Jump to content

MRI pulse sequence

From Wikipedia, the free encyclopedia
(Redirected from Gradient Recalled echo MRI)
Timing diagram for a spin echo type of pulse sequence.

An MRI pulse sequence in magnetic resonance imaging (MRI) is a particular setting of pulse sequences and pulsed field gradients, resulting in a particular image appearance.[1]

A multiparametric MRI is a combination of two or more sequences, and/or including other specialized MRI configurations such as spectroscopy.[2][3]

Overview table

edit
This table does not include uncommon and experimental sequences.

Group Sequence Abbr. Physics Main clinical distinctions Example
Spin echo T1 weighted T1 Measuring spin–lattice relaxation by using a short repetition time (TR) and echo time (TE).

Standard foundation and comparison for other sequences

T2 weighted T2 Measuring spin–spin relaxation by using long TR and TE times
  • Higher signal for more water content[4]
  • Low signal for fat in standard Spine Echo (SE),[4] though not with Fast Spin Echo/Turbo Spin Echo (FSE/TSE). FSE/TSE is the standard of care in modern medicine because it is faster. With FSE/TSE, fat has high signal due to disruption of hyperfine J-coupling between adjacent fat protons.[6]
  • Low signal for paramagnetic substances[5]

Standard foundation and comparison for other sequences

Proton density weighted PD Long TR (to reduce T1) and short TE (to minimize T2).[7] Joint disease and injury.[8]
Gradient echo (GRE) Steady-state free precession SSFP Maintenance of a steady, residual transverse magnetisation over successive cycles.[10] Creation of cardiac MRI videos (pictured).[10]
Effective T2
or "T2-star"		 T2* Spoiled gradient recalled echo (GRE) with a long echo time and small flip angle[11] Low signal from hemosiderin deposits (pictured) and hemorrhages.[11]
Susceptibility-weighted SWI Spoiled gradient recalled echo (GRE), fully flow compensated, long echo time, combines phase image with magnitude image[12] Detecting small amounts of hemorrhage (diffuse axonal injury pictured) or calcium.[12]
Inversion recovery Short tau inversion recovery STIR Fat suppression by setting an inversion time where the signal of fat is zero.[13] High signal in edema, such as in more severe stress fracture.[14] Shin splints pictured:
Fluid-attenuated inversion recovery FLAIR Fluid suppression by setting an inversion time that nulls fluids High signal in lacunar infarction, multiple sclerosis (MS) plaques, subarachnoid haemorrhage and meningitis (pictured).[15]
Double inversion recovery DIR Simultaneous suppression of cerebrospinal fluid and white matter by two inversion times.[16] High signal of multiple sclerosis plaques (pictured).[16]
Diffusion weighted (DWI) Conventional DWI Measure of Brownian motion of water molecules.[17] High signal within minutes of cerebral infarction (pictured).[18]
Apparent diffusion coefficient ADC Reduced T2 weighting by taking multiple conventional DWI images with different DWI weighting, and the change corresponds to diffusion.[19] Low signal minutes after cerebral infarction (pictured).[20]
Diffusion tensor DTI Mainly tractography (pictured) by an overall greater Brownian motion of water molecules in the directions of nerve fibers.[21]
Perfusion weighted (PWI) Dynamic susceptibility contrast DSC Measures changes over time in susceptibility-induced signal loss due to gadolinium contrast injection.[23]
  • Provides measurements of blood flow
  • In cerebral infarction, the infarcted core and the penumbra have decreased perfusion and delayed contrast arrival (pictured).[24]
Arterial spin labelling ASL Magnetic labeling of arterial blood below the imaging slab, which subsequently enters the region of interest.[25] It does not need gadolinium contrast.[26]
Dynamic contrast enhanced DCE Measures changes over time in the shortening of the spin–lattice relaxation (T1) induced by a gadolinium contrast bolus.[27] Faster Gd contrast uptake along with other features is suggestive of malignancy (pictured).[28]
Functional MRI (fMRI) Blood-oxygen-level dependent imaging BOLD Changes in oxygen saturation-dependent magnetism of hemoglobin reflects tissue activity.[29] Localizing brain activity from performing an assigned task (e.g. talking, moving fingers) before surgery, also used in research of cognition.[30]
Magnetic resonance angiography (MRA) and venography Time-of-flight TOF Blood entering the imaged area is not yet magnetically saturated, giving it a much higher signal when using short echo time and flow compensation. Detection of aneurysm, stenosis, or dissection[31]
Phase-contrast magnetic resonance imaging PC-MRA Two gradients with equal magnitude, but opposite direction, are used to encode a phase shift, which is proportional to the velocity of spins.[32] Detection of aneurysm, stenosis, or dissection (pictured).[31]
(VIPR)

