GB2217847A - Nmr imaging spectroscopy system - Google Patents

Nmr imaging spectroscopy system Download PDF

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GB2217847A
GB2217847A GB8809956A GB8809956A GB2217847A GB 2217847 A GB2217847 A GB 2217847A GB 8809956 A GB8809956 A GB 8809956A GB 8809956 A GB8809956 A GB 8809956A GB 2217847 A GB2217847 A GB 2217847A
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nmr
responses
generating
nmr spectrum
desired portion
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GB8809956D0 (en
GB2217847B (en
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Roger J Ordidge
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National Research Development Corp UK
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National Research Development Corp UK
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Priority to EP89304170A priority patent/EP0339979B1/en
Priority to DE68927418T priority patent/DE68927418T2/en
Priority to US07/343,205 priority patent/US5051698A/en
Priority to JP1109020A priority patent/JP2960937B2/en
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    • GPHYSICS
    • G01MEASURING; TESTING
    • G01RMEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
    • G01R33/00Arrangements or instruments for measuring magnetic variables
    • G01R33/20Arrangements or instruments for measuring magnetic variables involving magnetic resonance
    • G01R33/44Arrangements or instruments for measuring magnetic variables involving magnetic resonance using nuclear magnetic resonance [NMR]
    • G01R33/48NMR imaging systems
    • G01R33/54Signal processing systems, e.g. using pulse sequences ; Generation or control of pulse sequences; Operator console
    • G01R33/56Image enhancement or correction, e.g. subtraction or averaging techniques, e.g. improvement of signal-to-noise ratio and resolution

