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774 Current Concepts of Cerebrovascular Disease and Stroke Magnetic Resonance Angiography Cerebrovascular Applications Paul M. Ruggieri, MD; Thomas J. Masaryk, MD; and Jeffrey S. Ross, MD M Downloaded from http://stroke.ahajournals.org/ by guest on May 6, 2017 agnetic resonance angiography (MRA) can provide significant additional information to complement the routine spin-echo MR examination of the brain.1"13 The idea of a combined study has gained favor because it provides a noninvasive alternative for the complete study of patients with suspected cerebrovascular disease. Because of the relatively short time of acquisition, MRA sequences can be easify added to the traditional parenchymal study without significantly prolonging the overall examination time (Figure 1). Magnetic resonance is able to create anatomic images through the use of radiofrequency (RF) excitation and refocusing pulses as well as spatial localizing magnetic field gradients. Motion (blood flow) in the presence of the RF pulse sequence creates time-of-flight (TOF) effects on the signal of moving protons, while proton motion during the application and in the direction of the magnetic field gradients produces spin phase phenomena. Each of these effects can be manipulated relatively independently to create vascular contrast within a given scan and thus angiographic images. TOF techniques create vascular contrast via the inflow of blood protons into a region of interest previously prepared by an RF excitation, inversion, or saturation pulse. The most popular techniques consist of relatively simple gradient echo pulse sequences where the inflow of spins produces high signal within the vessels on the basis of the TOF effects known as "entry slice phenomenon" or "flow-related enhancement." Angiographic images can then be derived from such data sets through the use of computer post-processing techniques which obviate the need for mask acquisitions to create a subtraction angiogram. Since TOF MRA requires only a single data set, the acquisition is less susceptible to problems, such as patient motion and eddy currents, which arise with longer examination times and multiple data sets.111 TOF data also require less computer memory and post-processing following the acquisition. Although the phase contrast techniques are more sensitive to very slow flow, the TOF techniques may be less vulnerable to the phase dispersion (and signal loss) that accompanies complex motion typically seen in regions of arterial flow (i.e., tortuous vessels, stenoses).12-13 All MRA techniques may be implemented in a 2D or 3D mode. Two-dimensional Fourier transform imaging (2DFT) acquires data in the conventional fashion in which individually acquired image slices are stacked sequentially. With 3D Fourier transform (3DFT) acquisitions an entire block or "slab" of anatomic digital data is acquired. This may then be displayed as individual slices reconstructed in any plane or perhaps subjected to a post-processing algorithm which displays only selected tissues (Figure 1). While 2D MRA examinations are superior for the demonstration of slow flow (e.g., venous) lesions, 3DFT sequences can provide thinner image slices with higher spatial resolution, as well as shorter echo times which minimize artifact responsible for the overestimation of (carotid) stenoses. TOF techniques have been most extensively tested in the evaluation of carotid artery atherosclerotic disease and a variety of vascular abnormalities involving the larger vessels of the intracranial circulation. Both areas are particularly amenable to investigation by TOF studies because of the relatively rapid, constant flow in these vessels (particularly the carotid arteries) which results in high vascular contrast, the lack of significant physiologic motion (e.g., respiration), and the availability of coils which are especially well suited to these applications. With the exception of venous studies, intracranial investigations have been primarily performed with 3D sequences because of the complex flow and the demands for high spatial resolution.16-10 The carotid arteries have been studied with both 2D and 3D sequences.2-4 Extracranial Applications: Carotid Bifurcation MRA techniques will likely have their