Magnetic resonance imaging is a medical imaging technique used in radiology to form pictures of the anatomy and the physiological processes of the body in both health and disease. MRI scanners use strong magnetic fields, electric field gradients, and radio waves to generate images of the organs in the body. MRI does not involve X-rays and the use of ionizing radiation, which distinguishes it from CT or CAT scans. Magnetic resonance imaging is a medical application of nuclear magnetic resonance (NMR). NMR can also be used for imaging in other NMR applications such as NMR spectroscopy.

While the hazards of X-rays are now well-controlled in most medical contexts, MRI may still be seen as a better choice than CT. MRI is widely used in hospitals and clinics for medical diagnosis, staging of disease and follow-up without exposing the body to radiation. However, MRI may often yield different diagnostic information compared with CT. There may be risks and discomfort associated with MRI scans. Compared with CT scans, MRI scans typically take longer and are louder, and they usually need the subject to enter a narrow, confining tube. In addition, people with some medical implants or other non-removable metal inside the body may be unable to undergo an MRI examination safely.

MRI was originally called 'NMRI' (nuclear magnetic resonance imaging) and is a form of NMR, though the use of 'nuclear' in the acronym was dropped to avoid negative associations with the word.[1] Certain atomic nuclei are able to absorb and emit radio frequency energy when placed in an external magnetic field. In clinical and research MRI, hydrogen atoms are most often used to generate a detectable radio-frequency signal that is received by antennas in close proximity to the anatomy being examined. Hydrogen atoms are naturally abundant in people and other biological organisms, particularly in water and fat. For this reason, most MRI scans essentially map the location of water and fat in the body. Pulses of radio waves excite the nuclear spin energy transition, and magnetic field gradients localize the signal in space. By varying the parameters of the pulse sequence, different contrasts may be generated between tissues based on the relaxation properties of the hydrogen atoms therein.

Since its development in the 1970s and 1980s, MRI has proven to be a highly versatile imaging technique. While MRI is most prominently used in diagnostic medicine and biomedical research, it also may be used to form images of non-living objects. MRI scans are capable of producing a variety of chemical and physical data, in addition to detailed spatial images. The sustained increase in demand for MRI within health systems has led to concerns about cost effectiveness and overdiagnosis.[2][3]


Construction and physics

Schematic of construction of a cylindrical superconducting MR scanner.

To perform a study, the person is positioned within an MRI scanner that forms a strong magnetic field around the area to be imaged. In most medical applications, protons (hydrogen atoms) in tissues containing water molecules create a signal that is processed to form an image of the body. First, energy from an oscillating magnetic field temporarily is applied to the patient at the appropriate resonance frequency. The excited hydrogen atoms emit a radio frequency signal, which is measured by a receiving coil. The radio signal may be made to encode position information by varying the main magnetic field using gradient coils. As these coils are rapidly switched on and off they create the characteristic repetitive noise of an MRI scan. The contrast between different tissues is determined by the rate at which excited atoms return to the equilibrium state. Exogenous contrast agents may be given to the person to make the image clearer.[4]

The major components of an MRI scanner are: the main magnet, which polarizes the sample, the shim coils for correcting shifts in the homogeneity of the main magnetic field, the gradient system which is used to localize the MR signal and the RF system, which excites the sample and detects the resulting NMR signal. The whole system is controlled by one or more computers.

MRI requires a magnetic field that is both strong and uniform. The field strength of the magnet is measured in teslas – and while the majority of systems operate at 1.5 T, commercial systems are available between 0.2 and 7 T. Most clinical magnets are superconducting magnets, which require liquid helium. Lower field strengths can be achieved with permanent magnets, which are often used in "open" MRI scanners for claustrophobic patients.[5] Recently, MRI has been demonstrated also at ultra-low fields, i.e., in the microtesla-to-millitesla range, where sufficient signal quality is made possible by prepolarization (on the order of 10-100 mT) and by measuring the Larmor precession fields at about 100 microtesla with highly sensitive superconducting quantum interference devices (SQUIDs).[6][7][8]

T1 and T2

Effects of TR and TE on MR signal
Examples of T1 weighted, T2 weighted and PD weighted MRI scans

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 for 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
Inter- mediate Gray matter darker than white matter[11] White matter darker than grey matter[11]


Usage by organ or system

Patient being positioned for MR study of the head and abdomen.

MRI has a wide range of applications in medical diagnosis and more than 25,000 scanners are estimated to be in use worldwide.[12] MRI affects diagnosis and treatment in many specialties although the effect on improved health outcomes is uncertain.[13]

MRI is the investigation of choice in the preoperative staging of rectal and prostate cancer and, has a role in the diagnosis, staging, and follow-up of other tumors.[14]


MRI image of white matter tracts

MRI is the investigative tool of choice for neurological cancers, as it has better resolution than CT and offers better visualization of the posterior fossa. The contrast provided between grey and white matter makes MRI the best choice for many conditions of the central nervous system, including demyelinating diseases, dementia, cerebrovascular disease, infectious diseases, and epilepsy.[15] Since many images are taken milliseconds apart, it shows how the brain responds to different stimuli, enabling researchers to study both the functional and structural brain abnormalities in psychological disorders.[16] MRI also is used in guided stereotactic surgery and radiosurgery for treatment of intracranial tumors, arteriovenous malformations, and other surgically treatable conditions using a device known as the N-localizer.[17][18][19]


MR angiogram in congenital heart disease

Cardiac MRI is complementary to other imaging techniques, such as echocardiography, cardiac CT, and nuclear medicine. Its applications include assessment of myocardial ischemia and viability, cardiomyopathies, myocarditis, iron overload, vascular diseases, and congenital heart disease.[20]