Description

... r Z4 IMPROVEMENTS IN OR RELATING TO NMR IMAGING SYSTEMS The present
invention relates to NMR imaging spectroscopy systems and more particularly to the selection of specific small volumes within a bodv and to the production of NMR spectra in respect of such small volumes.
Several techniques have been used to produce high resolution in-vivo NMR spectra from selected cubes whose position can be related to an MR image of the subject (R.J. Ordidge, A. Connelly and J.A.B. Lohman; J. Magn. Reson. 66, '283 (1986 ISIS Technique) and D.M. Doddrell, W.M. Brooks, J.M. Bulsing, J. Field, M.G. Irving and H.Baddeley; J. Magn. Reson. 68, 376 (1986)). Whilst aLl these methods have certain disadvantages. the ISIS technique has proved to be the most easy to use, especially when investigating energy metabolism by phosphorous NMR spectroscopy. The main disadvantage of the ISIS method is that cube selection can only be achieved by the cancellation of large amounts of signal originating from volumes of tissue outside the region of interest. The signal to be investigated is sometimes small in comparison, and errors in the cancellation proces-s, which can be caused by spectrometer instability, are sometimes visible in the resulting spectrum. This problem has now been solved by the use of a selective noise pre-pulse (R.J. Ordidge; Magn. Reson. Med. 5, 93 (1987)) which ra ndomises unwanted spin magnetisatioq a prior to the ISIS experiment. The noise pulse is particularly effective since it randomises the longitudinal spin magnetisation and therefore retains one of the principle advantages of the ISIS technique, namely ,the insensitivity to the applied radio frequency power level.
A different approach to spatial selection uses the technique of chemical. shift imaging (A.A. Maudsley, S.K. Hilal, W.H. Perman and H.E. Simon: J. Magn. Reson. 51, 1 1 i / -j., U 2 147 (1983)). Recent advances in technology have enabled this method to be applied in-vivo to the determination of the spatial distribution of phosphorus metabolites. The removal of eddy currents following gradient pulses by the use of actively shielded gradient coils (P. Mansfield and B. Chapman, J. Phys. E: Sci. Instrum. 19, 540 (1986)), has resulted in the acquisition of NMR spectra with minimal delay following the radiofrequency (RF) pulse (I.J. Cox. D.J. Bryant, B.D. Ross, I.R. Young, D.G. Gadiam, G.M. Bydder, S.R. Williams, A.L. Busza and T.E. Bates, Magn. Reson. Med. 5, 186 (1987)). The previous disadvantage of this method was the deve ndence of acquired spectra upon the spin-spin relaxation time. Although this has now been markedl-,- reduced, this dependence can never be completelv eliminated, and the short delay prior to data acquisition (approximately two milliseconds) results in the absence of broad resonance lines in the acquired spectrum (linewidths greater than about 500 Hz), and a slight reduction in signal to noise ratio. Since most of the interesting resonances produce narrow linewidths, the former disadvantage usually only causes phase and baseline artefacts in the resulting spectrum. A further disadvantage of this technique is the relatively long experimental time required to complete a chemical shift imaging experiment. This is typically fifteen minutes for a two dimensional spatial resolution of32x32, and therefore prevents the method being used time-course studies on a shorter time scale.
The advantage of chemical shift imaging is that once the experiment has been completed, the data contains an NMR spectrum from each of the elements in the two or three dimensional spatial array. Most of this data is not required; however it must be acquired as part of the imaging process.
3 The object of the present invention is to provide an extension of the ISIS technique which allows the selection of multiple volumes of material, and in which a compromise can be made between experimental duration and the number size arid location of the selected cubes.
According to the present invention there is provided a method of generating an NNMR spectrum of a desired portion of an object including obtaining M- NMR responses of the object, each response comprising information from a plurality of smaller volumes within said obJect and combining together M subtraction to voitimes. The bodv.
NMR number system.
intensity of NMR responses by addition or obtain responses from selected smaller said obJect can be a portion of a 1.arger In a preferred embodiment in the total sequence of M responses each small volume experiences an even of inversions or double inversions of the spin Embodiments of the present invention. will now be described, by way of example with reference to the accompanying drawings in which:- Figure 1 illustrates the effect of the sequence of four ISIS experiments required to determine the volume elements of a 2x2 image matrix. Iii represents the the relevant volume element. Hatched elements experience a single inversion of the NMR spins, whilst cross-hatched elements experience two inversions.4,;E For example, in experiment B2, one inversion pulse i4 applied along each axis of the sample, resulting in the lower right hand element experiencing a double inversion of the spin system; Figure 2 shows the spatial distribution of spin inversions required to determine the individual elements of a single 4x4 image matrix. Hatched elements experience a inversion, and cross-hatched elements a double inversion. In experiment D4 for example. the two central columns and the two central rows are inverted. giving a double inversion of the four central cubes; Figure 3 shows the spatial distribution of spin inversions for a modified seauence that eliminates the signal from all volume elements around the edge of the sample, and enables the signal from each of the four central elements to be individually determined; Figure 4(A) shows an irregular volume (solid line) subdivided into a 7x5 matrix of cubes. In order to prevent the detection of signal from volumes outside the region of interest, only the signal from the shaded cubes are useful in a spatially localized NMR experiment; and Figure 4(B) shows exactly the same spatial distribution of useful signal may be measured in an ISIS experiment consisting of 4x4 rectangular volume elements of varying size. A saving in experimental time may thus be achieved.