Spin echo

[edit]
Main articles: Spin echo and Relaxation (NMR)
Effects of TR and TE on MR signal
Examples of T1-weighted, T2-weighted, and PD-weighted MRI scans

T1 and T2

[edit]

Each tissue returns to its equilibrium state after excitation by the independent relaxation processes of T1 (spin-lattice; that is, magnetization in the same direction as the static magnetic field) and T2 (spin-spin; transverse to the static magnetic field). To create a T1-weighted image, magnetization is allowed to recover before measuring the MR signal by changing the repetition time (TR). This image weighting is useful for assessing the cerebral cortex, identifying fatty tissue, characterizing focal liver lesions, and in general, obtaining morphological information, as well as for post-contrast imaging. To create a T2-weighted image, magnetization is allowed to decay before measuring the MR signal by changing the echo time (TE). This image weighting is useful for detecting edema and inflammation, revealing white matter lesions, and assessing zonal anatomy in the prostate and uterus.

The standard display of MRI images is to represent fluid characteristics in black and white images, where different tissues turn out as follows:

Signal T1-weighted T2-weighted
High
Inter- mediate Grey matter darker than white matter[35] White matter darker than grey matter[35]
Low

Proton density

[edit]
Proton density-weighted image of a knee with synovial chondromatosis

Proton density (PD)- weighted images are created by having a long repetition time (TR) and a short echo time (TE).[36] On images of the brain, this sequence has a more pronounced distinction between grey matter (bright) and white matter (darker grey), but with little contrast between brain and CSF.[36] It is very useful for the detection of arthropathy and injury.[37]

Gradient echo

[edit]
Main article: Gradient echo
Gradient echo sequence[38]

A gradient echo sequence does not use a 180 degrees RF pulse to make the spins of particles coherent. Instead, it uses magnetic gradients to manipulate the spins, allowing the spins to dephase and rephase when required. After an excitation pulse, the spins are dephased, no signal is produced because the spins are not coherent. When the spins are rephased, they become coherent, and thus signal (or "echo") is generated to form images. Unlike spin echo, gradient echo does not need to wait for transverse magnetisation to decay completely before initiating another sequence, thus it requires very short repetition times (TR), and therefore to acquire images in a short time. After echo is formed, some transverse magnetisations remains. Manipulating gradients during this time will produce images with different contrast. There are three main methods of manipulating contrast at this stage, namely steady-state free-precession (SSFP) that does not spoil the remaining transverse magnetisation, but attempts to recover them (thus producing T2-weighted images); the sequence with spoiler gradient that averages the transverse magnetisations (thus producing mixed T1 and T2-weighted images), and RF spoiler that vary the phases of RF pulse to eliminates the transverse magnetisation, thus producing pure T1-weighted images.[39]

For comparison purposes, the repetition time of a gradient echo sequence is of the order of 3 milliseconds, versus about 30 ms of a spin echo sequence.[citation needed]

Inversion recovery

[edit]
Main article: Inversion recovery

Inversion recovery is an MRI sequence that provides high contrast between tissue and lesion. It can be used to provide high T1 weighted image, high T2 weighted image, and to suppress the signals from fat, blood, or cerebrospinal fluid (CSF).[40]

Diffusion weighted

[edit]
Main article: Diffusion MRI
DTI image

Diffusion MRI measures the diffusion of water molecules in biological tissues.[41] Clinically, diffusion MRI is useful for the diagnoses of conditions (e.g., stroke) or neurological disorders (e.g., multiple sclerosis), and helps better understand the connectivity of white matter axons in the central nervous system.[42] In an isotropic medium (inside a glass of water for example), water molecules naturally move randomly according to turbulence and Brownian motion. In biological tissues however, where the Reynolds number is low enough for laminar flow, the diffusion may be anisotropic. For example, a molecule inside the axon of a neuron has a low probability of crossing the myelin membrane. Therefore, the molecule moves principally along the axis of the neural fiber. If it is known that molecules in a particular voxel diffuse principally in one direction, the assumption can be made that the majority of the fibers in this area are parallel to that direction.