Applications in the musculoskeletal system include spinal imaging, assessment of joint disease, and soft tissue tumors.[21]

Liver and gastrointestinal

Hepatobiliary MR is used to detect and characterize lesions of the liver, pancreas, and bile ducts. Focal or diffuse disorders of the liver may be evaluated using diffusion-weighted, opposed-phase imaging, and dynamic contrast enhancement sequences. Extracellular contrast agents are used widely in liver MRI and newer hepatobiliary contrast agents also provide the opportunity to perform functional biliary imaging. Anatomical imaging of the bile ducts is achieved by using a heavily T2-weighted sequence in magnetic resonance cholangiopancreatography (MRCP). Functional imaging of the pancreas is performed following administration of secretin. MR enterography provides non-invasive assessment of inflammatory bowel disease and small bowel tumors. MR-colonography may play a role in the detection of large polyps in patients at increased risk of colorectal cancer.[22][23][24][25]


Magnetic resonance angiography

Magnetic resonance angiography (MRA) generates pictures of the arteries to evaluate them for stenosis (abnormal narrowing) or aneurysms (vessel wall dilatations, at risk of rupture). MRA is often used to evaluate the arteries of the neck and brain, the thoracic and abdominal aorta, the renal arteries, and the legs (called a "run-off"). A variety of techniques can be used to generate the pictures, such as administration of a paramagnetic contrast agent (gadolinium) or using a technique known as "flow-related enhancement" (e.g., 2D and 3D time-of-flight sequences), where most of the signal on an image is due to blood that recently moved into that plane (see also FLASH MRI). Techniques involving phase accumulation (known as phase contrast angiography) can also be used to generate flow velocity maps easily and accurately. Magnetic resonance venography (MRV) is a similar procedure that is used to image veins. In this method, the tissue is now excited inferiorly, while the signal is gathered in the plane immediately superior to the excitation plane—thus imaging the venous blood that recently moved from the excited plane.[26]

Contrast agents

MRI for imaging anatomical structures or blood flow do not require contrast agents as the varying properties of the tissues or blood provide natural contrasts. However, for more specific types of imaging, exogenous contrast agents may be given intravenously, orally, or intra-articularly.[4] The most commonly used intravenous contrast agents are based on chelates of gadolinium.[27] In general, these agents have proved safer than the iodinated contrast agents used in X-ray radiography or CT. Anaphylactoid reactions are rare, occurring in approx. 0.03–0.1%.[28] Of particular interest is the lower incidence of nephrotoxicity, compared with iodinated agents, when given at usual doses—this has made contrast-enhanced MRI scanning an option for patients with renal impairment, who would otherwise not be able to undergo contrast-enhanced CT.[29]

Although gadolinium agents have proved useful for patients with renal impairment, in patients with severe renal failure requiring dialysis there is a risk of a rare but serious illness, nephrogenic systemic fibrosis, which may be linked to the use of certain gadolinium-containing agents. The most frequently linked is gadodiamide, but other agents have been linked too.[30] Although a causal link has not been definitively established, current guidelines in the United States are that dialysis patients should only receive gadolinium agents where essential, and that dialysis should be performed as soon as possible after the scan to remove the agent from the body promptly.[31][32] In Europe, where more gadolinium-containing agents are available, a classification of agents according to potential risks has been released.[33][34] Recently, a new contrast agent named gadoxetate, brand name Eovist (US) or Primovist (EU), was approved for diagnostic use: this has the theoretical benefit of a dual excretion path.[35]


An MRI sequence is a particular setting of radiofrequency pulses and gradients, resulting in a particular image appearance.[36] The T1 and T2 weighting can also be described as MRI sequences.

Overview table

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.

Standard foundation and comparison for other sequences.

Normal axial T2-weighted MR image of the brain.jpg
Proton density weighted PD Long TR (to reduce T1) and short TE (to minimize T2)[37] Joint disease and injury.[38] Proton density MRI of a grade 2 medial meniscal tear.jpg
Gradient echo Steady-state free precession SSFP Maintenance of a steady, residual transverse magnetisation over successive cycles.[40] Creation of cardiac MRI videos (pictured).[40] Four chamber cardiovascular magnetic resonance imaging.gif
Inversion recovery Short tau inversion recovery STIR Fat suppression by setting an inversion time where the signal of fat is zero.[41] High signal in edema, such as in more severe stress fracture.[42] Shin splints pictured: Shinsplint-mri (crop).jpg
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).[43] FLAIR MRI of meningitis.jpg
Double inversion recovery DIR Simultaneous suppression of cerebrospinal fluid and white matter by two inversion times.[44] High signal of multiple sclerosis plaques (pictured).[44] Axial DIR MRI of a brain with multiple sclerosis lesions.jpg
Diffusion weighted (DWI) Conventional DWI Measure of Brownian motion of water molecules.[45] High signal within minutes of cerebral infarction (pictured).[46] Cerebral infarction after 4 hours on DWI MRI.jpg
Apparent diffusion coefficient ADC Reduced T2 weighting by taking multiple conventional DWI images with different DWI weighting, and the change corresponds to diffusion.[47] Low signal minutes after cerebral infarction (pictured).[48] Cerebral infarction after 4 hours on ADC MRI.jpg
Diffusion tensor DTI Mainly tractography (pictured) by an overall greater Brownian motion of water molecules in the directions of nerve fibers.[49] White Matter Connections Obtained with MRI Tractography.png
Perfusion weighted (PWI) Dynamic susceptibility contrast DSC Gadolinium contrast is injected, and rapid repeated imaging (generally gradient-echo echo-planar T2 weighted) quantifies susceptibility-induced signal loss.[51] In cerebral infarction, the infarcted core and the penumbra have decreased perfusion (pictured).[52] Tmax by MRI perfusion in cerebral artery occlusion.jpg
Dynamic contrast enhanced DCE Measuring shortening of the spin–lattice relaxation (T1) induced by a gadolinium contrast bolus.[53]
Arterial spin labelling ASL Magnetic labeling of arterial blood below the imaging slab, which subsequently enters the region of interest.[54] It does not need gadolinium contrast.[55]
Functional MRI (fMRI) Blood-oxygen-level dependent imaging BOLD Changes in oxygen saturation-dependent magnetism of hemoglobin reflects tissue activity.[56] Localizing highly active brain areas before surgery.[57] 1206 FMRI.jpg
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.[58] Mra-mip.jpg
Phase-contrast MRA 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.[59] Detection of aneurysm, stenosis or dissection (pictured).[58] Vastly undersampled Isotropic Projection Reconstruction (VIPR) Phase Contrast (PC) sequence MRI of arterial dissections.jpg
Susceptibility weighted SWI Sensitive for blood and calcium, by a fully flow compensated, long echo, gradient recalled echo (GRE) pulse sequence to exploit magnetic susceptibility differences between tissues. Detecting small amounts of hemorrhage (diffuse axonal injury pictured) or calcium.[60] Susceptibility weighted imaging (SWI) in diffuse axonal injury.jpg