With reference now to the drawings, in order to simplify the problem, it is beneficial to consider a 2x2 matrix re-presenting, a simple imaae, as shown in Figure 1. The aim is to obtain signals from any of the four squares, by linear combination of the results from a sequence of experiments. The method may then be extended to larger arrays by aprocess of subdivision of array elements and repetition of the principle of the technique. Let us suppose that we have an image which ca.y be represented by the 2x2 matrix given below 115) 1 f = 1 1 9J (1) Each element of the matrix li,j corresponds to the intensity of signal generated in a region of real space. It is useful to adopt a binary notation so that i = 0,1 and j = 0,1.
J 1 1 The matrices 0' 0 = 1 11 1 1 1 1 1 j 1 0 = i f i 1 - 1 - 11 R0,1 1 1 11 - 11 i 1 -lj R], 1 1 - 11 L1 (2) correspond to the operation of inversion of t he NMR spins in that region of real space only when the element is -1. A selective 1800 pulse is used to achieve this goal, and note that M', 1 requires the application of two selective pulses. If the element is +1, then the spins are not inverted, or have been inverted twice. The effect of this inversion is represented diagrammatically in Figure 1, where hatched elements have experienced a single inversion pulse, and cross-hatched elements have received two pulses. Each matrix therefore corresponds to an individual NMR experiment. We denote these matrices by M', 13, where o(,B is a label for the matrix and not an index. We also denote P4f,,j to be the i,jth matrix element v of matrix M,13, where i,j = 0,1.
The matrix ik. ú3 has column j=1 with their spins inverted if 3=1, and the spins not inverted if AFO. Similarly the if -=0. Thus j=1 inverted twice to end Signals by row i=l is inverted if o=1 and not inverted the matrix M', 1 has both row i=l and column, and M, 1 =1 as the spins have been inverted j 1 up aligned with the field.
S', 13 are acquired in each experiment given 1, = - -cc, 3 - S M i ' j j (3) 6 These are the result of flipping the spins in rows and columns as defined by the matrices IM",0 and then measuring the NMR signal. For the image matrix of equation (1, we readily find signals SO,0 =28, SO.' =8, S'. 0 = -20 and SI. 1 = -4.
From these projected signals we -can recover the original matrix by the following procedure. Another set of matrices are created -i R 1 51 7 ao,o 1 01, RO, 1 0 1 0 0 o0 1 0 0 01 0 01 1 011 1 which are related to the w.atrices"P' (as can be seen by working out each example) by the formula (4) + j 'j = 1/4 71= 3 Q (- 1) ri = 0 These matrices simply select the signal from the desired quadrant. The purpose of this procedure is to determine which is the signal from each quadrant. By evaluating each example the reader can establish that Y Y ji =. Y-,-,-JY6 and hence application of 'j selects the signal from the j,ith cube.
Substitution of equation (5) into (6) gives 1/4 l 71 (- 1 ec=o =0 1 -, 1 1/4 ' 0 -, c 0 For our elementary example (ai + 0j) "-ot,6 - Mk,t 1 -2-, k k 9, (_0 (ai + 6j) S a,B (6) e 8 11 0 1/4 (SO, 0 + SO, 1 + S' 0 + S' 1 3 1/4 (SO, 0 + SO. 1 - S' 0 - S1 1 15 1/4 (SO, 0 - SO, 1 + S' 0 - S' 1 1 = 1/4(S0.0 -Soil -Slio +sl,l) =9 Therefore, four signal measurements can be combined in linear combinations to determine each of the four signal components in a 2x2 matrix. The extension to three dimensional images is straightforward.
It is more difficult to see how to extend this technique to 4x4 matrices, and then to 8x8 etc. We do this by taking 4x4 matrices as direct products (A.W. Joshi; "Matrices and Tensors in Physics", p. 138, Wiley Eastern Ltd. , New Delhi (1975)) of the matrices'Mcc," r,.to B ply : 0,0 -;m ' 1 M 1 1,0 S F1YO m 0,1 -a 6 -Y6 m ' m 1 9 1 1 j For example one of the 16 such 4x4 matrices is C -I, 1 1 ' m F4 E1,0 0 E], 1 = 1 - 1,1 _M -H], r+l 1 + 1 1-1 + 1 - 1 + 1 - 1 +1 -1 +1 +1 -1 +1 z J 1 1 1 4 X 1 9 In order to obtain this sign dependence of the image signal the 2nd and 3rd rows of NMR spins should be inverted, and the 2nd and 4th columns.
Let us label the element of the above matrix by row k, column t, so that this element is N1,0;1,1. From these r', C 16 4x4 matrices we obtain signals S k,;i, N kP, Z,k where 9,,k = 0, 1,2,3 Once again we want to reconstruct the image from these signals. We do this using the same procedure, constructing new matrices = ijo i'j 1 1/4 L,C4=0 5=0)a f =0 This matrix is non zero only for element AE k 1, 11 where At- = 2i +i and k = 2j +j. In the same way we obtain r- - 1 71 71 I = 1/42 11. (- 1) (cxi+Bj+(yl i 1 +P, t j 1) k,' LCI=0 -=o -0t, =0 i,,=0 S ctB; al c 1 The extension to 8x8 is now clear; one constructs a 4"'r - matrix from M90160;. 4t.,ep, and projects out the signals from them.
This technique provides a means of reconstructing discrete images of an object without using a Fourier transformation. A sequence of selective inversion pulses 11 10are used to invert strips of the object along orthogonal directions. Data acquisition consists of measurement of the intensity of the resultant signal. If the NIMR measurement experiment consists of a 900 pulse in the absence of field gradients, the chemical spectrum of each volume element can be determined in a similar manner to the ISIS method (R.J. Ordidge, A. Connelly and J.A.B. Lohman: J. Magn. Reson. 66, 283 (1986)).
The preferred method requires the application of N2 experiments to determine the chemical spectrum from NxN matrix of cubic volume elements where n = 2P bLnd p is an inteaer. Each experiment requires the application of up eventually imposes a limit to the array size. Figure 2 shows the sDatial distribution of inversions for selection of a 4x4 matrix. Slice selection usin!R' the ISIS -Drincinle necessitates an extra inversion pulse and a doubling of the number of experiments to 2N2.
