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1 c nodules with subfoci of HCC, hyperintense, hypointense.
2 high-grade dysplastic nodules, hyperintense, hypointense.
3 c low-grade dysplastic nodules, hypointense, hypointense.
4 low-grade dysplastic nodules, hyperintense, hypointense.
5 version recovery hyperintense (18 of 18), T1-hypointense (17 of 18), and diffusion-hyperintense (15 o
6 /- 12, and 238 msec +/- 17, respectively) or hypointense (296 msec +/- 27, 163 msec +/- 12, and 199 m
7 isointense (8.5/s vs 9.5/s, p=0.02) and T(1) hypointense (7.7/s vs 9.5/s, p=0.003) compared with NAWM
8 66 from lesions on T2-weighted MR images (43 hypointense and 23 isointense on T1-weighted MR images),
14 and at the external surface of the cortex, a hypointense band deeper in the cortex, and a hyperintens
17 r MR imaging parameters, including number of hypointense brain lesions on T1-weighted MR images, pres
22 "Bagel Sign" pattern: a central lesion with hypointense core and hyperintense rim with or without co
30 contrast than adjacent normal prostate, and hypointense features on T2-weighted imaging; these findi
31 e defined as discrete, well-defined markedly hypointense foci within the adnexal lesion on T2-weighte
32 mall HCC, hyperintense, hypointense (n = 7); hypointense, hyperintense (n = 2); hyperintense, hyperin
34 ocardial hemorrhage was taken to represent a hypointense infarct core with a T2* value of <20 ms.
36 ganglion cell, and inner nuclear layer; the hypointense layer 2, the outer nuclear layer and the inn
38 tense lesion volume [T2LV]), the ratio of T1 hypointense lesion volume [T1LV] to T2LV [T1:T2]), brain
39 d tiw versus DT (nominal p<0.001); T2 and T1 hypointense lesion volume change was lower for sc IFN be
42 in T(1) isointense (44.6 +/- 7.2 mM) and T1 hypointense lesions (46.8 +/- 8.3 mM) compared with norm
44 of lateral ventricles, Dawson's fingers, T1 hypointense lesions (multiple sclerosis), fluffy lesions
45 lesions (all P<0.001) and new T(1)-weighted hypointense lesions (P<0.001, P<0.001, and P=0.002, resp
46 ns (both BG-12 doses), and new T(1)-weighted hypointense lesions (thrice-daily BG-12) (nominal P<0.05
47 er sodium concentration was observed in T(1) hypointense lesions in secondary-progressive (49.0 +/- 7
48 ection of blood-brain barrier break down and hypointense lesions on T1-weighted images, magnetization
49 1 mL, p=0.024) and a higher number of new T1-hypointense lesions over 0-12 months (p=0.005) as well a
50 mbers of new T2, gadolinium-enhancing and T1 hypointense lesions were lower with sc IFN beta-1a qw (n
51 imaging with ultra-highfield MRI that phase hypointense lesions were significantly more prevalent in
52 radient-recalled-echo MR images demonstrated hypointense lesions with variable contrast material enha
57 rast-to-noise ratio between hyperintense and hypointense liver regions, coefficient of variation, and
58 ic analysis; at MR imaging, PTLD appeared as hypointense masses on T1-and T2-weighted images with min
59 For both diseases, T1-weighted images showed hypointense masses with progressive enhancement (differe
61 ted images, respectively: HCC, hyperintense, hypointense (n = 3); hyperintense, hyperintense (n = 1);
63 hyperintense areas on T1-weighted images and hypointense on fat-suppressed T1-weighted images, compat
64 ntrifugal DCE lesions appeared isointense or hypointense on phase images, whereas centripetal DCE les
66 intrathoracic and subcutan masses as mainly hypointense on T1-weighted images and hyperintense on T2
67 te depiction of IRE ablation zones that were hypointense on T1-weighted images and hyperintense on T2
68 eatures were the following: all lesions were hypointense on T2- and hyperintense (n=12) and isointens
70 lesions that shrink least and become more T1 hypointense over time suggests that the rim might mark f
72 whereas centripetal DCE lesions showed thin, hypointense phase rims that clearly colocalized with the
73 ic lesions also selected for the presence of hypointense phase rims, the findings were stable over ti
76 oxide nanoparticles are detected in vivo as hypointense regions in the liver up to two weeks post in
77 ADC threshold, (ii) visual determination of hypointense regions on ADC maps, and (iii) visual determ
78 ice that received labeled cells demonstrated hypointense regions within the tumor that evolved over t
79 Fibroids were classified as hyperintense or hypointense relative to skeletal muscle on pretreatment
80 APAs (mean size, 20 x 16 mm) were iso- or hypointense relative to the liver on T1-weighted images
84 elected for treatment had no hyperintense or hypointense signal intensity changes on the DW images or
85 sence of fluid collection with isointense or hypointense signal on T1-weighted images, fluid-equivale
87 categorized into four subgrades: subgrade A, hypointense; subgrade B, inhomogeneous; subgrade C, hype
88 antified on a three-point ordinal scale (0 = hypointense to brain parenchyma, 1 = isointense to brain
90 ced more than metastases, they also remained hypointense to liver on T1-weighted images (from -4.87 +
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