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1 our times higher than that with conventional fast spin-echo (0.12) and gradient-echo (0.19) MR imagin
2 itivity and specificity of three-dimensional fast spin-echo (3D FSE) MRC for the evaluation of biliar
3                                              Fast spin-echo anatomic images were obtained, followed b
4          We used T2-weighted two-dimensional fast spin echo and T1-weighted three-dimensional magneti
5  Breath-hold coronal T2-weighted single-shot fast spin-echo and breath-hold coronal 3D T1-weighted sp
6 d ablated tissue was imaged with T2-weighted fast spin-echo and contrast-enhanced T1-weighted gradien
7 CC who underwent T2-weighted conventional or fast spin-echo and gradient-echo (GRE) (echo time > or =
8 tive freehand MR guidance predominantly with fast spin-echo and gradient-echo sequences.
9 specimens, and investigated with T2-weighted fast spin-echo and multiecho spin-echo sequences on a 3.
10 nts were imaged with endovaginal T2-weighted fast spin-echo and single-shot DW echo-planar MR imaging
11 (MR) images (including intermediate-weighted fast spin-echo and T2 mapping sequences), and the Physic
12 od and via water-saturation efficiency using fast spin-echo and T2-weighted images.
13 prepared RAGE sequence, as compared with the fast spin-echo and TOF sequences, demonstrated higher di
14 d-attenuated inversion recovery, T2-weighted fast spin-echo, and T2*-weighted gradient-echo sequences
15 ination of gradient-echo and high-resolution fast-spin-echo axial pulse sequences were used.
16   T(2) and Mo(*) maps were also created from fast spin echo data in a subset of pigs (n=5) to help ch
17 ptic nerves were imaged with a fat-saturated fast spin echo (FSE) sequence and a magnetization transf
18 agittal fat-suppressed intermediate-weighted fast spin-echo (FSE) (repetition time msec/echo time [TE
19 tra-low-SAR optimized three-dimensional (3D) fast spin-echo (FSE) and fluid-attenuated inversion-reco
20 weighted gradient-echo (GRE) and T2-weighted fast spin-echo (FSE) MR imaging before and after SPIO en
21 mpare a new isotropic three-dimensional (3D) fast spin-echo (FSE) pulse sequence with parallel imagin
22 MR imaging by using morphologic (T1-weighted fast spin-echo [FSE], T2-weighted FSE, proton density [P
23                     Conventional T2-weighted fast spin-echo (hydrogen) images were also obtained to d
24 c resonance scans, including oblique coronal fast spin echo images of the temporal lobes; [18F]fluoro
25 le, 55 degrees ) and T2-weighted single-shot fast spin-echo images (1501/80) were acquired.
26 sion was measured on T2-weighted single-shot fast spin-echo images by one of six radiologists (1-3 ye
27        Measurements were made on single-shot fast spin-echo images by tracing free-form regions of in
28 d-lesion contrast on T2-weighted breath-hold fast spin-echo images improves after administration of a
29 c lesions, identical T2-weighted breath-hold fast spin-echo images were obtained before and after gad
30  axial T1-weighted spin-echo and T2-weighted fast spin-echo images were obtained in all patients.
31        T1-weighted spin-echo and T2-weighted fast spin-echo images were obtained.
32 anced, and respiratory-triggered T2-weighted fast spin-echo images.
33  fast gradient-recalled echo and T2-weighted fast spin-echo images.
34 g transverse relaxation were generated using fast spin echo imaging.
35  parallel lines with enhanced reconstruction fast spin-echo imaging (T2 method), and gradient-echo im
36        Thus, gadolinium-enhanced T2-weighted fast spin-echo imaging also is expected to show negative
37 CP included thick- and thin-slab single-shot fast spin-echo imaging and transverse fast spin-echo ima
38 cluded T1-weighted spin-echo and T2-weighted fast spin-echo imaging in multiple planes with a phased-
39 e-shot fast spin-echo imaging and transverse fast spin-echo imaging.
40 on pulse was followed by acquisition through fast spin-echo imaging.