The recent development of diffusion tensor imaging (DTI)[43] enables diffusion to be measured in multiple directions, and the fractional anisotropy in each direction to be calculated for each voxel. This enables researchers to make brain maps of fiber directions to examine the connectivity of different regions in the brain (using tractography) or to examine areas of neural degeneration and demyelination in diseases like multiple sclerosis.

Another application of diffusion MRI is diffusion-weighted imaging (DWI). Following an ischemic stroke, DWI is highly sensitive to the changes occurring in the lesion.[44] It is speculated that increases in restriction (barriers) to water diffusion, as a result of cytotoxic edema (cellular swelling), is responsible for the increase in signal on a DWI scan. The DWI enhancement appears within 5–10 minutes of the onset of stroke symptoms (as compared to computed tomography, which often does not detect changes of acute infarct for up to 4–6 hours) and remains for up to two weeks. Coupled with imaging of cerebral perfusion, researchers can highlight regions of "perfusion/diffusion mismatch" that may indicate regions capable of salvage by reperfusion therapy.

Like many other specialized applications, this technique is usually coupled with a fast image acquisition sequence, such as echo planar imaging sequence.

Perfusion weighted

[edit]
MRI perfusion showing a delayed time-to-maximum flow (Tmax) in the penumbra in a case of occlusion of the left middle cerebral artery.
Main article: Perfusion MRI

Perfusion-weighted imaging (PWI) is performed by 3 main techniques:

  • Dynamic susceptibility contrast (DSC): Gadolinium contrast is injected, and rapid repeated imaging (generally gradient-echo echo-planar T2 weighted) quantifies susceptibility-induced signal loss.[45]
  • Dynamic contrast enhanced (DCE): Measuring shortening of the spin–lattice relaxation (T1) induced by a gadolinium contrast bolus.[46]
  • Arterial spin labelling (ASL): Magnetic labeling of arterial blood below the imaging slab, without the need of gadolinium contrast.[47]

The acquired data is then postprocessed to obtain perfusion maps with different parameters, such as BV (blood volume), BF (blood flow), MTT (mean transit time) and TTP (time to peak).

In cerebral infarction, the penumbra has decreased perfusion.[24] Another MRI sequence, diffusion-weighted MRI, estimates the amount of tissue that is already necrotic, and the combination of those sequences can therefore be used to estimate the amount of brain tissue that is salvageable by thrombolysis and/or thrombectomy.

Functional MRI

[edit]
Main article: Functional MRI
A fMRI scan showing regions of activation in orange, including the primary visual cortex (V1, BA17)

Functional MRI (fMRI) measures signal changes in the brain that are due to changing neural activity. It is used to understand how different parts of the brain respond to external stimuli or passive activity in a resting state, and has applications in behavioral and cognitive research, and in planning neurosurgery of eloquent brain areas.[48][49] Researchers use statistical methods to construct a 3-D parametric map of the brain indicating the regions of the cortex that demonstrate a significant change in activity in response to the task. Compared to anatomical T1W imaging, the brain is scanned at lower spatial resolution but at a higher temporal resolution (typically once every 2–3 seconds). Increases in neural activity cause changes in the MR signal via T*
2 changes;[50] this mechanism is referred to as the BOLD (blood-oxygen-level dependent) effect. Increased neural activity causes an increased demand for oxygen, and the vascular system actually overcompensates for this, increasing the amount of oxygenated hemoglobin relative to deoxygenated hemoglobin. Because deoxygenated hemoglobin attenuates the MR signal, the vascular response leads to a signal increase that is related to the neural activity. The precise nature of the relationship between neural activity and the BOLD signal is a subject of current research. The BOLD effect also allows for the generation of high resolution 3D maps of the venous vasculature within neural tissue.