greatest clinical impact in the evaluation of carotid bifurcation atherosclerotic disease.14-15 Traditional MR imaging is particularly sensitive to the parenchymal sequelae of cerebral vascular disease, and many patients are now evaluated by MR for the extent and distribution of ischemic damage. Hence the interest in developing a technique that can be combined with the traditional MR brain examination to evaluate the severity of carotid bifurcation occlusive disease in the same sitting.14 A number of studies have been conducted which demonstrate the efficacy of 2D and 3D-TOF MRA techniques in the evaluation of the carotid bifurcation.2-41617 The sequential 2D-MRA technique has the advantage of high vessel/soft tissue contrast from strong flow-related enhancement which is maintained even in the setting of relatively slow flow (e.g., severe, long segment stenosis). On the other hand, minor motion by From the Section of Neuroradiology, Cleveland Clinic Foundathe patient during the scan can cause a severe stair-step tion, Cleveland, Ohio. Reprinted from Current Concepts of Cerebrovascular Disease and misregistration artifact. Also, higher gradient strengths are necessary to define thin slices in sequential 2DFT Stroke 1991;26:29-36. Ruggieri et al Cerebrovascular Applications of MRA 775 Initial studies have shown a high degree of correlation in the degree of stenosis when comparing 3D-TOF MRA images (using a single thick volume) with the accepted gold standard, intra-arterial digital subtraction angiography (IADSA).2-19 Estimation of the vessel caliber was not significantly impaired by local field inhomogeneities or the complex motion within and immediately distal to the stenoses.19 The more severe stenoses (greater than or equal to 70%) tended to be slightly overestimated as a result of these higher order motion terms, but this degree of error was felt to be acceptable for the purpose of a screening examination. Other clinical studies have suggested that an accurate evaluation of carotid occlusive disease may be possible noninvasively through a combination of 2D or 3D-TOF MRA and ultrasound examinations of the carotid arteries.20-21 Downloaded from http://stroke.ahajournals.org/ by guest on May 6, 2017 FIGURE 1. Normal MR angiographic study of the intracranial circulation. Anteroposterior (A) and left anterior oblique (B) maximum intensity projections of an axial volume sequence, obtained with 64 slices and a rectangular field of view, allow for high spatial resolution with an overall imaging time of 5 min, 50 sec. There is good definition of the carotid siphons bilaterally (open arrows), the basilar artery (short arrow), and the more distal branches such as the anterior (long arrow) and middle cerebral arteries (curved arrows) and the posterior cerebral arteries. Spatial resolution is sufficient to allow visualization of the superior cerebellar artery (two small arrows). imaging. This requirement places limitations on the spatial resolution and the echo time which can be implemented in these sequences. Both factors contribute to the degree of phase dispersion within the individual voxels. As a result the signal from the protons is partially (or completely) cancelled, and the carotid artery may be incompletely visualized in regions of severe narrowing. Lower gradients are needed to define the larger 3D volumes. After excitation of a large 3D volume or "slab," individual slices are spatially defined by phase encoding in the slice-select direction. The resultant thinner individual slices, higher in-plane spatial resolution, and shorter echo times in the 3D acquisitions reduce the variation of phase across each voxel.2 Consequently, less intravascular signal loss should occur in the region of local field inhomogeneities (e.g., air, calcification) or higher order motion terms (acceleration, jerk, turbulence) of the arterial blood at the site of narrowing. The reduced phase dispersion translates into improved vessel definition. The main disadvantage of the 3D studies is the potential saturation of slowly moving spins in areas far "down-stream" within the volume or distal to a severe stenosis (Figure 2). Thin, overlapping, stacked 3D volumes have been proposed as a solution to this problem although a 'Venetian blind" artifact can be introduced, which