A disadvantage of this method is that if the image matrix spans the overall dimensions of the object, the extremities of the object should ideally experience a perfect 180() spin nutation at the relevant times in the experimental sequence. Clearly in the practical situation with inhomogeneous RF transmitter coils and extended specimens, this is not possible. A better approach is therefore to remove the signal from the majority of the subject using the standard ISIS technique, and apply the principle described earlier to subdivide the selected large cube into an NxN matrix of smaller cubes. In two dimensions. a sequence of 4 experiments is required to select the central volume, and this must be multiplied by the number of experiments required to further subdivide the central cube into a 2x2 or 4x4 matrix etc. The outer loop of 4 experiments ensures cancellation of large regions of unwanted signal surrounding the central to N selective inversion pulses. which 4 c X A 11 volumes of interest where experimental errors might have compromised the accuracy of all measurements in the data set, if the normal procedure had been applied to the whole sample.
Figure 3 shows a modified sequence of selective inversions based on this principle. In this example the total experimental sequence now consists of 16 experiments, and the purpose is to determine the individual spectra from a 2x2 matrix in the centre of the object whilst eliminating all peripheral volume elements. If sl.,Lee selection is applied using the ISIS principle along the third axis, the full experimental sequence would require 32 experiments. An advantage of this sequence is that in the determination of the spectra from each of the central four volume elements, the signal from all other cubes cancels perfectly. Elaborating on this point, the same volume of material experiences an even number of inversions and double inversions during the sequence. Since experimental errors might occur, we can assume that double inversion is not equivalent to leaving the NMR spins unperturbed. The linear combination for perfect cancellation of these signals must therefore result in cancellation of like signals. Another property of this combination procedure, is that the signal from each cube should always add without cancellation, whilst all other signals should be completely destroyed. The resultant signal to noise ratio is therefore equivalent to that obtainable by isolating the volume element'in some other way (e.g. surgically), and performing an equal number of straightforward 900 pulse-acquire NMR experiments.
Extension of this principle to determine the individual spectra from NxN cubes and including slice selection, requires a sequence of 8N2 experiments with up to '41.N+1 selective inversion pulses per experiment. For example, with 8x8 cubes, we require 512 experiments and j 12 up to 17 selective inversion pulses. If the RF pulse proposed by (M.S. Silver, R.I. Joseph and D.I. Hoult; J. Magn. Reson.
09 349 (1984)) is used for selective inversion, a practical pulse length is typically 120 milliseconds. Seventeen selective pulses would therefore probably result in an unacceptable weighting of the acquired spectra through the effects of spin lattice relaxation.
T there are, however, two main advantages of this general aPproach. Firstl-y-, each volume element need not be cubic, and the technique allows for different size elements within a si-n--Ie sequence. if the signal from ad.jacent cubes i 's added toze the r, this enables an irregular seiectlve vo-Lume to be more easily covered by a mosaic of different size rectangular volumes, provided they fit within a non-uniform grid. This is illustrated ure 4(A) shows an irregular-shaped volume in Figure 4. Fiwhich can be adequately represented by a 7x5 matrix of cubes. Figure 4(B) shows the same shaped volume covered with exactly the same efficiency using a 4x4 matrix of rectangular volume elements of varying size. A corresponding reduction in the number of ISIS volume elements would result in a reduction of the minimum number of ISIS experiments required to investigate this sample volume. Secondly the elements need not be adjacent in space, and mav be separated to investigate different body organs within a single experiment.
-;F It may be more efficient to produce certain shapea volumes by subtraction of different size rectangular volumes rather than by extension of the matrix size.
The general Principle of reconstructing spectra using pLddition and subtraction of signals with different inversions and double inversions can be extended uD to an image matrix of dimensions 2P x 21q where p and q are integers.
1 J 1 r 1 13 The present invention provides a theoretical basis for the extension of the ISIS technique to multiply defined volumes. These are useful for the investigation of irrei4ular tissue volumes because the signal from a series of volume elements can be subsequently coadded. Alternatively, several volume elements positioned in different regions of the subJect can be simultaneously increase in efficiency and utility of' the NMR spectrometer. The practical -Limitation is the number of selective inversion pulses which may be applied in quick succession. The total duration should be Less than one tenth of the spin lattice relaxat-ion time to minimize distortion of the measured in-vivo spectrum through spin-Lattice relaxation during the pre-Pulse period. Therefore a iDractical approach might be to use an Rrray of 4x4 volume elements 28 requiring 14 experiments with up to 9 selective inversion pulses. This will probably cover regions of the specimen with the equivalent spatial definition of a much larger array obtainable by chemical shift imaging. Furthermore if a selective 900 pulse is used in ISIS for signal acquisition combined with slice definition, in a similar manner to the chemical shift imaging experiment, the number of experiments is immediately reduced by a factor of two. Finally, we would like to point out that system instability and dynamic range limitations can cause as many problems in chemical shift imagi,E experiments as in ISIS. However, the option to selectively randomise unwanted signal using a noise pulse (R.J. Ordid-de; iMagn. Reson. Med. 5, 93 (1987)) is available in both experiments.
investigated with a corresponding; 1 J.
1 14

