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1 ed with a site in the appendicular skeleton (humerus).
2  differences were not detected in the distal humerus.
3 nts with displaced fractures of the proximal humerus.
4 magnetic resonance (MR) imaging of the right humerus.
5 d we apply this pipeline to the regenerating humerus.
6 ns frequently affected the femur, tibia, and humerus.
7 l and endosteal surfaces of the mandible and humerus.
8 resented by only a proximal femur and distal humerus.
9                With a powerfully-constructed humerus 1.76 m in length, Notocolossus is one of the lar
10 empts were made into either the tibia or the humerus; 192 were unsuccessful, with an overall success
11 ania from Myanmar, including a complete left humerus, a fragmentary right humerus, parts of left and
12 ris tendon from the lesser tuberosity of the humerus, accompanied by medial dislocation of the biceps
13                                            A humerus and a femur belong to larger hadrosaurids, ~ 6 m
14  to the base of the medial epicondyle of the humerus and distally to the medial aspect of the coronoi
15 t were drawn around the head and neck of the humerus and femur (both sides) and around lumbar vertebr
16 m in patterns of growth, but the size of the humerus and femur diverges early in development.
17 fetal weight (EFW), head circumference (HC), humerus and femur lengths, abdominal circumference and a
18 kly growth pace as measured by fetal weight, humerus and femur lengths, and abdominal and head circum
19  the compound structures observed around the humerus and femur of Kulindadromeus are support fibers a
20                             In the stylopod (humerus and femur) and sternum, bone marrow MSCs express
21        The two-dimensional CNN model for the humerus and glenoid achieved a DSC of 0.95 and 0.86, a p
22                    The 3D CNN model, for the humerus and glenoid, achieved a DSC of 0.95 and 0.86, pr
23 ressed most indices of bone formation in the humerus and mandible, while NE decreased some indices of
24 and second moments of area of the mid-distal humerus and midshaft femur.
25  periosteal and endocortical surfaces of the humerus and the periosteal and cancellous bone surfaces
26 lable for three different bone sites (femur, humerus and tibia), very little variation with bone site
27 gnificantly induced the loss of bone mass on humerus and tibia, compared with artificial 1G induced b
28                                          The humerus and ulna indicate that Pondaungia was capable of
29 croarchitecture in weight bearing (femur and humerus) and non-weight bearing (2(nd) lumbar vertebra a
30 cipally located in the tibia, femur, pelvis, humerus, and spine and, in most cases, presented the ima
31 hat evolutionary changes in the shape of the humerus are driven by ecology and phylogeny and are asso
32  of the lower limb bones and strength of the humerus are much smaller and less consistent.
33  prototype to image the surface of the human humerus at different positions along the arm, demonstrat
34 oreover, the preservation of a crocodyliform humerus between the dentaries of the new theropod may pr
35 plied to the study of human bones (femur and humerus) burned simultaneously under either aerobic or a
36 greater bone volume fraction relative to the humerus, but other aspects of trabecular architecture ar
37        At 4 wk of implantation in the rabbit humerus, control-released TGF-beta1 from porous implants
38 ern blot of human osteoclastoma or fetal rat humerus demonstrated bands of 38 and 27 kDa, consistent
39  or stage 27 chick embryos severely affected humerus development.
40 sis of non-pathological fracture of the hip, humerus, distal tibia, wrist, or vertebrae between Octob
41  Smaller body size was not a risk factor for humerus, elbow, wrist ankle, or foot fractures.
42 clinical trial, the Proximal Fracture of the Humerus Evaluation by Randomization (PROFHER) trial, rec
43 s present in stage 27 (Day 5.5) chick embryo humerus exhibited low and diffuse expression of RARalpha
44   Experiment on the ground, the bone mass of humerus, femur and tibia was measured using micro-comput
45 tant embryo has four limbs with recognizable humerus/femur bones that have anterior-posterior polarit
46 mode to consistently show increased rates of humerus/femur morphological evolution.
47 2-year follow-up of the Finnish Shaft of the Humerus (FISH) randomized clinical trial comparing surge
48 incidence of nonvertebral fracture (proximal humerus, forearm, hip) in adult kidney transplant recipi
49 primary outcome was a composite end point of humerus, forearm, pelvis, or hip fracture requiring inte
50             Subsequent evolution of synapsid humerus form and functional traits showed little evidenc
51 t problems, increased the odds of a proximal humerus fracture (adjusted odds ratio = 1.65, 95% confid
52          This case-control study of proximal humerus fracture included 448 incident female and male c
53 ional study included infants with a femur or humerus fracture or both undergoing abuse evaluation at
54  aged younger than 12 months with a femur or humerus fracture or both without overt signs or symptoms
55 ocused on anterior cruciate ligament repair, humerus fracture repair, cholecystectomy, posterior spin
56 ; P = .003), fracture type (OR for femur and humerus fracture vs isolated femur fracture, 5.36; 95% C
57 prescription and probability of a refill for humerus fracture, spinal fusion, and tonsillectomy.
58 lopia, osteoarthritis, epidural haemorrhage, humerus fracture, subdural haemorrhage, and tibia fractu
59 ould likely reduce the frequency of proximal humerus fracture.
60 h a higher risk of frailty (hip and proximal humerus) fractures but not fractures at other sites.
61 tic (hip, pelvis, spine, wrist, and proximal humerus) fractures individually and any fracture in thos
62                                   A tetrapod humerus from the Late Devonian of Pennsylvania has a nov
63 utomatically classify nine anatomical terms: humerus, handplate, fibula, tibia, femur, ribs, petrous
64 ransition(1-9), an isolated bone, a putative humerus, has controversially hinted at a wider range in
65 ultrasonography to determine femur (FLZ) and humerus (HLZ) length z scores.