Other specialized configurations

Magnetic resonance spectroscopy

Magnetic resonance spectroscopy (MRS) is used to measure the levels of different metabolites in body tissues. The MR signal produces a spectrum of resonances that corresponds to different molecular arrangements of the isotope being "excited". This signature is used to diagnose certain metabolic disorders, especially those affecting the brain,[61] and to provide information on tumor metabolism.[62]

Magnetic resonance spectroscopic imaging (MRSI) combines both spectroscopic and imaging methods to produce spatially localized spectra from within the sample or patient. The spatial resolution is much lower (limited by the available SNR), but the spectra in each voxel contains information about many metabolites. Because the available signal is used to encode spatial and spectral information, MRSI requires high SNR achievable only at higher field strengths (3 T and above).[citation needed]

Real-time MRI

Real-time MRI of a human heart at a resolution of 50 ms

Real-time MRI refers to the continuous monitoring ("filming") of moving objects in real time. While many different strategies have been developed since the early 2000s, a recent development reported a real-time MRI technique based on radial FLASH and iterative reconstruction that yields a temporal resolution of 20 to 30 milliseconds for images with an in-plane resolution of 1.5 to 2.0 mm. The new method promises to add important information about diseases of the joints and the heart. In many cases MRI examinations may become easier and more comfortable for patients.[63]

Interventional MRI

The lack of harmful effects on the patient and the operator make MRI well-suited for interventional radiology, where the images produced by an MRI scanner guide minimally invasive procedures. Such procedures must be done with no ferromagnetic instruments.[citation needed]

A specialized growing subset of interventional MRI is intraoperative MRI, in which doctors use an MRI in surgery. Some specialized MRI systems allow imaging concurrent with the surgical procedure. More typical, however, is that the surgical procedure is temporarily interrupted so that MRI can verify the success of the procedure or guide subsequent surgical work.[citation needed]

Magnetic resonance guided focused ultrasound

In MRgFUS therapy, ultrasound beams are focused on a tissue—guided and controlled using MR thermal imaging—and due to the significant energy deposition at the focus, temperature within the tissue rises to more than 65 °C (150 °F), completely destroying it. This technology can achieve precise ablation of diseased tissue. MR imaging provides a three-dimensional view of the target tissue, allowing for precise focusing of ultrasound energy. The MR imaging provides quantitative, real-time, thermal images of the treated area. This allows the physician to ensure that the temperature generated during each cycle of ultrasound energy is sufficient to cause thermal ablation within the desired tissue and if not, to adapt the parameters to ensure effective treatment.[64]

Multinuclear imaging

Hydrogen is the most frequently imaged nucleus in MRI because it is present in biological tissues in great abundance, and because its high gyromagnetic ratio gives a strong signal. However, any nucleus with a net nuclear spin could potentially be imaged with MRI. Such nuclei include helium-3, lithium-7, carbon-13, fluorine-19, oxygen-17, sodium-23, phosphorus-31 and xenon-129. 23Na and 31P are naturally abundant in the body, so can be imaged directly. Gaseous isotopes such as 3He or 129Xe must be hyperpolarized and then inhaled as their nuclear density is too low to yield a useful signal under normal conditions. 17O and 19F can be administered in sufficient quantities in liquid form (e.g. 17O-water) that hyperpolarization is not a necessity.[citation needed] Using helium or xenon has the advantage of reduced background noise, and therefore increased contrast for the image itself, because these elements are not normally present in biological tissues.[65]

Moreover, the nucleus of any atom that has a net nuclear spin and that is bonded to a hydrogen atom could potentially be imaged via heteronuclear magnetization transfer MRI that would image the high-gyromagnetic-ratio hydrogen nucleus instead of the low-gyromagnetic-ratio nucleus that is bonded to the hydrogen atom.[66] In principle, hetereonuclear magnetization transfer MRI could be used to detect the presence or absence of specific chemical bonds.[67][68]