Claims (10)

1 A method of generating an NMR spectrum of a desired portion of an object including obtaining M NMR responses of the object, each response comprising information from a plurality of smaller volumes within said object and combining together the M NMR responses by addition or subtraction to obtain responses from selected smaller volumes.
2. A method of generating an NMR spectrum as claimed in Claim 1 in which the said object is a portion of a larger body.
3. A method of generating an NMR spectrum as claimed in Claim 1 or Claim 2 in which in the total sequence of M NMR responses each small volume experiences an even number of inversions of the spin system.
4. A method of generating an NMR spectrum as claimed- in Claim 1 or Claim 2 in which in the total sequence of M NMR responses each small volume experiences an even number of double inversions of the spin system.
5. Apparatus for generating an enhanced NMR spectrum of a desired portion of an object including means for obtaining M NMR responses of the object wherein each response comprises information froma Plurality of smaller volumes within said object and addition or subtraction means for combining together the M NMR. responses by addition "or subtraction to obtain responses from selected smaller volumes.
6. Apparatus for gene rating an enhanced NMR spectrum of a desired portion of an object as claimed in Claim 5 in which the said object is a portion of a larger object.
7. Apparatus for generating an enhanced NMR spectrum of a desired portion of an object as claimed in Claim 5 or Claim 6 including means for subjecting each small volume to an even number of inversions of the spin system for the total sequence of M NMR responses.
4 i
8. Apparatus for generating an enhanced NMR spectrum of a desired portion of an object as claimed in Claim 5 including means for subjecting each small volume to an even number of double inversions of the spin system for the total sequence of M NMR responses.
9. A method of generating an NMR spectrum of a desired portion of an object substantially as described with reference to the accompanying drawings.
10. Apparatus for generating an enhanced NMR spectrum of a desired portion of an object substantially a described with reference to the accompanying drawings.
dhed 1 98j59_)st The p&"ni. Bttte House, 66,71 High Holbom London WC1R 4"M Further copies maybe obt Lined from The -Pnt Otace.
GB8809956A 1988-04-27 1988-04-27 Improvements in or relating to nmr imaging systems Expired - Lifetime GB2217847B (en)

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GB8809956A GB2217847B (en) 1988-04-27 1988-04-27 Improvements in or relating to nmr imaging systems
EP89304170A EP0339979B1 (en) 1988-04-27 1989-04-26 Improvements in or relating to NMR imaging system
DE68927418T DE68927418T2 (en) 1988-04-27 1989-04-26 Magnetic resonance imaging system
US07/343,205 US5051698A (en) 1988-04-27 1989-04-26 NMR imaging systems
JP1109020A JP2960937B2 (en) 1988-04-27 1989-04-27 Method for generating an NMR spectrum of a desired portion of an object

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Families Citing this family (11)