While BOLD signal analysis is the most common method employed for neuroscience studies in human subjects, the flexible nature of MR imaging provides means to sensitize the signal to other aspects of the blood supply. Alternative techniques employ arterial spin labeling (ASL) or weighting the MRI signal by cerebral blood flow (CBF) and cerebral blood volume (CBV). The CBV method requires injection of a class of MRI contrast agents that are now in human clinical trials. Because this method has been shown to be far more sensitive than the BOLD technique in preclinical studies, it may potentially expand the role of fMRI in clinical applications. The CBF method provides more quantitative information than the BOLD signal, albeit at a significant loss of detection sensitivity.[citation needed]

Magnetic resonance angiography

[edit]
Time-of-flight MRA at the level of the Circle of Willis.
Main article: Magnetic resonance angiography

Magnetic resonance angiography (MRA) is a group of techniques based to image blood vessels. Magnetic resonance angiography is used to generate images of arteries (and less commonly veins) in order to evaluate them for stenosis (abnormal narrowing), occlusions, aneurysms (vessel wall dilatations, at risk of rupture) or other abnormalities. MRA is often used to evaluate the arteries of the neck and brain, the thoracic and abdominal aorta, the renal arteries, and the legs (the latter exam is often referred to as a "run-off").

Phase contrast

[edit]
Main article: Phase contrast magnetic resonance imaging

Phase contrast MRI (PC-MRI) is used to measure flow velocities in the body. It is used mainly to measure blood flow in the heart and throughout the body. PC-MRI may be considered a method of magnetic resonance velocimetry. Since modern PC-MRI typically is time-resolved, it also may be referred to as 4-D imaging (three spatial dimensions plus time).[51]

Susceptibility weighted imaging

[edit]
Main article: Susceptibility weighted imaging

Susceptibility-weighted imaging (SWI) is a new type of contrast in MRI different from spin density, T1, or T2 imaging. This method exploits the susceptibility differences between tissues and uses a fully velocity-compensated, three-dimensional, RF-spoiled, high-resolution, 3D-gradient echo scan. This special data acquisition and image processing produces an enhanced contrast magnitude image very sensitive to venous blood, hemorrhage and iron storage. It is used to enhance the detection and diagnosis of tumors, vascular and neurovascular diseases (stroke and hemorrhage), multiple sclerosis,[52] Alzheimer's, and also detects traumatic brain injuries that may not be diagnosed using other methods.[53]

Magnetization transfer

[edit]
Main article: Magnetization transfer

Magnetization transfer (MT) is a technique to enhance image contrast in certain applications of MRI.

Bound protons are associated with proteins and as they have a very short T2 decay they do not normally contribute to image contrast. However, because these protons have a broad resonance peak they can be excited by a radiofrequency pulse that has no effect on free protons. Their excitation increases image contrast by transfer of saturated spins from the bound pool into the free pool, thereby reducing the signal of free water. This homonuclear magnetization transfer provides an indirect measurement of macromolecular content in tissue. Implementation of homonuclear magnetization transfer involves choosing suitable frequency offsets and pulse shapes to saturate the bound spins sufficiently strongly, within the safety limits of specific absorption rate for MRI.[54]

The most common use of this technique is for suppression of background signal in time of flight MR angiography.[55] There are also applications in neuroimaging particularly in the characterization of white matter lesions in multiple sclerosis.[56]

Fat suppression

[edit]
Main article: Fat suppression

Fat suppression is useful for example to distinguish active inflammation in the intestines from fat deposition such as can be caused by long-standing (but possibly inactive) inflammatory bowel disease, but also obesity, chemotherapy and celiac disease.[57] Without fat suppression techniques, fat and fluid will have similar signal intensities on fast spin-echo sequences.[58]

Techniques to suppress fat on MRI mainly include:[59]

  • Identifying fat by the chemical shift of its atoms, causing different time-dependent phase shifts compared to water.
  • Frequency-selective saturation of the spectral peak of fat by a "fat sat" pulse before imaging.
  • Short tau inversion recovery (STIR), a T1-dependent method
  • Spectral presaturation with inversion recovery (SPIR)

Neuromelanin imaging

[edit]

This method exploits the paramagnetic properties of neuromelanin and can be used to visualize the substantia nigra and the locus coeruleus. It is used to detect the atrophy of these nuclei in Parkinson's disease and other parkinsonisms, and also detects signal intensity changes in major depressive disorder and schizophrenia.[60]

Uncommon and experimental sequences

[edit]

The following sequences are not commonly used clinically, and/or are at an experimental stage.

