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Result : Searchterm 'Equilibrium' found in 7 terms [] and 29 definitions []
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Searchterm 'Equilibrium' was also found in the following services: 
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Resources  (1)  
 
Spin Spin Relaxation
 
(T2) The return of the transverse magnetization to its equilibrium value, zero.
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• Related Searches:
    • Spin Lattice Relaxation
    • T1 Time
    • T2* Time
    • Spin Spin Relaxation Time
    • T2 Weighted
 
Further Reading:
  Basics:
Spin echoes, CPMG and T2 relaxation - Introductory NMR & MRI from Magritek
2013   by www.azom.com    
Searchterm 'Equilibrium' was also found in the following service: 
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Radiology  (3) Open this link in a new window
Steady State Coherent
 
A state of spins, which leads to an equilibrium magnetization for the longitudinal and transverse magnetization, or, when the magnetization at, or after, each RF pulse is the same as in the previous pulse.
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Steady State Free PrecessionInfoSheet: - Sequences - 
Intro, 
Overview, 
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etc.MRI Resource Directory:
 - Sequences -
 
(SFP or SSFP) Steady state free precession is any field or gradient echo sequence in which a non-zero steady state develops for both components of magnetization (transverse and longitudinal) and also a condition where the TR is shorter than the T1 and T2 times of the tissue. If the RF pulses are close enough together, the MR signal will never completely decay, implying that the spins in the transverse plane never completely dephase. The flip angle and the TR maintain the steady state. The flip angle should be 60-90° if the TR is 100 ms, if the TR is less than 100 ms, then the flip angle for steady state should be 45-60°.
Steady state free precession is also a method of MR excitation in which strings of RF pulses are applied rapidly and repeatedly with interpulse intervals short compared to both T1 and T2. Alternating the phases of the RF pulses by 180° can be useful. The signal reforms as an echo immediately before each RF pulse; immediately after the RF pulse there is additional signal from the FID produced by the pulse.
The strength of the FID will depend on the time between pulses (TR), the tissue and the flip angle of the pulse; the strength of the echo will additionally depend on the T2 of the tissue. With the use of appropriate dephasing gradients, the signal can be observed as a frequency-encoded gradient echo either shortly before the RF pulse or after it; the signal immediately before the RF pulse will be more highly T2 weighted. The signal immediately after the RF pulse (in a rapid series of RF pulses) will depend on T2 as well as T1, unless measures are taken to destroy signal refocusing and prevent the development of steady state free precession.
To avoid setting up a state of SSFP when using rapidly repeated excitation RF pulses, it may be necessary to spoil the phase coherence between excitations, e.g. with varying phase shifts or timing of the exciting RF pulses or varying spoiler gradient pulses between the excitations.
Steady state free precession imaging methods are quite sensitive to the resonant frequency of the material. Fluctuating equilibrium MR (see also FIESTA and DRIVE)and linear combination SSFP actually use this sensitivity for fat suppression. Fat saturated SSFP (FS-SSFP) use a more complex fat suppression scheme than FEMR or LCSSFP, but has a 40% lower scan time.
A new family of steady state free precession sequences use a balanced gradient, a gradient waveform, which will act on any stationary spin on resonance between 2 consecutive RF pulses and return it to the same phase it had before the gradients were applied.
This sequences include, e.g. Balanced Fast Field Echo - bFFE, Balanced Turbo Field Echo - bTFE, Fast Imaging with Steady Precession - TrueFISP and Balanced SARGE - BASG.

See also FIESTA.
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• View the DATABASE results for 'Steady State Free Precession' (20).Open this link in a new window

 
Further Reading:
  News & More:
Comparison of New Methods for Magnetic Resonance Imaging of Articular Cartilage(.pdf)
2002
Searchterm 'Equilibrium' was also found in the following services: 
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Resources  (1)  
 
T1 Relaxation
 
The return to equilibrium (high energy protons returns to the low energy state) within the lattice is named the T1, spin lattice or longitudinal relaxation. During the time T1, the spinning protons realign with the external magnetic field with an exchange of their energy, resulting in heat. The value of the T1 time depends of the tissues ability for energy exchange.

See also Longitudinal Relaxation Time.
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• View the DATABASE results for 'T1 Relaxation' (18).Open this link in a new window

 
Further Reading:
  Basics:
Musculoskeletal MRI at 3.0 T: Relaxation Times and Image Contrast
Sunday, 1 August 2004   by www.ajronline.org    
  News & More:
MRI's inside story
Thursday, 4 December 2003   by www.economist.com    
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Radiology  (3) Open this link in a new window
Time of Flight AngiographyInfoSheet: - Sequences - 
Intro, 
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Types of, 
etc.MRI Resource Directory:
 - MRA -
 
(TOF) The time of flight angiography is used for the imaging of vessels. Usually the sequence type is a gradient echo sequences with short TR, acquired with slices perpendicular to the direction of blood flow.
The source of diverse flow effects is the difference between the unsaturated and presaturated spins and creates a bright vascular image without the invasive use of contrast media. Flowing blood moves unsaturated spins from outside the slice into the imaging plane. These completely relaxed spins have full equilibrium magnetization and produce (when entering the imaging plane) a much higher signal than stationary spins if a gradient echo sequence is generated. This flow related enhancement is also referred to as entry slice phenomenon, or inflow enhancement.
Performing a presaturation slab on one side parallel to the slice can selectively destroy the MR signal from the in-flowing blood from this side of the slice. This allows the technique to be flow direction sensitive and to separate arteriograms or venograms. When the local magnetization of moving blood is selectively altered in a region, e.g. by selective excitation, it carries the altered magnetization with it when it moves, thus tagging the selected region for times on the order of the relaxation times.
For maximum flow signal, a complete new part of blood has to enter the slice every repetition (TR) period, which makes time of flight angiography sensitive to flow-velocity. The choice of TR and slice thickness should be appropriate to the expected flow-velocities because even small changes in slice thickness influences the performance of the TOF sequence. The use of sequential 2 dimensional Fourier transformation (2DFT) slices, 3DFT slabs, or multiple 3D slabs (chunks) are depending on the coverage required and the range of flow-velocities.
3D TOF MRA is routinely used for evaluating the Circle of Willis.

See also Magnetic Resonance Angiography and Contrast Enhanced Magnetic Resonance Angiography.
 
Images, Movies, Sliders:
 TOF-MRA Circle of Willis Inverted MIP  Open this link in a new window
    

 Circle of Willis, Time of Flight, MIP  Open this link in a new window
    
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Radiology-tip.comradCT Angiography,  Coronary Angiogram
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Medical-Ultrasound-Imaging.comColor Power Angio,  Doppler Ultrasound
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• View the DATABASE results for 'Time of Flight Angiography' (11).Open this link in a new window

 
Further Reading:
  Basics:
MR–ANGIOGRAPHY(.pdf)
  News & More:
Magnetic resonance angiography: current status and future directions
Wednesday, 9 March 2011   by www.jcmr-online.com    
MRI Resources 
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