41 repared RAGE imaging; 70%, 92%, and 0.63 for fast spin-echo imaging; and 56%, 96%, and 0.57 for TOF i
42 several MR sequences: unenhanced T2-weighted fast spin-echo imaging; unenhanced diffusion-weighted im
43                MR imaging was fat suppressed fast spin echo intermediate or T2 weighted (repetition t
44 gnetization-prepared RAGE (kappa = 0.53) and fast spin-echo (kappa = 0.42) sequences yielded moderate
45 s reviewed subsecond T2-weighted single-shot fast spin-echo kidney MR imaging findings in 528 patient
46 ographically gated variable flip angle (VFA) fast spin-echo magnetic resonance (MR) angiography techn
47 aterial-enhanced, double inversion-recovery, fast spin-echo magnetic resonance (MR) images were acqui
48                            Three-dimensional fast spin-echo magnetic resonance images were acquired a
49 nic tumors underwent breath-hold single-shot fast spin-echo magnetic resonance imaging during a CO2 e
50 ectrocardiographically gated partial-Fourier fast spin-echo methods and balanced steady-state free pr
51                              A fast recovery fast spin echo MR sequence was selected for high RF powe
52                                  Single-shot fast spin-echo MR cholangiography is an accurate, noninv
53                                  Black-blood fast spin-echo MR images allow morphologic assessment of
54 ed use of moderately and heavily T2-weighted fast spin-echo MR images improves differentiation of sma
55                          Coronal T2-weighted fast spin-echo MR images in 30 neurologically normal pat
56 tive loss of signal intensity on T2-weighted fast spin-echo MR images obtained with fat saturation co
57 rmalities (n = 126) on intermediate-weighted fast spin-echo MR images were categorized into four subg
58             With use of sagittal single-shot fast spin-echo MR images, the cecal tilt angle was calcu
59        T1-weighted spin-echo and T2-weighted fast spin-echo MR imaging (5-mm-thick sections) were per
60 ation was correlated only with fat-saturated fast spin-echo MR imaging (r = 0.76, P < .01); the relat
61 ore accurately quantified with fat-saturated fast spin-echo MR imaging than with out-of-phase gradien
62  liver fat quantification with fat-saturated fast spin-echo MR imaging was significantly better than
63  studied with a T2-weighted, dual-inversion, fast spin-echo MR sequence.
64 nt T1-weighted gradient-echo and T2-weighted fast-spin-echo MR imaging at 1.5 T before and after intr
65                                              Fast-spin-echo MR venography allowed evaluation of slow-
66 ional area); (ii) optic nerve proton density fast spin-echo (optic nerve proton density-lesion length
67 pid imaging (fast spin-echo, water-selective fast spin-echo, or water-specific three-point Dixon grad
68                               Whole-brain 3D fast spin-echo pseudocontinuous ASL images were acquired
69 l T1rho-weighted images were obtained with a fast spin-echo pulse sequence for comparison.
70 mputed from images acquired by using a mixed fast spin-echo pulse sequence that was implemented with
71 magnetic resonance (MR) imaging with a mixed fast spin-echo pulse sequence were assessed.
72 (r = 0.813), followed by TOF (r = 0.745) and fast spin-echo (r = 0.497) imaging.
73 -weighted acquisition strategies-breath-hold fast spin-echo, rapid acquisition with relaxation enhanc
74                       Thick-slab single-shot fast spin-echo (repetition time msec/echo time msec, 4,5
75 ients, T1-weighted spin-echo and T2-weighted fast spin-echo sagittal MR images were retrospectively r
76 teady state (SPGR), and two-dimensional (2D) fast spin echo (SE)-for evaluating articular cartilage i
77  images and the fat-suppressed, T2-weighted, fast spin-echo (SE) images were reviewed in 19 patients
78 al (2D) single- and multisection black-blood fast spin-echo (SE) sequences.
