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Result : Searchterm 'Image Acquisition Time' found in 1 term [ ] and 7 definitions [ ], (+ 18 Boolean[ ] results
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(SCT) The total scan time is the time required to collect all data needed to generate the programmed images.
The scan time is related to the used pulse sequence and dependent on the assemble of parameters like e.g., repetition time (TR), Matrix, number of signal averages ( NSA), TSE- or EPI factor and flip angle.
For example, the total scan time for a standard spin echo or gradient echo sequence
is number of repetitions x the scan time per repetition (means the product of repetition time (TR), number of phase encoding steps, and NSA).
See also Number of Excitations, Turbo Spin Echo Turbo Factor, Echo Planar Imaging Factor, Flip Angle and Image Acquisition Time.
See also acronyms for 'scan time parameters' from different manufacturers. | |  | | | | | | | Further Reading: | | Basics:
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The respiratory phase can be used to control imaging either by only acquiring the image data during a particular portion of the respiratory cycle (which increases image acquisition time) or by adjusting the sequence of image data collection according to the phase of the respiratory cycle in such a way as to minimize motion-induced artifacts in the reconstructed image. See also Respiratory Ordered Phase Encoding. | |  | | | |
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Imaging techniques in which NMR signals are gathered from the whole object volume to be imaged at once, with appropriate encoding pulse RF and gradient sequences to encode positions of the spins. Many sequential plane imaging techniques can be generalized to volume imaging, at least in principle. Advantages include potential improvement in signal to noise ratio by including signal from the whole volume at once; disadvantages include a bigger computational task for image reconstruction and longer image acquisition times (although the entire volume can be imaged from the one set of data). Also called simultaneous volume imaging. | | | |  | | • View the DATABASE results for 'Volume Imaging' (7).
| | | • View the NEWS results for 'Volume Imaging' (4).
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(SE) The most common pulse sequence used in MR imaging is based of the detection of a spin or Hahn echo. It uses 90° radio frequency pulses to excite the magnetization and one or more 180° pulses to refocus the spins to generate signal echoes named spin echoes (SE).
In the pulse sequence timing diagram, the simplest form of a spin echo sequence is illustrated.
The 90° excitation pulse rotates the longitudinal magnetization ( Mz) into the xy-plane and the dephasing of the transverse magnetization (Mxy) starts.
The following application of a 180° refocusing pulse (rotates the magnetization in the x-plane) generates signal echoes. The purpose of the 180° pulse is to rephase the spins, causing them to regain coherence and thereby to recover transverse magnetization, producing a spin echo.
The recovery of the z-magnetization occurs with the T1 relaxation time and typically at a much slower rate than the T2-decay, because in general T1 is greater than T2 for living tissues and is in the range of 100-2000 ms.
The SE pulse sequence was devised in the early days of NMR days by Carr and Purcell and exists now in many forms: the multi echo pulse sequence using single or multislice acquisition, the fast spin echo (FSE/TSE) pulse sequence, echo planar imaging (EPI) pulse sequence and the gradient and spin echo (GRASE) pulse sequence;; all are basically spin echo sequences.
In the simplest form of SE imaging, the pulse sequence has to be repeated as many times as the image has lines. Contrast values:
PD weighted: Short TE (20 ms) and long TR.
T1 weighted: Short TE (10-20 ms) and short TR (300-600 ms)
T2 weighted: Long TE (greater than 60 ms) and long TR (greater than 1600 ms)
With spin echo imaging no T2* occurs, caused by the 180° refocusing pulse. For this reason, spin echo sequences are more robust against e.g., susceptibility artifacts than gradient echo sequences.
See also Pulse Sequence Timing Diagram to find a description of the components.
| | | |  | | • View the DATABASE results for 'Spin Echo Sequence' (24).
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In the 1930's, Isidor Isaac Rabi (Columbia University) succeeded in detecting and measuring single states of rotation of atoms and molecules, and in determining the mechanical and magnetic moments of the nuclei.
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Felix Bloch (Stanford University) and Edward Purcell (Harvard University) developed instruments, which could measure the magnetic resonance in bulk material such as liquids and solids. (Both honored with the Nobel Prize for Physics in 1952.) [The birth of the NMR spectroscopy]
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In the early 70's, Raymond Damadian (State University of New York) demonstrated with his NMR device, that there are different T1 relaxation times between normal and abnormal tissues of the same type, as well as between different types of normal tissues.
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In 1973, Paul Lauterbur (State University of New York) described a new imaging technique that he termed Zeugmatography. By utilizing gradients in the magnetic field, this technique was able to produce a two-dimensional image (back-projection). (Through analysis of the characteristics of the emitted radio waves, their origin could be determined.) Peter Mansfield further developed the utilization of gradients in the magnetic field and the mathematically analysis of these signals for a more useful imaging technique. (Paul C Lauterbur and Peter Mansfield were awarded with the 2003 Nobel Prize in Medicine.)
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1977/78: First images could be presented.
A cross section through a finger by Peter Mansfield and Andrew A. Maudsley.
Peter Mansfield also could present the first image through the abdomen.
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In 1977, Raymond Damadian completed (after 7 years) the first MR scanner (Indomitable). In 1978, he founded the FONAR Corporation, which manufactured the first commercial MRI scanner in 1980. Fonar went public in 1981.
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1981: Schering submitted a patent application for Gd-DTPA dimeglumine.
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1982: The first 'magnetization-transfer' imaging by Robert N. Muller.
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In 1983, Toshiba obtained approval from the Ministry of Health and Welfare in Japan for the first commercial MRI system.
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1986: Jürgen Hennig, A. Nauerth, and Hartmut Friedburg (University of Freiburg) introduced RARE (rapid acquisition with relaxation enhancement) imaging. Axel Haase, Jens Frahm, Dieter Matthaei, Wolfgang Haenicke, and Dietmar K. Merboldt (Max-Planck-Institute, Göttingen) developed the FLASH ( fast low angle shot) sequence.
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1988: Schering's MAGNEVIST gets its first approval by the FDA.
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In 1991, fMRI was developed independently by the University of Minnesota's Center for Magnetic Resonance Research (CMRR) and Massachusetts General Hospital's (MGH) MR Center.
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From 1992 to 1997 Fonar was paid for the infringement of it's patents from 'nearly every one of its competitors in the MRI industry including giant multi-nationals as Toshiba, Siemens, Shimadzu, Philips and GE'.
| | | |  | | • View the DATABASE results for 'MRI History' (6).
| | | • View the NEWS results for 'MRI History' (1).
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