T1 rho (T1ρ)

[edit]

T1 rho (T1ρ) is an experimental MRI sequence that may be used in musculoskeletal imaging. It does not yet have widespread use.[61]

Molecules have a kinetic energy that is a function of the temperature and is expressed as translational and rotational motions, and by collisions between molecules. The moving dipoles disturb the magnetic field but are often extremely rapid so that the average effect over a long time-scale may be zero. However, depending on the time-scale, the interactions between the dipoles do not always average away. At the slowest extreme the interaction time is effectively infinite and occurs where there are large, stationary field disturbances (e.g., a metallic implant). In this case the loss of coherence is described as a "static dephasing". T2* is a measure of the loss of coherence in an ensemble of spins that includes all interactions (including static dephasing). T2 is a measure of the loss of coherence that excludes static dephasing, using an RF pulse to reverse the slowest types of dipolar interaction. There is in fact a continuum of interaction time-scales in a given biological sample, and the properties of the refocusing RF pulse can be tuned to refocus more than just static dephasing. In general, the rate of decay of an ensemble of spins is a function of the interaction times and also the power of the RF pulse. This type of decay, occurring under the influence of RF, is known as T1ρ. It is similar to T2 decay but with some slower dipolar interactions refocused, as well as static interactions, hence T1ρ≥T2.[62]

Others

[edit]
  • Saturation recovery sequences are rarely used, but can measure spin-lattice relaxation time (T1) more quickly than an inversion recovery pulse sequence.[63]
  • Double-oscillating-diffusion-encoding (DODE) and double diffusion encoding (DDE) imaging are specific forms of MRI diffusion imaging, which can be used to measure diameters and lengths of axon pores.[64]