Multinuclear imaging is primarily a research technique at present. However, potential applications include functional imaging and imaging of organs poorly seen on 1H MRI (e.g., lungs and bones) or as alternative contrast agents. Inhaled hyperpolarized 3He can be used to image the distribution of air spaces within the lungs. Injectable solutions containing 13C or stabilized bubbles of hyperpolarized 129Xe have been studied as contrast agents for angiography and perfusion imaging. 31P can potentially provide information on bone density and structure, as well as functional imaging of the brain. Multinuclear imaging holds the potential to chart the distribution of lithium in the human brain, this element finding use as an important drug for those with conditions such as bipolar disorder.[citation needed]

Molecular imaging by MRI

MRI has the advantages of having very high spatial resolution and is very adept at morphological imaging and functional imaging. MRI does have several disadvantages though. First, MRI has a sensitivity of around 10−3 mol/L to 10−5 mol/L, which, compared to other types of imaging, can be very limiting. This problem stems from the fact that the population difference between the nuclear spin states is very small at room temperature. For example, at 1.5 teslas, a typical field strength for clinical MRI, the difference between high and low energy states is approximately 9 molecules per 2 million. Improvements to increase MR sensitivity include increasing magnetic field strength, and hyperpolarization via optical pumping or dynamic nuclear polarization. There are also a variety of signal amplification schemes based on chemical exchange that increase sensitivity.[citation needed]

To achieve molecular imaging of disease biomarkers using MRI, targeted MRI contrast agents with high specificity and high relaxivity (sensitivity) are required. To date, many studies have been devoted to developing targeted-MRI contrast agents to achieve molecular imaging by MRI. Commonly, peptides, antibodies, or small ligands, and small protein domains, such as HER-2 affibodies, have been applied to achieve targeting. To enhance the sensitivity of the contrast agents, these targeting moieties are usually linked to high payload MRI contrast agents or MRI contrast agents with high relaxivities.[69] A new class of gene targeting MR contrast agents (CA) has been introduced to show gene action of unique mRNA and gene transcription factor proteins.[70][71] This new CA can trace cells with unique mRNA, microRNA and virus; tissue response to inflammation in living brains.[72] The MR reports change in gene expression with positive correlation to TaqMan analysis, optical and electron microscopy.[73]


In the UK, the price of a clinical 1.5-tesla MRI scanner is around £920,000/US$1.4 million, with the lifetime maintenance cost broadly similar to the purchase cost.[74] In the Netherlands, the average MRI scanner costs around €1 million,[75] with a 7-T MRI having been taken in use by the UMC Utrecht in December 2007, costing €7 million.[76] Construction of MRI suites could cost up to US$500,000/€370.000 or more, depending on project scope. Pre-polarizing MRI (PMRI) systems using resistive electromagnets have shown promise as a low-cost alternative and have specific advantages for joint imaging near metal implants, however they are likely unsuitable for routine whole-body or neuroimaging applications.[77][78]

A 3 tesla clinical MRI scanner.

MRI scanners have become significant sources of revenue for healthcare providers in the US. This is because of favorable reimbursement rates from insurers and federal government programs. Insurance reimbursement is provided in two components, an equipment charge for the actual performance and operation of the MRI scan and a professional charge for the radiologist's review of the images and/or data. In the US Northeast, an equipment charge might be $3,500/€2,600 and a professional charge might be $350/€260,[79] although the actual fees received by the equipment owner and interpreting physician are often significantly less and depend on the rates negotiated with insurance companies or determined by the Medicare fee schedule. For example, an orthopedic surgery group in Illinois billed a charge of $1,116/€825 for a knee MRI in 2007, but the Medicare reimbursement in 2007 was only $470.91/€350.[80] Many insurance companies require advance approval of an MRI procedure as a condition for coverage.

In the US, the Deficit Reduction Act of 2005 significantly reduced reimbursement rates paid by federal insurance programs for the equipment component of many scans, shifting the economic landscape. Many private insurers have followed suit.[citation needed]

In the United States, an MRI of the brain with and without contrast billed to Medicare Part B entails, on average, a technical payment of US$403/€300 and a separate payment to the radiologist of US$93/€70.[81] In France, the cost of an MRI exam is approximately €150/US$205. This covers three basic scans including one with an intravenous contrast agent as well as a consultation with the technician and a written report to the patient's physician.[82] In Japan, the cost of an MRI examination (excluding the cost of contrast material and films) ranges from US$155/€115 to US$180/€133, with an additional radiologist professional fee of US$17/€12.50.[83] In India, the cost of an MRI examination including the fee for the radiologist's opinion comes to around Rs 3000–4000 (€37–49/US$50–60), excluding the cost of contrast material. In the UK the retail price for an MRI scan privately ranges between £350 and £700 (€405–810).[84]


MRI is in general a safe technique, although injuries may occur as a result of failed safety procedures or human error.[85] Contraindications to MRI include most cochlear implants and cardiac pacemakers, shrapnel, and metallic foreign bodies in the eyes. The safety of MRI during the first trimester of pregnancy is uncertain, but it may be preferable to other options.[86] Since MRI does not use any ionizing radiation, its use is generally favored in preference to CT when either modality could yield the same information.[87] In certain cases, MRI is not preferred as it may be more expensive, time-consuming, and claustrophobia-exacerbating.

