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 SHOT          Selection with High-Order gradienT 
Searchterm 'Shot' was found in the Abbreviation Register. 
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Shot
 
Shots are split phase encoding steps (sub-acquisitions).
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Further Reading:
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Utility of the FIESTA Pulse Sequence in Body Oncologic Imaging: Review
June 2009   by www.ajronline.org    
Searchterm 'Shot' was also found in the following services: 
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Fast Low Angle ShotInfoSheet: - Sequences - 
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(FLASH) A fast sequence producing signals called gradient echo with low flip angles. FLASH sequences are modifications, which incorporate or remove the effects of transverse coherence respectively.
FLASH uses a semi-random spoiler gradient after each echo to spoil the steady state (to destroy any remaining transverse magnetization) by causing a spatially dependent phase shift. The transverse steady state is spoiled but the longitudinal steady state depends on the T1 values and the flip angle. Extremely short TR times are possible, as a result the sequence provides a mechanism for gaining extremely high T1 contrast by imaging with TR times as brief as 20 to 30 msec while retaining reasonable signal levels. It is important to keep the TE as short as possible to suppress susceptibility artifacts.
The T1 contrast depends on the TR as well as on flip angle, with short TE.
Small flip angles and short TR results in proton density, and long TR in T2* weighting.
With large flip angles and short TR result T1 weighted images.

TR and flip angle adjustment:

TR 3000 ms, Flip Angle 90°
TR 1500 ms, Flip Angle 45°
TR 700 ms, Flip Angle 25°
TR 125 ms, Flip Angle 10°

The apparent ability to trade TR against flip angle for purposes of contrast and the variation in SNR as the scan time (TR) is reduced.

See also Gradient Echo Sequence.
 
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 Fetus (Brain) and Dermoid in Mother  Open this link in a new window
      

Courtesy of  Robert R. Edelman

 
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Further Reading:
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Motion Compensation in MR Imaging
   by ccn.ucla.edu    
Turbo-FLASH Based Arterial Spin Labeled Perfusion MRI at 7 T
Thursday, 20 June 2013   by www.plosone.org    
Usefulness of MR Imaging for Diseases of the Small Intestine: Comparison with CT
2000   by www.ncbi.nlm.nih.gov    
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Multi Shot Technique
 
When a multi shot technique is applied, each shot will have its own effect on the prepulse, with a scan time increase. Multiple shots allow a shorter IR delay but at the cost of increased scan time.
In multi shot technique (also called mosaic imaging), a group of samples, which are contiguous in k space are acquired in the same sequence repetition. The phase encoding steps or profiles are split into 'shots' (sub-acquisitions). The shot interval is the time between the shots. Usually kept as short as possible. Because the acquisitions are divided into different shots, each shot will have less T1 variation, thereby increasing T1 contrast. Two excitations, each requiring the data for one half of k-space, are the simplest variation of multi shot techniques (e.g. positive versus negative phase encoding). The alternative to this mosaic strategy for multi shot EPI is interleaving. In interleaved sequences, each repetition acquires every nth (n is the number of shots) line in k-space and for the complete raw data set the various repetition data are interlaced.

See also Single Shot Technique.
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Single Shot Technique
 
In single shot techniques (used for EPI, TSE, FSE, RARE, HASTE), the entire raw data set is acquired with a single excitation pulse. The magnetization of a fully relaxed spin system is used. Each of the subsequent echoes is given a different phase encoding. For improved SNR, spatial resolution or FOV, the needed raw data are acquired over a number of sequence repetitions. Each repetition then collects a fraction of the complete raw data set. Only slightly more than a half of the raw data is acquired. The image is obtained through half Fourier reconstruction.
A single shot sequence is useful in cases where movement is to expect e.g. in abdominal Imaging or fetal MRI.

See also Half Fourier Acquisition Single Shot Turbo Spin Echo.
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Further Reading:
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Clinical evaluation of a speed optimized T2 weighted fast spin echo sequence at 3.0 T using variable flip angle refocusing, half-Fourier acquisition and parallel imaging
Wednesday, 25 October 2006
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