References

[edit]
  1. ^ Jones J, Gaillard F. "MRI sequences (overview)". Radiopaedia. Retrieved 2017-10-15.
  2. ^ Marino MA, Helbich T, Baltzer P, Pinker-Domenig K (February 2018). "Multiparametric MRI of the breast: A review". Journal of Magnetic Resonance Imaging. 47 (2): 301–315. doi:10.1002/jmri.25790. PMID 28639300. S2CID 206108382.
  3. ^ Tahmassebi A, Wengert GJ, Helbich TH, Bago-Horvath Z, Alaei S, Bartsch R, et al. (February 2019). "Impact of Machine Learning With Multiparametric Magnetic Resonance Imaging of the Breast for Early Prediction of Response to Neoadjuvant Chemotherapy and Survival Outcomes in Breast Cancer Patients". Investigative Radiology. 54 (2): 110–117. doi:10.1097/RLI.0000000000000518. PMC 6310100. PMID 30358693.
  4. ^ a b c d "Magnetic Resonance Imaging". University of Wisconsin. Archived from the original on 2017-05-10. Retrieved 2016-03-14.
  5. ^ a b c d Johnson KA. "Basic proton MR imaging. Tissue Signal Characteristics". Harvard Medical School. Archived from the original on 2016-03-05. Retrieved 2016-03-14.
  6. ^ Henkelman, RM; Hardy, PA; Bishop, JE; Poon, CS; Plewes, DB (September 1992). "Why fat is bright in RARE and fast spin-echo imaging". Journal of magnetic resonance imaging : JMRI. 2 (5): 533–40. doi:10.1002/jmri.1880020511. PMID 1392246.
  7. ^ Graham D, Cloke P, Vosper M (2011-05-31). Principles and Applications of Radiological Physics E-Book (6 ed.). Elsevier Health Sciences. p. 292. ISBN 978-0-7020-4614-8.}
  8. ^ du Plessis V, Jones J. "MRI sequences (overview)". Radiopaedia. Retrieved 2017-01-13.
  9. ^ Lefevre N, Naouri JF, Herman S, Gerometta A, Klouche S, Bohu Y (2016). "A Current Review of the Meniscus Imaging: Proposition of a Useful Tool for Its Radiologic Analysis". Radiology Research and Practice. 2016: 8329296. doi:10.1155/2016/8329296. PMC 4766355. PMID 27057352.
  10. ^ a b Luijkx T, Weerakkody Y. "Steady-state free precession MRI". Radiopaedia. Retrieved 2017-10-13.
  11. ^ a b Chavhan GB, Babyn PS, Thomas B, Shroff MM, Haacke EM (2009). "Principles, techniques, and applications of T2*-based MR imaging and its special applications". Radiographics. 29 (5): 1433–49. doi:10.1148/rg.295095034. PMC 2799958. PMID 19755604.
  12. ^ a b Di Muzio B, Gaillard F. "Susceptibility weighted imaging". Retrieved 2017-10-15.
  13. ^ Sharma R, Taghi Niknejad M. "Short tau inversion recovery". Radiopaedia. Retrieved 2017-10-13.
  14. ^ Berger F, de Jonge M, Smithuis R, Maas M. "Stress fractures". Radiology Assistant. Radiology Society of the Netherlands. Retrieved 2017-10-13.
  15. ^ Hacking C, Taghi Niknejad M, et al. "Fluid attenuation inversion recoveryg". radiopaedia.org. Retrieved 2015-12-03.
  16. ^ a b Di Muzio B, Abd Rabou A. "Double inversion recovery sequence". Radiopaedia. Retrieved 2017-10-13.
  17. ^ Lee M, Bashir U. "Diffusion weighted imaging". Radiopaedia. Retrieved 2017-10-13.
  18. ^ Weerakkody Y, Gaillard F. "Ischaemic stroke". Radiopaedia. Retrieved 2017-10-15.
  19. ^ Hammer M. "MRI Physics: Diffusion-Weighted Imaging". XRayPhysics. Retrieved 2017-10-15.
  20. ^ An H, Ford AL, Vo K, Powers WJ, Lee JM, Lin W (May 2011). "Signal evolution and infarction risk for apparent diffusion coefficient lesions in acute ischemic stroke are both time- and perfusion-dependent". Stroke. 42 (5): 1276–81. doi:10.1161/STROKEAHA.110.610501. PMC 3384724. PMID 21454821.
  21. ^ a b Smith D, Bashir U. "Diffusion tensor imaging". Radiopaedia. Retrieved 2017-10-13.
  22. ^ Chua TC, Wen W, Slavin MJ, Sachdev PS (February 2008). "Diffusion tensor imaging in mild cognitive impairment and Alzheimer's disease: a review". Current Opinion in Neurology. 21 (1): 83–92. doi:10.1097/WCO.0b013e3282f4594b. PMID 18180656. S2CID 24731783.
  23. ^ Gaillard F. "Dynamic susceptibility contrast (DSC) MR perfusion". Radiopaedia. Retrieved 2017-10-14.