is related to signal variations at the edges of the volumes or patient movement between the different acquisitions.18 Motion artifact can also be a problem since it is reflected along two planes because of the additional phase-encoding gradient used in the slice-select direction in the 3D studies.2 Intracranial Applications TOF MRA has been applied in the head to the evaluation of patients with intracranial aneurysms, large vessel atherosclerotic disease, arteriovenous malformations, and dural sinus occlusions. Each of these entities has its own unique parenchymal sequelae which are investigated by the accompanying spin-echo examination. The MRA images enhance the specificity of the traditional brain study and provide additional information to the clinician and neuroradiologist to aid in making a decision regarding a subsequent invasive study or management. Aneurysms With an acute subarachnoid hemorrhage and a presumed intracranial aneurysm, patients are more appropriately studied by nonenhanced CT and conventional arteriography. The combination of an MRA and a conventional spin-echo study is better implemented in patients with a subacute onset of symptoms in whom an aneurysm might explain the clinical presentation (Figure 3). It is also appealing to consider using MRA as a screening test in patients with an increased risk of aneurysms (e.g., family history, polycystic kidney disease, fibromuscular disease, aortic coarctation). Preliminary retrospective studies comparing 3D-TOF MRA images with IADSA have yielded promising results.18-9 Ross et al8 detected aneurysms as small as 3-4 mm with sensitivities of 67% when evaluating the MRA images alone and 86% when evaluating the MRA images along with the original 3D slices and spin-echo images. Nevertheless, TOF images are still somewhat limited by the nature of the pathology, the technique itself, and hardware limitations. Hypointense thrombus in the aneurysm lumen (e.g., acute or chronic thrombosis) may artificially reduce or obliterate the aneurysm's lumen, but the same problem exists with catheter arteriography. Correlation with the spin-echo exam, the original 3D slices, or multiplanar reconstructions of these slices provides a more accurate assessment of the aneurysm lumen in this situation. Parenchymal and subarachnoid hemorrhage can also be misleading because the high intensity of subacute hemorrhage will also be picked up by the reconstruction program and may obscure the aneurysm. A large aneurysm or one that is compressing the lumen of the parent vessel may be poorly or 776 Stroke Vol 23, No 5 May 1992 FIGURE 2. Severe left carotid stenosis. (A) T2-weigfUed axial spin-echo study of the brain demonstrates a left hemispheric infarct. (B) An inferior slice through the level of the cavernous sinus shows absence of the normal flow void from the left carotid siphon (arrow) representing either thrombosis or very slow flow. Compare the left cavernous carotid with the normal flow void on the right (open arrow). (C) Lateral maximum intensity projection MR angiogram of the left carotid bifurcation demonstrates abrupt termination of the signal from the origin of the left internal carotid artery, suspicious for occlusion. Downloaded from http://stroke.ahajournals.org/ by guest on May 6, 2017 (D) However, a second axial intracranial MRA (submentovertex view) centered on the circle of Willis demonstrates flow within the left carotid siphon (arrow) and distal left internal carotid artery. The signal intensity within the left carotid siphon is less than that on the right (open arrow), presumably because of slow flow within the siphon with resultant saturation of the signal intensity. Slowed flow and saturation of signal distal to the severe stenosis also explain the apparent total occlusion of the proximal internal carotid artery (double arrowheads, middle cerebral arteries; single arrowheads, posterior cerebral arteries). Because of the residual signal intensity from the left carotid siphon, the examination was interpreted as a high-grade stenosis of the left internal carotid origin but not a complete occlusion. (E,F) Lateral views from the intra-arterial DSA study confirm the severe stenosis (arrow) involving the origin of the left internal carotid artery (E) with slowed flow in a patent