79 gittal noncontiguous T2-weighted single-shot fast spin-echo (SE) sequences; transverse fat-suppressed
80                                  T1-weighted fast spin-echo (SE), fat-suppressed T2-weighted fast SE,
81  imaging sequences (an intermediate-weighted fast spin-echo [SE] sequence and a spoiled gradient-echo
82 rains were scanned with a diffusion-weighted fast spin echo sequence at 78 mum isotropic voxels.
83 ation of the needle tip was confirmed with a fast spin-echo sequence (1904/4.5, 36-cm field of view).
84                                          The fast spin-echo sequence and the fat-saturated SPGR seque
85 nce, a water excitation SPGR sequence, and a fast spin-echo sequence at 3.0 T and a fat-saturated SPG
86                                            A fast spin-echo sequence was modified to include a magnet
87                                            A fast spin-echo sequence weighted with a time constant th
88 ent MR imaging at 3 T, including a dual-echo fast spin-echo sequence, a T1-weighted volume sequence,
89 annel surface coil and a dynamic single-shot fast spin-echo sequence.
90 re obtained with a double-inversion-recovery fast-spin-echo sequence in a 1.5-T MR system.
91 A commercially available heavily T2-weighted fast-spin-echo sequence was optimized for MR venography
92                                              Fast spin-echo sequences (proton density-weighted and T2
93 he water excitation, fat-saturated SPGR, and fast spin-echo sequences at 3.0 T and the fat-saturated
94 resonance (MR) imaging unit with T2-weighted fast spin-echo sequences immediately after, as well as 2
95 ons were performed at 1.5 T with T2-weighted fast spin-echo sequences in multiple planes.
96 All MR examinations consisted of multiplanar fast spin-echo sequences with similar tissue contrast at
97 ighted spoiled gradient-echo and T2-weighted fast spin-echo sequences, three-dimensional very short T
98 with three-dimensional gradient-recalled and fast spin-echo sequences.
99 ansverse and coronal T2-weighted single-shot fast spin-echo sequences.
100 n-recovery, and sagittal T1- and T2-weighted fast spin-echo sequences.
101 ation, using three-dimensional T(2)-weighted fast-spin echo sequences, before doing invasive autopsy.
102                           For primary signs, fast spin-echo short inversion time inversion-recovery a
103 quisition of heavily T2-weighted single-shot fast spin-echo (SSFSE) images and three-dimensional (3D)
104 ality and speed improvements for single-shot fast spin-echo (SSFSE) with variable refocusing flip ang
105  heavily T2-weighted [TR 2000 ms; TE-200 ms] fast spin echo study in coronal and sagittal planes.
106 t-saturated (FS) and non-fat-saturated (NFS) fast spin-echo T1-weighted imaging (T1 method), FS and N
107 es and clinical results for conventional and fast spin echo T2-weighted imaging, fluid-attenuated inv
108  contrast material enhancement, spin-echo or fast spin-echo T2- and proton-density-weighted MR imagin
109 cysts by using axial and coronal single-shot fast spin-echo T2-weighted images obtained at 1.5 T.
110 al spin-echo T1-weighted MR images and axial fast spin-echo T2-weighted images were obtained.
111  and phased-array MR imaging (ie, unenhanced fast spin-echo T2-weighted imaging and gradient-echo T1-
112 ture was seen on only 10 of the spin-echo or fast spin-echo T2-weighted MR images of lesions.
113                The imaging protocol included fast spin-echo T2-weighted MR imaging, breath-hold DW ec
114 maging examinations included T1-weighted and fast spin-echo T2-weighted sequences.
115             MR imaging included T1-weighted, fast spin-echo T2-weighted, and immediate and delayed ga
116            MR imaging with a fat-suppressed, fast spin-echo, T2-weighted sequence demonstrated high-s
117                                Conventional, fast spin-echo, three-dimensional gradient-echo, and gad
118 arotid MR imaging, including two-dimensional fast spin-echo, three-dimensional time-of-flight (TOF),
119 ction, high-spatial-resolution, T2-weighted, fast spin-echo; three-dimensional, spoiled gradient-reca
120                               Rapid imaging (fast spin-echo, water-selective fast spin-echo, or water

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