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Publication number Priority date Publication date Assignee Title
GB8819753D0 (en) * 1988-08-19 1988-09-21 Nycomed As Apparatus
DE4313631C1 (en) * 1993-04-26 1994-09-22 Hennig Juergen Magnetic resonance imaging method for the localization of discrete details within a measurement object
DE19609839A1 (en) * 1996-03-13 1997-09-18 Philips Patentverwaltung MR spectroscopy method
US7620440B2 (en) * 2002-05-17 2009-11-17 Case Western Reserve University Direct temporal encoding of spatial information
US7715900B2 (en) * 2002-12-19 2010-05-11 University Of Washington Quadruple inversion recovery for quantitative contrast-enhanced black blood imaging
US7627359B2 (en) * 2002-12-19 2009-12-01 University Of Washington Quantitative contrast enhanced black-blood imaging using quadruple-inversion recovery
US7253627B1 (en) 2006-07-19 2007-08-07 Univ King Fahd Pet & Minerals Method for removing noise from nuclear magnetic resonance signals and images
WO2008144421A1 (en) * 2007-05-17 2008-11-27 University Of Washington Fast two-point mapping of the bound pool fraction and cross-relaxation rate constant for mri
WO2009117211A2 (en) * 2008-03-18 2009-09-24 University Of Washington Improved motion-sensitized driven equilibrium blood-suppression sequence for vessel wall imaging
TWI395966B (en) * 2009-01-17 2013-05-11 Univ Nat Taiwan Method of time-domain magnetic resonance imaging and device thereof
DE102011080793B4 (en) 2011-08-11 2013-05-29 Siemens Aktiengesellschaft MR method with flexible adaptation of acquisition and evaluation parameters for subareas of a target volume

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0212734A1 (en) * 1985-08-08 1987-03-04 Koninklijke Philips Electronics N.V. Method for obtaining nuclear-magnetic resonance spectra
EP0217578A2 (en) * 1985-09-25 1987-04-08 Picker International Limited Nuclear magnetic resonance methods and apparatus

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4297637A (en) * 1978-07-20 1981-10-27 The Regents Of The University Of California Method and apparatus for mapping lines of nuclear density within an object using nuclear magnetic resonance
US4599565A (en) * 1981-12-15 1986-07-08 The Regents Of The University Of Calif. Method and apparatus for rapid NMR imaging using multi-dimensional reconstruction techniques
DE3209264A1 (en) * 1982-03-13 1983-09-22 Bruker Medizintechnik Gmbh, 7512 Rheinstetten METHOD FOR MEASURING THE MAGNETIC CORE RESONANCE FOR NMR TOMOGRAPHY
EP0182873A1 (en) * 1984-06-01 1986-06-04 Advanced Nmr Systems Inc. Nmr fourier imaging from multiple echoes
US4689567A (en) * 1984-06-01 1987-08-25 Advanced Nmr Systems, Inc. NMR Fourier imaging from multiple echoes
US4728893A (en) * 1985-07-31 1988-03-01 The Regents Of The University Of California Increased signal-to-noise ratio in magnetic resonance images using synthesized conjugate symmetric data
IL82029A (en) * 1987-03-27 1990-07-26 Elscint Ltd Method for performing magnetic resonance studies of restricted volumes
US4733185A (en) * 1987-06-01 1988-03-22 General Electric Company Methods for localization in NMR spectroscopy
JPH01170446A (en) * 1987-12-25 1989-07-05 Yokogawa Medical Syst Ltd Method for limiting region of nuclear magnetic resonance image diagnostic apparatus

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0212734A1 (en) * 1985-08-08 1987-03-04 Koninklijke Philips Electronics N.V. Method for obtaining nuclear-magnetic resonance spectra
EP0217578A2 (en) * 1985-09-25 1987-04-08 Picker International Limited Nuclear magnetic resonance methods and apparatus

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EP0339979A3 (en) 1990-12-19
GB8809956D0 (en) 1988-06-02
EP0339979A2 (en) 1989-11-02
JP2960937B2 (en) 1999-10-12
EP0339979B1 (en) 1996-11-06
JPH0217035A (en) 1990-01-22
DE68927418D1 (en) 1996-12-12
US5051698A (en) 1991-09-24
DE68927418T2 (en) 1997-03-06
GB2217847B (en) 1993-02-03

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