cervical internal carotid artery (F) (arrows). incompletely visualized because of impaired inflow of the fresh, unsaturated spins which provides the flowrelated enhancement necessary to see the aneurysm lumen.9 Vasospasm may have the same effect. (Phase contrast techniques may not be subject to such prob- lems.12-13) Although less a problem with the 3D-TOF method, the parent vessel may be difficult to see if the spins moving within this segment demonstrate a large amount of higher order motion. Regardless, the 3D relation between the aneurysm and the parent vessel is Ruggieri et al Cerebrovascular Applications of MRA 777 Downloaded from http://stroke.ahajournals.org/ by guest on May 6, 2017 FIGURE 3. Left ophthalmic artery aneurysm. Anteroposterior (AP) (A) and lateral (B) maximum intensity projections from an axial volume MR angiographic sequence demonstrate a large, rounded area of increased signal intensity involving the superior aspect of the left carotid siphon (open arrow) in the region of the origin of the left ophthalmic artery (arrow). Basilar artery signal (arrowhead) overlaps the aneurysm on the AP view but is definitely posterior to the aneurysm on the lateral projection. Comparison AP (C) and lateral views (D) from the intra-arterial DSA study confirm the presence of a large aneurysm arising from the origin of the ophthalmic artery in a configuration and size similar to that defined by the MR angiographic study. still generally visible either on the MR arteriogram images or in multiplanar reconstructions of the high resolution 3D data sets. Arterial Occlusive Disease Preliminary clinical studies have also demonstrated the ability of 3D-TOF MRA to identify occlusive disease of the larger intracranial vessels.1-5'10-22 Confirmation of a tandem lesion in the distal internal carotid artery or an isolated stenosis in the proximal middle cerebral artery can have a significant impact on the clinical decision-making process in a patient with atherosclerotic narrowing at the carotid bifurcation. This may lead to a more definitive catheter study, for example, in a patient who has had a prior ultrasound examination documenting mild to moderate carotid bifurcation disease. On the other hand, a negative study may avoid a conventional angiogram. This option would be particularly valuable in older patients with suspected occlusive disease of the posterior circulation where the risk of the procedure itself is quite high. MRA may also permit noninvasive imaging of acute middle cerebral artery embolic occlusion, which is potentially treatable with thrombolytic agents. The studies conducted to date have demonstrated occlusion or stenosis of the distal internal carotid artery or the Ml segment of the middle cerebral artery. A group of infants with a ligated internal carotid artery and internal jugular vein (for extracorporeal membrane oxygenation) were studied to confirm adequate crossfilling and venous drainage for both cerebral hemi- spheres. These results provided significant long-term prognostic information about the children.5 Children with sickle cell disease were also studied to identify large vessel occlusive disease.10-22 The combination of MRA and a spin-echo parenchymal study can directly visualize the vascular stenosis and the parenchymal consequences in the corresponding vascular territory at the same sitting. Without additional acquisition time the corresponding phase images can be examined to document the direction of flow in other large vessels that may be supplying collateral flow. Selective MRA studies have also been designed to confirm the contributions from other vascular territories.23 An appropriately positioned saturation pulse, for example, can eliminate the inflow from one internal carotid artery to determine the extent of collateral flow (from the circle of Willis) to the territory of a severely stenotic carotid siphon. Little has been done to evaluate occlusive disease of the posterior circulation specifically. Since the vascular disorders of the posterior fossa, such as dissection and partial basilar artery thrombosis, tend to have relatively slow flow, an appropriately designed sequential 2D study would be the most successful TOF study. Although the vascular abnormality is frequently apparent on the spin-echo images, MRA can be helpful to confirm the pathology in those cases with confusing intraluminal signal. The TOF images themselves can be confusing with incomplete, subacute thrombosis of the basilar artery. Evaluation of the corresponding phase images can settle the issue. 