MRI uses powerful magnets and can therefore cause magnetic materials to move at great speeds posing risk. Deaths have occurred.[88]


Medical societies issue guidelines for when physicians should use MRI on patients and recommend against overuse. MRI can detect health problems or confirm a diagnosis, but medical societies often recommend that MRI not be the first procedure for creating a plan to diagnose or manage a patient's complaint. A common case is to use MRI to seek a cause of low back pain; the American College of Physicians, for example, recommends against this procedure as unlikely to result in a positive outcome for the patient.[89][90]


Motion artifact (T1 coronal study of cervical vertebrae).[91]

An MRI artifact is a visual artifact, that is, an anomaly during visual representation. Many different artifacts can occur during magnetic resonance imaging (MRI), some affecting the diagnostic quality, while others may be confused with pathology. Artifacts can be classified as patient-related, signal processing-dependent and hardware (machine)-related.[91] Artifacts remain a problematic in magnetic resonance imaging (MRI). Some affect the quality of the examination, while others may be confused with pathology.[91]

Non-medical use

MRI is used industrially mainly for routine analysis of chemicals. The nuclear magnetic resonance technique is also used, for example, to measure the ratio between water and fat in foods, monitoring of flow of corrosive fluids in pipes, or to study molecular structures such as catalysts.[92]


In the late 1970s, physicists Peter Mansfield and Paul Lauterbur, developed MRI-related techniques, like the echo-planar imaging (EPI) technique.[93] Mansfield and Lauterbur were awarded the 2003 Nobel Prize in Physiology or Medicine for their "discoveries concerning magnetic resonance imaging".

