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1 ight of or over the spinous processes of the vertebral body.
2 terior elements, with partial involvement of vertebral body.
3 mount of polymethylmethacrylate injected per vertebral body.
4 tion of inflatable bone tamps (IBT) into the vertebral body.
5 located on the anterolateral surface of the vertebral body.
6 rienced relapse, with painful collapse of L3 vertebral body.
7 ance in 1984 due to a hemangioma of cervical vertebral body.
8 d the destruction of the anterior rim of the vertebral body.
9 y fractures and liquefactive necrosis of the vertebral body.
10 n the midline to the posterior aspect of the vertebral body.
11 n the intervertebral disc accumulates in the vertebral body.
12 protein from the intervertebral disc to the vertebral body.
13 iffuse away from its place of synthesis, the vertebral body.
14 anterolateral spinal column at four adjacent vertebral bodies.
15 ocytic cells of presumptive inner annuli and vertebral bodies.
16 narrowing, and anterior wedging of involved vertebral bodies.
17 c space and permanent fusion of the adjacent vertebral bodies.
18 n the craniofacial structures but not in the vertebral bodies.
19 evel of the fifth, eighth, and 10th thoracic vertebral bodies.
20 Each site may involve up to 2 contiguous vertebral bodies.
21 ral alterations in the adjacent NP cells and vertebral bodies.
22 f 98.3% for the differentiation of edematous vertebral bodies.
23 ed to well-segmented areas of the developing vertebral bodies.
24 n infusion of donor BM cells isolated from 9 vertebral bodies.
25 gth and stiffness in both the tibiae and the vertebral bodies.
26 facial cartilage, heart, bronchi, kidney and vertebral bodies.
27 5/8 phosphorylation was decreased in CV2(-/-)vertebral bodies.
28 terally within the thoracic and lumbar spine vertebral bodies.
29 V2 protein is normally located in the future vertebral bodies.
30 ating sclerotomal cells that form the mature vertebral bodies.(4) Previous work demonstrated that not
31 diameter at the aortic arch, carina, and one vertebral body above the gastroesophageal junction was 1
32 epidural empyemas, abscess between adjacent vertebral bodies, abscesses beneath anterior longitudina
34 rning defects that included fusions of ribs, vertebral bodies and abnormal formation of spinous proce
36 bris, and gadolinium-enhancement patterns of vertebral bodies and disks may help differentiate spinal
37 l skeleton consists of a metameric series of vertebral bodies and intervertebral discs, as well as ad
39 o rapidly measure morphometric quantities in vertebral bodies and output LLAs across multiple modalit
40 from both somitic mesoderm, which forms the vertebral bodies and ribs, and from lateral plate mesode
43 f occult vertebral body and facet fractures, vertebral body and facet contusions, intervertebral disk
44 dent readers assessed the presence of occult vertebral body and facet fractures, vertebral body and f
46 f the abdominal aorta at the level of the L3 vertebral body and its associations with multiple variat
47 ed diffuse bony involvement including the T7 vertebral body and left pedicle, ribs, pelvis, and calva
48 Lytic disease involving more than 40% of the vertebral body and location at or below T10 confer a hig
50 of spinal deformity, the position of the C7 vertebral body and sacrum remain within the 95% confiden
51 rst from intervertebral spaces and then from vertebral bodies, and it progressively underwent apoptos
52 imarily in the anterosuperior portion of the vertebral body, and cleft margins appeared increasingly
54 roplasty, long-term outcome of cement in the vertebral body, and utility of prophylactic vertebroplas
58 The purpose of the IBT is to restore the vertebral body back toward its original height, while cr
59 lgorithm, can measure three-dimensional (3D) vertebral body BMD across consistently imaged thoracic l
61 ficity, and area under the curve of DECT for vertebral body BME were 89% (95% CI: 84%, 92%), 96% (95%
62 ecipients infused perioperatively with donor vertebral body bone marrow (DBMC-i) vs. 219 noninfused c
64 leen cells in the presence of specific donor vertebral-body bone marrow cell (DBMC) modulators were t
65 populations were isolated from cadaver donor vertebral-body bone marrow cells (DBMC) by using immuno-
69 metameric structure composed of alternating vertebral bodies (centra) and intervertebral discs.(1) R
71 vertebral body (P<.01), and continuation of vertebral body changes with posterior pharyngeal wall ul
73 rvening joint change (P<.001), more cases of vertebral body collapse (P<.01), more bilateral symmetri
75 DXA, 39 (48%) of 81 patients with unreported vertebral body compression fractures had a nonosteoporot
77 iewed for the presence of moderate or severe vertebral body compression fractures of the lower thorac
81 The resulting reinforcement of the fractured vertebral bodies eliminated the pain and the need for na
82 able to depict bone marrow in the collapsed vertebral bodies, especially in those with less than 50%
83 vertebral bodies, severe destruction of the vertebral body, focal/heterogeneous contrast enhancement
86 ression of CDMP-1 in the notochord inhibited vertebral body formation by blocking migration of sclero
87 , one person was diagnosed with pathological vertebral body fractures and liquefactive necrosis of th
90 er system detects and anatomically localizes vertebral body fractures in the thoracic and lumbar spin