778 Stroke Vol 23, No 5 May 1992 Difficulties similar to those which arise in the evaluation of stenosis of the carotid bifurcation are also demonstrated in the examination of intracranial occlusive disease. Because of higher order motion terms in the blood flowing within and immediately distal to the stenoses, the resulting phase dispersion causes an overestimation of the degree of stenosis. An additional complicating factor in the head is the size of even the larger intracranial vessels. Hardware limitations (i.e., system gradient capability) in the commercially available whole-body imaging systems impose restrictions on the echo time and spatial resolution which affect the degree to which these problems can be addressed. Downloaded from http://stroke.ahajournals.org/ by guest on May 6, 2017 Vascular Malformations TOF MRA images can provide useful information in the evaluation of parenchymal and dural arteriovenous (AV) fistulas. A venous angioma typically appears on conventional MR as a single large vessel extending from the ventricular margin to the cortical surface. The very slow flow and small size of the feeding vessels in cavernous angiomas and capillary telangiectasias prevent their visualization by any form of MRA. In any event the clinically significant cavernous angiomas are generally recognizable on the spin-echo examination by the blood products from prior hemorrhage. Parenchymal AV fistulas are visible because of the cluster of flow voids representing the nidus, the associated ischemic steal, or the results of prior intervention (e.g., surgery, embolization). Preliminary clinical results have shown that MRA is useful in demonstrating the 3D relations between the vascular nidus and the primary afferent and efferent vessels.16-13'24'25 Dural fistulas are unique in that they are frequently undetectable with routine MR imaging unless the excessive flow causes enlargement of the cortical veins or venous thrombosis.26 In these cases the preliminary clinical diagnosis is confirmed by the MRA images. The rapid, complex flow in the larger afferent arteries make the 3D-T0F MRA sequences desirable for imaging AV fistulas. Shorter echo times and the thinner 3D slices also effectively reduce the motion-induced dephasing which is necessary to visualize these arteries accurately. On the other hand, the saturation of the inflowing spins impairs the visualization of the slower flow in the smaller arteries and veins.1-6'11-18 High vessel/ soft tissue contrast is better maintained throughout the imaging volume with the use of a 2D-TOF technique. Although the smaller arteries and veins are better seen with this approach, the large afferent vessels are incompletely visualized because of the necessarily thicker slices and longer echo times.24 The best compromise seems to be the use of small, overlapping 3D volumes to combine the advantages of both the 2D and 3D techniques.6'18 If this 3D MRA is combined with intravenous gadolinium, the difficulty with spin saturation (and intravascular signal loss) in the draining veins and distal nidus vessels is further reduced.6 Regardless of the technique MRA cannot provide the physiologic information that can be derived from traditional catheter angiography such as the arteriovenous circulation time and arterial stump pressures. Edelman et al23-24 showed that it was possible to obtain some functional information with respect to identifying feed- ing vessels through the use of appropriately positioned saturation pulses. Saturation of one main feeding vessel prevents the inflow of fresh spins from that artery. A simple 2D-TOF image of the nidus, with the selective saturation pulse, would show a smaller or less intense nidus if that vessel contributed significantly to the malformation. Dural Sinus Occlusion The question of occlusion of the dural venous sinuses is often raised in patients with predisposing disease processes, such as adjacent paranasal sinus or parenchymal infection, head trauma, dehydration, or hypercoagulable states. Previously, the