See also


  1. ^ Donald W. McRobbie, Elizabeth A. Moore, Martin J. Graves, Martin R. Prince, MRI from Picture to Proton, Cambridge University Press, 2007, ISBN 1139457195page 1
  2. ^ Smith-Bindman R; Miglioretti DL; Johnson E; Lee C; Feigelson HS; Flynn M; Greenlee RT; Kruger RL; Hornbrook MC; et al. (2012). "Use of diagnostic imaging studies and associated radiation exposure for patients enrolled in large integrated health care systems, 1996–2010". JAMA. 307 (22): 2400–9. doi:10.1001/jama.2012.5960. PMC 3859870Freely accessible. PMID 22692172. 
  3. ^ "Health at a glance 2009 OECD indicators". Health at a Glance. Health at a Glance. OECD. 2009. doi:10.1787/health_glance-2009-en. ISBN 9789264061538. ISSN 1995-3992. 
  4. ^ a b McRobbie, Donald W. (2007). MRI from picture to proton. Cambridge, UK; New York: Cambridge University Press. ISBN 0-521-68384-X. 
  5. ^ Sasaki M; Ehara S; Nakasato T; Tamakawa Y; Kuboya Y; Sugisawa M; Sato T (April 1990). "MR of the shoulder with a 0.2-T permanent-magnet unit". AJR Am J Roentgenol. 154 (4): 777–8. doi:10.2214/ajr.154.4.2107675. PMID 2107675. 
  6. ^ McDermott, Robert; et al. "Microtesla MRI with a superconducting quantum interference device" (PDF). Proceedings of the National Academy of Sciences. 101: 7857–7861. Bibcode:2004PNAS..101.7857M. doi:10.1073/pnas.0402382101. 
  7. ^ Zotev, Vadim; et al. "SQUID-based instrumentation for ultra-low-field MRI" (PDF). 
  8. ^ Vesanen, Panu; et al. "Hybrid ultra-low-field MRI and magnetoencephalography system based on a commercial whole-head neuromagnetometer". Magnetic Resonance in Medicine. 69: 1795–1804. doi:10.1002/mrm.24413. 
  9. ^ a b c d e f g h i j k l "Magnetic Resonance Imaging". University of Wisconsin. Retrieved 2016-03-14. 
  10. ^ a b c d e f g h i j k l m n o p q r Keith A. Johnson. "Basic proton MR imaging. Tissue Signal Characteristics". Harvard Medical School. Archived from the original on 2016-03-05. Retrieved 2016-03-14. 
  11. ^ a b Tushar Patil. "MRI sequences". Retrieved 2016-03-14. 
  12. ^ "Magnetic Resonance, a critical peer-reviewed introduction". European Magnetic Resonance Forum. Retrieved 17 November 2014. 
  13. ^ Hollingworth W; Todd CJ; Bell MI; Arafat Q; Girling S; Karia KR; Dixon AK (2000). "The diagnostic and therapeutic impact of MRI: an observational multi-centre study". Clin Radiol. 55 (11): 825–31. doi:10.1053/crad.2000.0546. PMID 11069736. 
  14. ^ Husband, J (2008). Recommendations for Cross-Sectional Imaging in Cancer Management: Computed Tomography – CT Magnetic Resonance Imaging – MRI Positron Emission Tomography – PET-CT (PDF). Royal College of Radiologists. ISBN 1 905034 13 X. 
  15. ^ American Society of Neuroradiology (2013). "ACR-ASNR Practice Guideline for the Performance and Interpretation of Magnetic Resonance Imaging (MRI) of the Brain" (PDF). 
  16. ^ Nolen-Hoeksema, Susan (2014). Abnormal Psychology (Sixth ed.). New York: McGraw-Hill Education. p. 67. 
  17. ^ Brown RA, Nelson JA (2016). "The invention and early history of the N-localizer for stereotactic neurosurgery". Cureus. 8 (6): e642. doi:10.7759/cureus.642. PMC 4959822Freely accessible. PMID 27462476. 
  18. ^ Leksell L; Leksell D; Schwebel J (1985). "Stereotaxis and nuclear magnetic resonance". Journal of Neurology, Neurosurgery & Psychiatry. 48 (1): 14–18. doi:10.1136/jnnp.48.1.14. PMC 1028176Freely accessible. PMID 3882889. 
  19. ^ Heilbrun MP; Sunderland PM; McDonald PR; Wells TH Jr.; Cosman E; Ganz E (1987). "Brown-Roberts-Wells stereotactic frame modifications to accomplish magnetic resonance imaging guidance in three planes". Applied Neurophysiology. 50 (1–6): 143–152. doi:10.1159/000100700. PMID 3329837. 
  20. ^ "ACCF/ACR/SCCT/SCMR/ASNC/NASCI/SCAI/SIR 2006 Appropriateness Criteria for Cardiac Computed Tomography and Cardiac Magnetic Resonance Imaging". Journal of the American College of Radiology. 3 (10): 751–771. 2006. doi:10.1016/j.jacr.2006.08.008. ISSN 1546-1440. 
  21. ^ Helms, C (2008). Musculoskeletal MRI. Saunders. ISBN 1416055347. 
  22. ^ Frydrychowicz A; Lubner MG; Brown JJ; Merkle EM; Nagle SK; Rofsky NM; Reeder SB (2012). "Hepatobiliary MR imaging with gadolinium-based contrast agents". J Magn Reson Imaging. 35 (3): 492–511. doi:10.1002/jmri.22833. PMC 3281562Freely accessible. PMID 22334493. 
  23. ^ Sandrasegaran K; Lin C; Akisik FM; Tann M (2010). "State-of-the-art pancreatic MRI". AJR Am J Roentgenol. 195 (1): 42–53. doi:10.2214/ajr.195.3_supplement.0s42. PMID 20566796. 
  24. ^ Masselli G; Gualdi G (2012). "MR imaging of the small bowel". Radiology. 264 (2): 333–48. doi:10.1148/radiol.12111658. PMID 22821694. 
  25. ^ Zijta FM; Bipat S; Stoker J (2010). "Magnetic resonance (MR) colonography in the detection of colorectal lesions: a systematic review of prospective studies". Eur Radiol. 20 (5): 1031–46. doi:10.1007/s00330-009-1663-4. PMC 2850516Freely accessible. PMID 19936754. 
  26. ^ Haacke, E Mark; Brown, Robert F; Thompson, Michael; Venkatesan, Ramesh (1999). Magnetic resonance imaging: Physical principles and sequence design. New York: J. Wiley & Sons. ISBN 0-471-35128-8. [page needed]
  27. ^ "MR Contrast Agents". 2014. 
  28. ^ Murphy KJ; Brunberg JA; Cohan RH (October 1996). "Adverse reactions to gadolinium contrast media: a review of 36 cases". AJR Am J Roentgenol. 167 (4): 847–9. doi:10.2214/ajr.167.4.8819369. PMID 8819369. 
  29. ^ "ACR guideline". guideline.gov. 2005. 