  24. ^ a b Chen F, Ni YC (March 2012). "Magnetic resonance diffusion-perfusion mismatch in acute ischemic stroke: An update". World Journal of Radiology. 4 (3): 63–74. doi:10.4329/wjr.v4.i3.63. PMC 3314930. PMID 22468186.
  25. ^ "Arterial spin labeling". University of Michigan. Retrieved 2017-10-27.
  26. ^ Gaillard F. "Arterial spin labelling (ASL) MR perfusion". Radiopaedia. Retrieved 2017-10-15.
  27. ^ Gaillard F. "Dynamic contrast enhanced (DCE) MR perfusion". Radiopaedia. Retrieved 2017-10-15.
  28. ^ Turnbull LW (January 2009). "Dynamic contrast-enhanced MRI in the diagnosis and management of breast cancer". NMR in Biomedicine. 22 (1): 28–39. doi:10.1002/nbm.1273. PMID 18654999. S2CID 5305422.
  29. ^ Chou Ih. "Milestone 19: (1990) Functional MRI". Nature. Retrieved 9 August 2013.
  30. ^ Luijkx T, Gaillard F. "Functional MRI". Radiopaedia. Retrieved 2017-10-16.
  31. ^ a b "Magnetic Resonance Angiography (MRA)". Johns Hopkins Hospital. Retrieved 2017-10-15.
  32. ^ Keshavamurthy J, Ballinger R et al. "Phase contrast imaging". Radiopaedia. Retrieved 2017-10-15.
  33. ^ a b c d e f g h "Magnetic Resonance Imaging". University of Wisconsin. Archived from the original on 2017-05-10. Retrieved 2016-03-14.
  34. ^ a b c d e f g h i j k l m n Johnson KA. "Basic proton MR imaging. Tissue Signal Characteristics". Harvard Medical School. Archived from the original on 2016-03-05. Retrieved 2016-03-14.
  35. ^ a b Patil T (2013-01-18). "MRI sequences". Retrieved 2016-03-14.
  36. ^ a b "Structural MRI Imaging". UC San Diego School of Medicine. Retrieved 2017-01-01.
  37. ^ Jones J, Gaillard F. "MRI sequences (overview)". Radiopaedia. Retrieved 2017-01-13.
  38. ^ Gebker R, Schwitter J, Fleck E, Nagel E (2007). "How we perform myocardial perfusion with cardiovascular magnetic resonance". Journal of Cardiovascular Magnetic Resonance. 9 (3): 539–547. CiteSeerX 10.1.1.655.7675. doi:10.1080/10976640600897286. PMID 17365233.
  39. ^ Hargreaves BA (December 2012). "Rapid gradient-echo imaging". Journal of Magnetic Resonance Imaging. 36 (6): 1300–1313. doi:10.1002/jmri.23742. PMC 3502662. PMID 23097185.
  40. ^ Bydder GM, Hajnal JV, Young IR (March 1998). "MRI: use of the inversion recovery pulse sequence". Clinical Radiology. 53 (3): 159–76. doi:10.1016/s0009-9260(98)80096-2. PMID 9528866.
  41. ^ Le Bihan D, Breton E, Lallemand D, Grenier P, Cabanis E, Laval-Jeantet M (November 1986). "MR imaging of intravoxel incoherent motions: application to diffusion and perfusion in neurologic disorders". Radiology. 161 (2): 401–407. doi:10.1148/radiology.161.2.3763909. PMID 3763909. S2CID 14420005.
  42. ^ "Diffusion Inaging". Stanford University. Archived from the original on 24 December 2011. Retrieved 28 April 2012.
  43. ^ Filler A (2009). "The History, Development and Impact of Computed Imaging in Neurological Diagnosis and Neurosurgery: CT, MRI, and DTI". Nature Precedings. doi:10.1038/npre.2009.3267.4.
  44. ^ Moseley ME, Cohen Y, Mintorovitch J, Chileuitt L, Shimizu H, Kucharczyk J, et al. (May 1990). "Early detection of regional cerebral ischemia in cats: comparison of diffusion- and T2-weighted MRI and spectroscopy". Magnetic Resonance in Medicine. 14 (2): 330–346. doi:10.1002/mrm.1910140218. PMID 2345513. S2CID 23754356.
  45. ^ Gaillard F. "Dynamic susceptibility contrast (DSC) MR perfusion". Radiopaedia. Retrieved 2017-10-14.
  46. ^ Gaillard F, Goel A, Murphy A. "Dynamic contrast enhanced (DCE) MR perfusion". Radiopaedia. Retrieved 2017-10-15.
  47. ^ Gaillard F. "Arterial spin labelling (ASL) MR perfusion". Radiopaedia. Retrieved 2017-10-15.
  48. ^ Heeger DJ, Ress D (February 2002). "What does fMRI tell us about neuronal activity?". Nature Reviews. Neuroscience. 3 (2): 142–151. doi:10.1038/nrn730. PMID 11836522. S2CID 7132655.