only definitive means of diagnosing such an occlusion was through invasive studies. With the advent of MR and MRA, an invasive study can be avoided. It is often possible to identify occlusion of the larger dural sinuses on the routine spin-echo images of the head. This is best evaluated on the late echo T2-weighted images, which are oriented perpendicular to the primary direction of flow for the sinus in question. With this arrangement the spins in the sinus are least apt to experience both the 90 and 180 pulses such that a flow void will be seen in the images if flow is present. For example, axial images would be most likely to demonstrate a flow void in the sigmoid sinus in a patient who was studied because of severe mastoiditis or a cholesteatoma which had caused bony destruction of the petrous ridge. Alternatively, coronal images would be the most appropriate orientation for patients with a parasagittal mass lesion compressing the adjacent superior sagittal sinus. On occasion the spin-echo images demonstrate confusing intraluminal signal in the sinuses, particularly if the T2-weighted study is not optimally oriented for the sinus in question (e.g., atypical anatomy), the slices are relatively thick, the second echo is relatively short, the venous flow is quite slow, or the sinus contains acute thrombus (isointense on Tl- and hypointense on T2weighted images). In such cases TOF MRA studies of the dural sinuses can provide more definitive information with little additional examination time.27 The slow flow in the dural sinuses demands the use of a 2D-TOF study. Visualization of the dural sinuses would be impaired by saturation effects in a 3D-TOF study unless the 3D study was performed after intravenous gadolinium administration.28 Potentially, 2D-TOF studies can provide misleading information if the sinus contains subacute thrombus and this is not apparent on the spin-echo study. The high signal intensity of the extracellular methemoglobin can mimic flow-related enhancement and suggest patency. Reconstructing the phase images from the spin-echo study can eliminate this ambiguity without prolonging scan time. Sequences can be designed such that the images are sensitive to flow in the slice-select direction as slow as 0.5 cm/sec or as slow as 2.5 cm/sec in the frequency direction.2930 It is also possible to quantitate the flow velocities in the sinuses through the use of paired gradient-recalled sequences or narrow in-plane saturation pulses (i.e., bolus tagging).31 Future Prospects Large, carefully controlled, prospective clinical trials must still be conducted to define more clearly the role Ruggieri et al Cerebrovascular Applications of MRA MRA will play in the evaluation of patients with clinically suspected cerebral vascular disease. At the moment TOF-MRA images cannot replace traditional arteriography of the carotid arteries and intracranial vasculature. The discrepancy between the modalities is particularly evident in the intracranial circulation where the spatial resolution demands are high. Irregularity of the vessel caliber is related, in part, to errors introduced by the maximum intensity projection post-processing algorithm used with present TOF angiography sequences. The most commonly used maximum intensity projection technique may be unable to identify accurately the vessels in the original data because of variations in the background signal intensity, inadequate flow-related enhancement, and/or volume averaging effects.32 These problems have stimulated the development of alternative, more sophisticated post-processing algorithms and the use of various background suppression techniques for the MRA acquisitions. Downloaded from http://stroke.ahajournals.org/ by guest on May 6, 2017 Another important factor contributing to the irregularity of a vessel lumen and focal discontinuities in a vessel is the intravascular phase dispersion secondary to complex motion and local field inhomogeneities. Reducing the minimum field echo time limits the motioninduced dephasing and was shown to be possible on routine imaging systems through the use of truncated RF pulses and asymmetric data sampling.7 Other innovations in data post-processing and image reconstruction should complement these strategies and improve the clinical usefulness of