  30. ^ Thomsen HS; Morcos SK; Dawson P (November 2006). "Is there a causal relation between the administration of gadolinium based contrast media and the development of nephrogenic systemic fibrosis (NSF)?". Clin Radiol. 61 (11): 905–6. doi:10.1016/j.crad.2006.09.003. PMID 17018301. 
  31. ^ "FDA Drug Safety Communication: New warnings for using gadolinium-based contrast agents in patients with kidney dysfunction". Information on Gadolinium-Based Contrast Agents. U.S. Food and Drug Administration. 23 December 2010. Retrieved 12 March 2011. 
  32. ^ "FDA Public Health Advisory: Gadolinium-containing Contrast Agents for Magnetic Resonance Imaging". fda.gov. Archived from the original on 2006-09-28. 
  33. ^ [1] Archived January 17, 2013, at the Wayback Machine.
  34. ^ "ismrm.org MRI Questions and Answers" (PDF). Retrieved 2010-08-02. 
  35. ^ "Response to the FDA's May 23, 2007, Nephrogenic Systemic Fibrosis Update1 — Radiology". Radiology.rsna.org. 2007-09-12. Retrieved 2010-08-02. 
  36. ^ Dr Jeremy Jones and Prof Frank Gaillard. "MRI sequences (overview)". Radiopaedia. Retrieved 2017-10-15. 
  37. ^ Page 292 in: Martin Vosper, Donald Graham, Paul Cloke (2011). Principles and Applications of Radiological Physics (6 ed.). Elsevier Health Sciences. ISBN 9780702046148. 
  38. ^ Jeremy Jones and Prof Frank Gaillard; et al. "MRI sequences (overview)". Radiopaedia. Retrieved 2017-01-13. 
  39. ^ Lefevre, Nicolas; Naouri, Jean Francois; Herman, Serge; Gerometta, Antoine; Klouche, Shahnaz; Bohu, Yoann (2016). "A Current Review of the Meniscus Imaging: Proposition of a Useful Tool for Its Radiologic Analysis". Radiology Research and Practice. 2016: 1–25. doi:10.1155/2016/8329296. ISSN 2090-1941. 
  40. ^ a b Dr Tim Luijkx and Dr Yuranga Weerakkody. "Steady-state free precession MRI". Radiopaedia. Retrieved 2017-10-13. 
  41. ^ Mohammad Taghi Niknejad. "Short tau inversion recovery". Radiopaedia. Retrieved 2017-10-13. 
  42. ^ Ferco Berger, Milko de Jonge, Robin Smithuis and Mario Maas. "Stress fractures". Radiopaedia. Retrieved 2017-10-13. 
  43. ^ "Fluid attenuation inversion recoveryg". radiopaedia.org. Retrieved 2015-12-03. 
  44. ^ a b Dr Bruno Di Muzio and Dr Ahmed Abd Rabou. "Double inversion recovery sequence". Radiopaedia. Retrieved 2017-10-13. 
  45. ^ Neuro and Dr Usman Bashir. "Diffusion weighted imaging". Radiopaedia. Retrieved 2017-10-13. 
  46. ^ Dr Yuranga Weerakkody and Prof Frank Gaillard; et al. "Ischaemic stroke". Radiopaedia. Retrieved 2017-10-15. 
  47. ^ Mark Hammer. "MRI Physics: Diffusion-Weighted Imaging". XRayPhysics. Retrieved 2017-10-15. 
  48. ^ An, H.; Ford, A. L.; Vo, K.; Powers, W. J.; Lee, J.-M.; Lin, W. (2011). "Signal Evolution and Infarction Risk for Apparent Diffusion Coefficient Lesions in Acute Ischemic Stroke Are Both Time- and Perfusion-Dependent". Stroke. 42 (5): 1276–1281. doi:10.1161/STROKEAHA.110.610501. ISSN 0039-2499. 
  49. ^ a b Derek Smith and Dr Usman Bashir. "Diffusion tensor imaging". Radiopaedia. Retrieved 2017-10-13. 
  50. ^ Chua, Terence C; Wen, Wei; Slavin, Melissa J; Sachdev, Perminder S (2008). "Diffusion tensor imaging in mild cognitive impairment and Alzheimerʼs disease: a review". Current Opinion in Neurology. 21 (1): 83–92. doi:10.1097/WCO.0b013e3282f4594b. ISSN 1350-7540. 
  51. ^ Frank Gaillard; et al. "Dynamic susceptibility contrast (DSC) MR perfusion". Radiopaedia. Retrieved 2017-10-14. 
  52. ^ Chen, Feng (2012). "Magnetic resonance diffusion-perfusion mismatch in acute ischemic stroke: An update". World Journal of Radiology. 4 (3): 63. doi:10.4329/wjr.v4.i3.63. ISSN 1949-8470. 
  53. ^ Prof Frank Gaillard; et al. "Dynamic contrast enhanced (DCE) MR perfusion". Radiopaedia. Retrieved 2017-10-15. 
  54. ^ "Arterial spin labeling". University of Michigan. Retrieved 2017-10-27. 
  55. ^ Prof Frank Gaillard; et al. "Arterial spin labelling (ASL) MR perfusion". Radiopaedia. Retrieved 2017-10-15. 
  56. ^ Chou, I-han. "Milestone 19: (1990) Functional MRI". Nature. Retrieved 9 August 2013. 
  57. ^ Dr Tim Luijkx and Prof Frank Gaillard. "Functional MRI". Radiopaedia. Retrieved 2017-10-16. 
  58. ^ a b "Magnetic Resonance Angiography (MRA)". Johns Hopkins Hospital. Retrieved 2017-10-15. 
  59. ^ Dr J. Ray Ballinger; et al. "Phase contrast imaging". Radiopaedia. Retrieved 2017-10-15. 
  60. ^ Dr Bruno Di Muzio and A.Prof Frank Gaillard. "Susceptibility weighted imaging". Retrieved 2017-10-15. 
  61. ^ Rosen Y; Lenkinski RE (July 2007). "Recent advances in magnetic resonance neurospectroscopy". Neurotherapeutics. 4 (3): 330–45. doi:10.1016/j.nurt.2007.04.009. PMID 17599700. 
  62. ^ Golder W (June 2004). "Magnetic resonance spectroscopy in clinical oncology". Onkologie. 27 (3): 304–9. doi:10.1159/000077983. PMID 15249722. 
  63. ^ Uyanik, Ilyas; Lindner, Peggy; Tsiamyrtzis, Panagiotis; Shah, Dipan; Tsekos, Nikolaos V.; Pavlidis, Ioannis T. (2013). "Applying a Level Set Method for Resolving Physiologic Motions in Free-Breathing and Non-gated Cardiac MRI". 7945: 466–473. doi:10.1007/978-3-642-38899-6_55. ISSN 0302-9743. 
  64. ^ Cline HE; Schenck JF; Hynynen K; Watkins RD; Souza SP; Jolesz FA (1992). "MR-guided focused ultrasound surgery". J Comput Assist Tomogr. 16 (6): 956–65. doi:10.1097/00004728-199211000-00024. PMID 1430448. 
  65. ^ "Hyperpolarized Noble Gas MRI Laboratory: Hyperpolarized Xenon MR Imaging of the Brain". Harvard Medical School. Retrieved 2017-07-26. 