  49. ^ Giussani C, Roux FE, Ojemann J, Sganzerla EP, Pirillo D, Papagno C (January 2010). "Is preoperative functional magnetic resonance imaging reliable for language areas mapping in brain tumor surgery? Review of language functional magnetic resonance imaging and direct cortical stimulation correlation studies". Neurosurgery. 66 (1): 113–120. doi:10.1227/01.NEU.0000360392.15450.C9. PMID 19935438. S2CID 207142804.
  50. ^ Thulborn KR, Waterton JC, Matthews PM, Radda GK (February 1982). "Oxygenation dependence of the transverse relaxation time of water protons in whole blood at high field". Biochimica et Biophysica Acta (BBA) - General Subjects. 714 (2): 265–270. doi:10.1016/0304-4165(82)90333-6. PMID 6275909.
  51. ^ Stankovic Z, Allen BD, Garcia J, Jarvis KB, Markl M (April 2014). "4D flow imaging with MRI". Cardiovascular Diagnosis and Therapy. 4 (2): 173–192. doi:10.3978/j.issn.2223-3652.2014.01.02. PMC 3996243. PMID 24834414.
  52. ^ Wiggermann V, Hernández Torres E, Vavasour IM, Moore GR, Laule C, MacKay AL, et al. (July 2013). "Magnetic resonance frequency shifts during acute MS lesion formation". Neurology. 81 (3): 211–218. doi:10.1212/WNL.0b013e31829bfd63. PMC 3770162. PMID 23761621.
  53. ^ Reichenbach JR, Venkatesan R, Schillinger DJ, Kido DK, Haacke EM (July 1997). "Small vessels in the human brain: MR venography with deoxyhemoglobin as an intrinsic contrast agent". Radiology. 204 (1): 272–277. doi:10.1148/radiology.204.1.9205259. PMID 9205259.[permanent dead link‍]
  54. ^ McRobbie DW (2007). MRI from picture to proton. Cambridge, UK; New York: Cambridge University Press. ISBN 978-0-521-68384-5.
  55. ^ Wheaton AJ, Miyazaki M (August 2012). "Non-contrast enhanced MR angiography: physical principles". Journal of Magnetic Resonance Imaging. 36 (2): 286–304. doi:10.1002/jmri.23641. PMID 22807222. S2CID 24048799.
  56. ^ Filippi M, Rocca MA, De Stefano N, Enzinger C, Fisher E, Horsfield MA, et al. (December 2011). "Magnetic resonance techniques in multiple sclerosis: the present and the future". Archives of Neurology. 68 (12): 1514–1520. doi:10.1001/archneurol.2011.914. PMID 22159052.
  57. ^ Gore R, Smithuis R (2014-05-21). "Bowel wall thickening – CT-pattern – Type 4 – Fat target sign". Radiology Assistant. Retrieved 2017-09-27.
  58. ^ Bloem JL, Reijnierse M, Huizinga TW, van der Helm-van Mil AH (June 2018). "MR signal intensity: staying on the bright side in MR image interpretation". RMD Open. 4 (1): e000728. doi:10.1136/rmdopen-2018-000728. PMC 6018882. PMID 29955387.
  59. ^ Weishaupt D, Koechli VD, Marincek B (2008). "Chapter 9: Fast Suppression Techniques". How does MRI work?: An Introduction to the Physics and Function of Magnetic Resonance Imaging (2nd ed.). Springer Science & Business Media. p. 70. ISBN 978-3-540-37845-7.
  60. ^ Sasaki M, Shibata E, Tohyama K, Takahashi J, Otsuka K, Tsuchiya K, et al. (July 2006). "Neuromelanin magnetic resonance imaging of locus ceruleus and substantia nigra in Parkinson's disease". NeuroReport. 17 (11): 1215–1218. doi:10.1097/01.wnr.0000227984.84927.a7. PMID 16837857. S2CID 24597825.
  61. ^ Luijkx T, Morgan MA. "T1 rho". Radiopaedia. Retrieved 2017-10-15.
  62. ^ Borthakur A, Mellon E, Niyogi S, Witschey W, Kneeland JB, Reddy R (November 2006). "Sodium and T1rho MRI for molecular and diagnostic imaging of articular cartilage". NMR in Biomedicine. 19 (7): 781–821. doi:10.1002/nbm.1102. PMC 2896046. PMID 17075961.
  63. ^ Jones J, Ballinger JR. "Saturation recovery sequences". Radiopaedia. Retrieved 2017-10-15.
  64. ^ Andrada I, Ivana D, Noam S, Daniel A (2016). "Advanced diffusion MRI for microstructure imaging". Frontiers in Physics. 4. doi:10.3389/conf.FPHY.2016.01.00001.
Retrieved from "https://en.wikipedia.org/w/index.php?title=MRI_pulse_sequence&oldid=1256077778#GRE"