the MR arteriograms.33-35 Further reductions in the field echo time and voxel dimensions have been achieved through the use of specialized head coils with serf-contained gradients. These coils have higher peak gradient strengths and permit more rapid switching times than the standard imaging coils. Preliminary tests with prototype gradient RF head coils have shown the expected but nevertheless exciting results in phantoms and normal volunteers.36-37 Although these sequences have not yet been extensively tested in patients, it is expected that the MR arteriograms will display a significantly higher correlation with the traditional angiographic images than was demonstrated previously and the technique will therefore be of greater diagnostic value. References 1. Masaryk TJ, Modic MT, Ross JS, Ruggieri PM, Laub G, Lenz G, Haacke EM, Selman W, Wiznitzer M, Harik SI: Intracranial circulation: Preliminary clinical results with three-dimensional (volume) MR angiography. Radiology 1989;171:793-799 2. Masaryk TJ, Modic MT, Ruggieri PM, Ross JS, Laub G, Lenz GW, Tkach JA, Haacke EM, Selman WR, Harik SI: Three-dimensional (volume) gradient-echo imaging of the carotid bifurcation: Preliminary clinical experience. Radiology 1989;171:801-806 3. Edelman RR, Wentz KU, Mattle H, Zhao B, Liu C, Kim D, Laub G: Projection arteriography and venography: Initial clinical results with MR. Radiology 1989;172:351-357 4. Keller PJ, Drayer BP, Fram EK, Williams KD, Dumoulin CL, Souza SP: MR angiography with two-dimensional acquisition and three-dimensional display. Radiology 1989;173:527-532 5. Lewin JS, Masaryk TJ, Modic MT, Ross JS, Stork EK, Wiznitzer M: Extracorporeal membrane oxygenation in infants: Angiography and parenchymal evaluation of the brain with MR imaging. Radiology 1989;173:361-365 6. Marchal G, Bosnians H, Van fraeyenhoven L, Wilms G, Van Hecke P, Plets C, Baert AL: Intracranial vascular lesions: Optimization and clinical evaluation of three-dimensional time-of-flight MR angiography. Radiology 1990;175:443-448 779 7. Schmalbrock P, Yuan C, Chakeres DW, Kohli J, Pelc NJ: Volume MR angiography: Methods to achieve very short echo times. Radiology 1990;175:861-865 8. Ross JS, Masaryk TJ, Modic MT, Ruggieri PM, Haacke EM, Selman WR: Intracranial aneurysms: Evaluation by MR angiography. AJNR 1990;ll:449-456 9. Sevick RJ, Tsuruda JS, Schmalbrock P: Three-dimensional timeof-flight MR angiography in the evaluation of cerebral aneurysms. J Comput Assist Tomogr 1990;14:874-881 10. Wiznitzer M, Ruggieri PM, Masaryk TJ, Ross JS, Modic MT, Berman B: Diagnosis of cerebrovascular disease in sickle cell anemia by magnetic resonance angiography. / Pedialr 1990; 117: 551-555 11. Dumoulin CL, Cline HE, Souza SP, Wagle WA, Walker WF: Three-dimensional time-of-flight magnetic resonance angiography using spin saturation. Magn Reson Med 1989;lU5-46 12. Grist TM, Boyko OB, Spritzer CE, MacFall JR, Dumoulin CL, Souza SP, Keller PJ: Integration of MR imaging with MR angiography. Comparison of projection phase contrast techniques and flow related enhancement sequences for neurologic imaging. Presented at meeting of Radiological Society of North America, 1989 13. Pernicone JR, Siebert JE, Potchen EJ, Pera A, Dumoulin CL, Souza SP: Three-dimensional phase-contrast MR angiography in the head and neck: Preliminary report. AJNR 1990;ll:457-466 14. Kricheff II: Arteriosclerotic ischemic cerebrovascular disease. Radiology 1987;162:101-109 15. North American Symptomatic Carotid Endarterectomy Trial (NASCET): Benefit of carotid endarterectomy for patients with high-grade stenosis of the internal carotid artery. Clinical Alert News, National Library of Medicine, National Institutes of Health, March, 1991 16. Dixon WT, Du LN, Gado M, Rossnick S: Projection angiograms of blood labeled by adiabatic fast passage. Magn Reson Med 1986;3: 454-462 17. Nishimura DG, Macovski A, Pauly JM, Conolly SM: MR angiography by selective inversion recovery. Magn Reson Med 1987;4: 193-202 18. Blatter DD, Parker DI, Schwartz R, Robinson RO: Intracranial MR angiography with multiple thin-slab three-dimensional acquisition: Preliminary clinical experience in 80 patients (abstract). Radiology 1990;177(P):89 19. Masaryk TJ, Ross JS, Masaryk AM, Ruggieri PM, Selman W, Harik S: Quantitative comparison of MR angiography