  66. ^ Hurd RE; John BK (February 1991). "Gradient-enhanced proton-detected heteronuclear multiple-quantum coherence spectroscopy". Journal of Magnetic Resonance, Series A. 91 (3): 648–653. Bibcode:1991JMagR..91..648H. doi:10.1016/0022-2364(91)90395-a. 
  67. ^ Brown RA; Venters RA; Tang PPPZ; Spicer LD (March 1995). "A test for scalar coupling between heteronuclei using gradient-enhanced proton-detected HMQC spectroscopy". Journal of Magnetic Resonance, Series A. 113 (1): 117–119. Bibcode:1995JMagR.113..117B. doi:10.1006/jmra.1995.1064. 
  68. ^ Miller AF; Egan LA; Townsend CA (March 1997). "Measurement of the degree of isotopic enrichment of different positions in an antibiotic peptide by NMR" (PDF). Journal of Magnetic Resonance. 125 (1): 120–131. Bibcode:1997JMagR.125..120M. doi:10.1006/jmre.1997.1107. PMID 9245367. 
  69. ^ Xue S; Qiao J; Pu F; Cameron M; Yang JJ (2013). "Design of a novel class of protein-based magnetic resonance imaging contrast agents for the molecular imaging of cancer biomarkers". Wiley Interdiscip Rev Nanomed Nanobiotechnol. 5 (2): 163–79. doi:10.1002/wnan.1205. PMC 4011496Freely accessible. PMID 23335551. 
  70. ^ Liu CH; Kim YR; Ren JQ; Eichler F; Rosen BR; Liu PK (2007). "Imaging cerebral gene transcripts in live animals". J. Neurosci. 27 (3): 713–22. doi:10.1523/JNEUROSCI.4660-06.2007. PMC 2647966Freely accessible. PMID 17234603. 
  71. ^ Liu CH; Ren J; Liu CM; Liu PK (2014). "Intracellular gene transcription factor protein-guided MRI by DNA aptamers in vivo". FASEB J. 28 (1): 464–73. doi:10.1096/fj.13-234229. PMID 24115049. 
  72. ^ Liu CH; You Z; Liu CM; Kim YR; Whalen MJ; Rosen BR; Liu PK (2009). "Diffusion-weighted magnetic resonance imaging reversal by gene knockdown of matrix metalloproteinase-9 activities in live animal brains". J. Neurosci. 29 (11): 3508–17. doi:10.1523/JNEUROSCI.5332-08.2009. PMC 2726707Freely accessible. PMID 19295156. 
  73. ^ Liu CH; Yang J; Ren JQ; Liu CM; You Z; Liu PK (2013). "MRI reveals differential effects of amphetamine exposure on neuroglia in vivo". FASEB J. 27 (2): 712–24. doi:10.1096/fj.12-220061. PMC 3545538Freely accessible. PMID 23150521. 
  74. ^ "Managing high value capital equipment in the NHS in England" (PDF). National Audit Office (United Kingdom). Archived from the original (PDF) on 3 December 2013. Retrieved 30 November 2013. 
  75. ^ "MRI-scanner big financial success for Philips (Dutch)". Eindhovens Dagblad (ED). Retrieved 18 February 2009. 
  76. ^ "MRI scanner of €7 million in use(Dutch)". Medisch Contact. Archived from the original on 4 September 2015. Retrieved 5 December 2007. 
  77. ^ Morgan P; Conolly S; Scott G; Macovski A (1996). "A readout magnet for prepolarized MRI". Magn Reson Med. 36 (4): 527–36. doi:10.1002/mrm.1910360405. PMID 8892203. 
  78. ^ Blamire AM (2008). "The technology of MRI--the next 10 years?". Br J Radiol. 81 (968): 601–17. doi:10.1259/bjr/96872829. PMID 18628329. 
  79. ^ Stamford Hospital price quotation October 2008, Stamford CT US
  80. ^ Goldstein, Wayne M.; Gordon, Alexander C.; Branson, Jill Jasperson; Simmons, Christopher; Berland, Kimberly; Willsey, Daniel S.; Andrews, Amanda L. (March 5–9, 2008). Over-Utilization of MRI in the Osteoarthritis Patient (PDF). Annual Meeting AAOS. San Francisco. 
  81. ^ Current Procedural Terminology code #70553 "2010 Medicare Part B National Summary Data File". Data.gov, An Official Website of the United States Government.
  82. ^ "How long does an MRI take?". Htdiary.com. HealthDiary. 
  83. ^ Ehara S; Nakajima Y; Matsui O (August 2008). "Radiology in Japan in 2008". AJR Am J Roentgenol. 191 (2): 328–9. doi:10.2214/AJR.07.3940. PMID 18647897. 
  84. ^ "Private MRI Scan". Fairfield.org.uk. Fairfield Independent Hospital. Retrieved 2017-03-28. 
  85. ^ Watson, Robert E. (2015-10-01). "Lessons Learned from MRI Safety Events". Current Radiology Reports. 3 (10): 37. doi:10.1007/s40134-015-0122-z. ISSN 2167-4825. 
  86. ^ Wang PI; Chong ST; Kielar AZ; Kelly AM; Knoepp UD; Mazza MB; Goodsitt MM (2012). "Imaging of pregnant and lactating patients: part 1, evidence-based review and recommendations". AJR Am J Roentgenol. 198 (4): 778–84. doi:10.2214/AJR.11.7405. PMID 22451541. 
  87. ^ "iRefer". Royal College of Radiologists. Retrieved 10 November 2013. 
  88. ^ Man dies after being sucked into MRI scanner at Indian hospital The Guardian, 2018
  89. ^ Consumer Reports; American College of Physicians. presented by ABIM Foundation. "Five Things Physicians and Patients Should Question" (PDF). Choosing Wisely. Consumer Reports. Archived from the original (PDF) on June 24, 2012. Retrieved August 14, 2012. 
  90. ^ Consumer Reports; American College of Physicians (April 2012). presented by Annals of Internal Medicine. "Imaging tests for lower-back pain: Why you probably don't need them" (PDF). High Value Care. Consumer Reports. Retrieved August 14, 2012. 
  91. ^ a b c Erasmus, L.J.; Hurter, D.; Naude, M.; Kritzinger, H.G.; Acho, S. (2004). "A short overview of MRI artifacts". South African Journal of Radiology. 8 (2). doi:10.4102/sajr.v8i2.127. ISSN 2078-6778.  (CC-BY 4.0)
  92. ^ "Chapter Nineteen Non-Medical Applications of NMR and MRI". Magnetic Resonance (11 ed.). 2017. Retrieved 2017-12-18. 
  93. ^ Mansfield P; Grannell, P (1975). "Diffraction and microscopy in solids and liquids by NMR". Physical Review B. 12 (9): 3618–3634. Bibcode:1975PhRvB..12.3618M. doi:10.1103/physrevb.12.3618. 

Further reading

External links