66 enoids: ICC, 0.26; supracondylar fracture of humerus: ICC, 0.25; cleft lip and palate: ICC, 0.24; acu
67 ve the radial head in adults, and the distal humerus in children.
68 We quantified morphological disparity of the humerus in pelycosaur-grade synapsids and therapsids usi
69 arise until loss of the ancestral 'L-shaped' humerus in the crown group, setting the stage for the di
70 taining a displaced fracture of the proximal humerus involving the surgical neck.
71                                     An adult humerus is estimated to be 9 - 16% shorter and thinner t
72                          Its 1.69-meter-long humerus is longer than that of any known Cretaceous saur
73 mparisons show that the overall shape of the humerus is more similar to that of echidnas than the pla
74 ghtly larger size, the Arctic presbyornithid humerus is not distinguishable from fossils of Presbyorn
75 scapularis from the lesser tuberosity of the humerus is rare in the pediatric population and only a c
76                                    Moreover, humerus length and bone mineral content were decreased,
77 tal head circumference, biparietal diameter, humerus length, abdominal circumference, femur length an
78 7 wk was associated with increased femur and humerus lengths at 28 wk.Maternal weight gain was associ
79  characters including restricted mobility in humerus long-axis rotation, increased muscular leverage
80 d radiations was accompanied by variation in humerus morphofunctional traits.
81 al tibia (n = 7), distal radius and proximal humerus (n = 3), and calcaneus and public ramus (n = 2).
82 orearm (n = 1,000), foot (n = 827), proximal humerus (n = 448), shaft of the tibia/fibula (n = 168),
83 orearm (n = 1,016), foot (n = 574), proximal humerus (n = 467), pelvis (n = 150), and shaft of the ti
84 femur (n = 17; 50%), tibia (n = 9; 26%), and humerus (n = 5; 15%).
85     The lesions were located in the proximal humerus (n = 7), proximal tibia (n = 4), proximal femur
86 s of extant cetaceans, including a shortened humerus, narrow peduncle, and loss of radial tuberosity,
87 ur but had no effect on cortical bone in the humerus or calvarium.
88 oward specific skeletal elements such as the humerus or digits.
89                         Of 2585 infants with humerus or femur fracture or both undergoing evaluations
90 orphometric indices of bone formation in the humerus or mandible.
91         A primary tumor site in the proximal humerus or proximal femur and an elevated serum alkaline
92 mary outcome was nonvertebral fracture (hip, humerus, or radius or ulna) within 12 months of treatmen
93  with a first diagnosed fracture of the hip, humerus, or wrist; up to 4 controls, matched by age, sex
94 a complete left humerus, a fragmentary right humerus, parts of left and right ulnae, and the distal h
95 muscle activity at the primary movers of the humerus (pectoralis major (PM), anterior (AD) and poster
96 -trauma fracture of the hip, spine, proximal humerus, pelvis, and/or wrist, requiring surgery.
97  were included with individual assessment of humerus, radius, and ulna (69 bones; 36 fractured).
98 fracture, hip fracture requiring surgery, or humerus, radius, or ulna fracture requiring intervention
99                        Risk for pelvic, hip, humerus, radius, ulna, carpal, metacarpal, metatarsal, o
100 al: 0.99, 2.04) and fracture of the proximal humerus (rate ratio = 1.79, 95% confidence interval: 1.0
101 90, Recall:0.97, Cohen's kappa: 0.85) in the humerus region.
102 utionary adaptive landscapes to integrate 3D humerus shape and functional performance data across a t
103 luate standard bone parameters in the tibia, humerus, sternebra, vertebrae, ribs, calvarium, mandible
104     The morphology of a large well-preserved humerus supports identification of a new volant, possibl
105 Adult Keichousaurus males have a more robust humerus than females, with pronounced muscle attachment
106 T-PCR revealed a higher turnover rate in the humerus than in lumbar vertebrae, suggesting enhanced bo
107 trongly expressed in the proximal end of the humerus than the distal end.
108 ced a nonadaptive correlated response in the humerus that overwhelmed its own trait-specific response
109 cadburyi, currently only known from a single humerus, that provides key information relating to this
110 re complex featherlike structures around the humerus, the femur, and the tibia.
111 tern was femur (OR, 20.6; 95% CI, 8.4-48.1), humerus, then vertebra/ribs.
112 st fracture was a comminuted fracture of her humerus three years ago, when she stumbled and fell forw
113 les of the upper arm and was anchored to the humerus through osseointegration, the process in which b
114 mb patterning along the proximo-distal axis (humerus to digits).
115 iceps brachii muscle tendon and connects the humerus to the ulna.
116 d gradient-echo in vivo images of the femur, humerus, upper spine, and lower spine were acquired for
117 cation of tumour (proximal femur or proximal humerus vs other limb vs axial skeleton); and presence o
118        The shaft cortical thickness of their humerus was measured using a 3D morphometric mapping app
119 ntradiction to ecogeographic hypotheses, the humerus was under directional selection for longer value
120 y positively associated with fetal femur and humerus z scores (P < 0.01).
121                              Fetal femur and humerus z scores and neonatal birth length were signific
122  25(OH)D was associated with fetal femur and humerus z scores only when maternal calcium intake was <
123  times across gestation, and fetal femur and humerus z scores were generated.

 
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