and digital subtraction angiography in the evaluation of carotid arterial disease. Presented at the 75th annual meeting, Radiological Society of North America, Chicago, Nov 26-Dec 1, 1989 20. Porges R, Grist TM, Boyko OB, Yuan C, Schmalbrock P, Kliewer M, Carroll B: Potential role of MR angiography as a screening modality for carotid artery disease (abstract). Radiology 1990; 177(P):89 21. Litt AW, Eidelman E, Pinto RS, Riles TS, McLachlan SJ, Schwartzenberg ST, Weinrab JC, Kricheff II: A blinded comparison of contrast arteriography, MR angiography, and Duplex US in the evaluation of the carotid bifurcation (abstract). Radiology 1990;177(P):90 22. Wiznitzer M, Masaryk TJ: Cerebrovascular abnormalities in pediatric stroke: Diagnosis using magnetic resonance angiography (abstract). Ann Neurol 1989;26:440-441 23. Edelman RR, Heinrich P, Mattle HP, O'Reilly GV, Wentz KU, Liu C, Zhao B: Magnetic resonance imaging of flow dynamics in the circle of Willis. Stroke 1990^1:56-65 24. Edelman RR, Wentz KU, Mattle HP, O'Reilly GV, Candia G, Liu C, Zhao B, Kjellberg RN, Davis KR: Intracerebral arteriovenous malformations: Evaluation with selective MR angiography and venography. Radiology 1989;173:831-837 25. Turski PA, Partington C, Koresec F, Mistretta C, Levine R, Kienzle G: Variable velocity 2-D phase contrast MR angiography for the identification of intracranial slow flow states (abstract), in Book of abstracts, Society of Magnetic Resonance in Medicine, 9th annual meeting, New York, 1990, p 333 26. DeMarco JK, Dillon WP, Halbach VV, Tsuruda JS: Dural arteriovenous fistulas: Evaluation with MR imaging. Radiology 1990; 175:193-199 27. Lewin JS, Laub G: Evaluation of the intracranial venous system with the thin-slice oblique acquisition sequential technique. Presented at the 8th annual meeting, Society for Magnetic Resonance Imaging, Washington, DC, Feb 18-24, 1990 28. Creasy JL, Price RR, Presbey T, Goins D, Partain CL, Kessler RM: Gadolinium-enhanced MR angiography. Radiology 1990;175: 280-283 780 Stroke Vol 23, No 5 May 1992 29. Nadel L, Braun IF, Kraft KA, Jensen ME, Laine FJ: MRI of intracranial sinovenous thrombosis: The role of phase imaging. Magn Reson Imaging 1990;8:315-320 30. Nadel L, Braun IF, Kraft KA, Fatouros PP, Laine FJ: Intracranial vascular abnormalities: Value of MR phase imaging to distinguish thrombus from flowing blood. AJNR 1990;ll:1133-1140 31. Edelman RR, Mattle H, Kleenfield J, Silver MS: Quantification of blood flow with dynamic MR imaging and presaturation bolus tracking. Radiology 1989;171:551-556 32. Anderson CM, Saloner D, Tsuruda JS, Shapeero LG, Lee RE: Artifacts in maximum-intensity-projection display of MR angiograms.Atf? 1990;154:623-629 33. Meyer CH, Macovski A, Nishimura DG: Square spiral fast imaging. Presented at the 8th annual meeting, Society for Magnetic Resonance in Medicine, Amsterdam, The Netherlands, Aug 12-18, 1989 34. Lindskog ED, Haacke EM, Mitchell JD, Liang Z: Half-fourier imaging: A partially phase constrained iterative reconstruction scheme and an evaluation of several fast reconstruction schemes. Presented at the 8th annual meeting, Society for Magnetic Resonance in Medicine, Amsterdam, The Netherlands, Aug 12-18, 1989 35. Jackson JI, Meyer C, Nishimura DG, Macovski A: Projection reconstruction with a twist. Presented at the 9th annual meeting, Society for Magnetic Resonance in Medicine, New York, Aug 18-24, 1990 36. Masaryk TJ: MR angiography in cerebrovascular disease (course), in Book of abstracts, Radiological Society of North America, 76th annual meeting, Chicago, 1990, p 202 37. Chew WM, Tsuruda JS: Advantages of high resolution MR angiographic imaging, in Book of abstracts, Radiological Society of North America, 76th annual meeting, Chicago, 1990, p 1025 Downloaded from http://stroke.ahajournals.org/ by guest on May 6, 2017 Magnetic resonance angiography. Cerebrovascular applications. P M Ruggieri, T J Masaryk and J S Ross Stroke. 1992;23:774-780 doi: 10.1161/01.STR.23.5.774 Downloaded from http://stroke.ahajournals.org/ by guest on May 6, 2017 Stroke is published by the American Heart Association, 7272 Greenville Avenue, Dallas, TX 75231 Copyright © 1992 American Heart Association, Inc. All rights reserved. Print ISSN: 0039-2499. 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