing, backfolding, foldover, phase wrapping, wrap around
DESCRIPTION
Image wrap around
Aliasing is an artifact that occurs in MR images when the scanned body part is larger than field of view (FOV). As a consequence of the acquired k-space frequencies not being sampled densely enough, whereby portions of the object outside of the desired FOV get mapped to an incorrect location inside the FOV. The cyclical property of the Fourier transform fills the missing data of the right side with data from behind the FOV of the left side and vice versa. This is caused by a too small number of samples acquired in, e.g. the frequency encoding direction, therefore the spectrums will overlap, resulting in a replication of the object in the x direction.
Aliasing in the frequency direction can be eliminated by twice as fast sampling of the signal or by applying frequency specific filters to the received signal.
A similar problem occurs in the phase encoding direction, where the phases of signal-bearing tissues outside of the FOV in the y-direction are a replication of the phases that are encoded within the FOV. Phase encoding gradients are scaled for the field of view only, therefore tissues outside the FOV do not get properly phase encoded relative to their actual position and 'wraps' into the opposite side of the image.
mri safety guidance
Image Guidance
Use a larger FOV, RFOV or 3D Volume, apply presaturation pulses to the undesired tissue, adjust the position of the FOV, or select a small coil which will only receive signal from objects inside or near the coil. The number of phase encoding steps must be increased in phase direction, unfortunately resulting in longer scan times.
When this is not possible it can be corrected by oversampling the data. Aliasing is eliminated by Oversampling in frequency direction. No Phase Wrap (Foldover Suppression) options typically correct the phase encoding by doubling the field of view, doubling the number of phase encodes (to keep resolution constant) and halving the number of averages (to keep scan time constant) then discarding the additional data and processing the image within the desired field of view (but this is more time consuming).
Tissue outside this doubled area can be folded nevertheless into the image as phase wrap. In this case combine more than 2 number of excitations / number of signal averages with foldover suppression.
See also Aliasing, Foldover Suppression, Oversampling, and Artifact Reduction - Aliasing.
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• View the DATABASE results for 'Aliasing Artifact' (11).Open this link in a new window

MRI Resources 
Claustrophobia - Open Directory Project - Knee MRI - Contrast Agents - Pathology - Equipment
 
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