91 ith positive findings for fractures (59 with vertebral body fractures) and 10 control examinations (w
94 BMD were performed by QCT analysis for each vertebral body from T12 to L5, and mean BMD was calculat
96 educe pain and further collapse and/or renew vertebral body height by introducing bone cement into fr
98 ections, bone marrow signal changes, loss of vertebral body height, abnormal signal in intervertebral
99 The statistical significance of changes in vertebral body height, wedge angle, and weight with the
103 focal/heterogeneous contrast enhancement of vertebral bodies, heterogeneous signal from the vertebra
104 f vertebral bodies, low-grade destruction of vertebral bodies, hyperintense/homogeneous signal from t
105 sk R-CNN, to automatically segment and label vertebral bodies in lateral cervical and lumbar spinal X
107 hod and using the activity concentrations in vertebral bodies in SPECT images at 24 h after injection
109 ed at or below the level of the third sacral vertebral body in all 49 patients with isolated pelvic f
111 CT appearance, lesion location, and percent vertebral body involvement independently predicted fract
113 tebra is human-like in overall shape but its vertebral body is somewhat intermediate in shape between
116 ral network model was then trained to output vertebral body landmarks for vertebral height measuremen
118 diffuse/homogeneous contrast enhancement of vertebral bodies, low-grade destruction of vertebral bod
122 and in a phantom model, visualization of the vertebral body marrow was improved and susceptibility ar
125 o independent readers visually evaluated all vertebral bodies (n = 163) for the presence of abnormal
127 measure bone density of thoracic and lumbar vertebral bodies on computed tomographic (CT) images.
128 images, diffuse signal intensity patterns in vertebral bodies on MR images, and rim enhancement of di
129 tebral bodies, heterogeneous signal from the vertebral bodies on T2 TIRM images, well-defined paraspi
131 e location was related to that of a thoracic vertebral body on frontal and lateral chest radiographs
132 ssiveness, spinal level, location within the vertebral body or posterior elements, involvement of sof
133 e IRE electrode to the posterior wall of the vertebral body or the exiting nerve root were 2.93 mm +/
134 , each consisting of two key components: the vertebral body (or centrum) and the vertebral arches.
135 te cancer cells were either coimplanted with vertebral bodies, or inoculated in the tibiae of immunoc
136 Paraspinous fluid collections and discitis/vertebral body osteomyelitis simulating pyogenic infecti
137 more bilateral symmetric involvement of the vertebral body (P<.01), and continuation of vertebral bo
138 acture (P<.01), bone marrow contusion of the vertebral body (P=.01), muscle strain (P<.01) or tear (P
139 e- and postoperative HU were measured at the vertebral body, pedicle, and spinal cord at three differ
140 Romanus lesions (RLs) and end-plate, diffuse vertebral body, posterior element, and spinous process b
142 ry tests data) and CT images covering lumbar vertebral bodies rather than DXA data via machine learni
143 the torso, defined as the position of the C7 vertebral body relative to the sacrum in a 'birds eye vi
144 toff value of -80 to differentiate edematous vertebral bodies resulted in a sensitivity of 96.3%, spe
145 cant changes in the images of bone marrow in vertebral body scans; with a decrease in the intensity o
146 trated significantly improved performance in vertebral body segmentation and labeling for spinal X-ra
148 d bone marrow edema on STIR images from each vertebral body, separately identifying central and later
149 cic spine, involvement of 2 or more adjacent vertebral bodies, severe destruction of the vertebral bo
151 .19, 0.34) and between a type 1 endplate and vertebral body spondylolisthesis (PPV, 0.28; 95% CI: 0.2
153 NAT was measured at the level of the C5 vertebral body, subdivided into posterior (NATpost), sub
155 icant differences in HU were observed at the vertebral body, the pedicle, and the spinal cord at the
156 and the ubiquitous osteochondrodysplasia of vertebral bodies to the occasional sarcoma in older anim
157 rument could be navigated into the posterior vertebral body tumors with a transpedicular approach.
158 47 tumors) with painful metastatic posterior vertebral body tumors, some of which were radiation ther
159 was assessed by the Hounsfield Unit (HU) in vertebral bodies (VB) and pedicles with and without cort
160 ssed at CT at the level of the 12th thoracic vertebral body via semiautomated threshold-based segment
161 ing penumbra, and bone marrow from the L3-L5 vertebral bodies was contoured on pretreatment FDG PET/C
164 furcation and duodenal papilla from adjacent vertebral bodies was measured on 34 cholangiograms, and
166 ion, and morphology of the tibiae and lumbar vertebral bodies were assessed by micro-computed tomogra
171 s of transgenic mice were tougher, and their vertebral bodies were stiffer and stronger than those of
176 painful bone metastases, excluding skull and vertebral bodies, were enrolled in a prospective open-la
177 wer chondrogenic cells within the developing vertebral body, which fail to condense appropriately alo
181 98.2%, and accuracy of 97.6% in the group of vertebral bodies with less than 50% sclerosis and/or air
183 moderate amounts of PMMA may escape from the vertebral body with no significant effect on therapeutic