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1 was randomized (136 subclavian vein and 134 femoral vein).
2 tinuous exposure to flowing blood within rat femoral vein.
3 oxide in a manner similar to that of porcine femoral vein.
4 denosine 140 mcg/kg per minute via a central femoral vein.
5 ges acquired within the pump circuit and the femoral vein.
6 ioMEMS) is approved for implantation via the femoral vein.
7 of the right superficial femoral artery and femoral vein.
8 ) in PBS or a PBS-alone injection into right femoral vein.
9 We infused hyperosmolar sucrose via the femoral vein.
10 ization of the right femoral artery and left femoral vein.
11 heter with a snare introduced via the common femoral vein.
12 atic or asymptomatic DVT in the popliteal or femoral veins.
13 elial cells or endothelial cells of isolated femoral veins.
14 Two 8-Fr catheters were placed into the femoral veins.
15 ers inserted in the brachial artery and both femoral veins.
16 vigation-guided mapping/ablation with normal femoral vein access (49); and Group C, remote magnetic n
18 eight healthy volunteers once with bilateral femoral vein and artery catheters during a 3-h basal per
22 uptake and definitive in vivo images of both femoral vein and pulmonary thrombi show that 99mTc-P748
23 catheters were surgically implanted into the femoral vein and sepsis was induced by cecal ligation an
26 operator characteristics analyses were 0.76 (femoral vein) and 0.77 (popliteal vein) based on inciden
27 e, sampling (artery and portal, hepatic, and femoral veins) and infusion (vena cava, duodenum) cathet
28 rosal sinus, and the internal jugular vein), femoral vein, and radial artery of patients undergoing i
31 othelial cells and when placed into isolated femoral vein as well as increased endothelial cell monol
33 es were taken from the LA, right atrium, and femoral vein at baseline and at 15 min in all 3 groups.
34 ariable Cox regression model, postthrombotic femoral veins at baseline (hazard ratio, 2.64 [95% CI, 1
38 They underwent tracheostomy, jugular and femoral vein cannulation, femoral artery cannulation, ca
39 ture suggest that thrombosis associated with femoral vein catheterization should be considered when c
40 of a heretofore undescribed complication of femoral vein catheterization, phlegmasia cerulea dolens
42 mon femoral vein (CFV), proximal superficial femoral vein (CFV), mid-SFV, distal SFV, and popliteal v
43 s were categorized at five locations: common femoral vein (CFV), proximal superficial femoral vein (C
44 n alone as a placebo by injection into right femoral vein, directly into the left ventricular (LV) ca
45 Glutathione also elevated cGMP levels in the femoral vein during ACH infusion from 17.6 +/- 3 to 23.3
46 ) was infused over the next 3 min of CPR via femoral vein followed by up to three defibrillation atte
48 The animals had a catheter inserted into the femoral vein for administration of 5-HT (0.00375 mg) and
49 proach (femoral artery diagnostic access and femoral vein for temporary pacing lead placement) for se
50 serted either in the internal jugular or the femoral vein had greater risk to be colonized than cathe
52 cs on blood from artery, coronary sinus, and femoral vein in 110 patients with or without heart failu
54 ed into the subclavian, internal jugular, or femoral vein in two randomized trials during 1998-2000 w
55 re unit (ICU) to the subclavian, jugular, or femoral vein (in a 1:1:1 ratio if all three insertion si
57 erval [0.30-0.70], I=0%; subclavian vein vs. femoral vein, incidence density ratio 0.27; 95% confiden
58 type second harmonic ultrasound system after femoral vein injection of AF0145 (10 to 40 mg) in 13 clo
61 Animals are first anesthetized, then one femoral vein is exposed and subjected to a standardized,
65 subclavian, 3053 internal jugular, and 1554 femoral vein) met the inclusion criteria, one of which w
66 ale Swiss mice after femoral artery (n = 7), femoral vein (n = 6) or intraperitoneal (n = 6) injectio
69 red, and changes in leg blood flow (LBF) and femoral vein nitric oxide nitrite plus nitrate (NOx) flu
70 genic injury was subsequently induced in the femoral vein of each mouse and the area (size) of thromb
73 inetics of thrombus formation induced in the femoral veins of the experimental mice were compared.
74 ion at rest, (3) passive exercise (n=10), (4)femoral vein or artery ATP infusion (n=6), and (5) cycli
79 rine administration via the right atrium and femoral vein resulted in significant increases in plasma
80 ery, vena cava, portal vein, femoral artery, femoral vein, saphenous vein, pulmonary vein, and pulmon
81 ous conduits must be utilized, cryopreserved femoral veins seem to provide superior patency rates.
83 l, vaginal mucosa, and clitoris assessments; femoral vein signal intensity measurements; relative reg
84 e inferior vena cava, iliac veins, or common femoral vein successfully treated with venous stent plac
85 amples were obtained simultaneously from the femoral vein (systemic sample) and the coronary sinus (l
86 of peak oxygen uptake while leg blood flow (femoral vein thermodilution), mean arterial blood pressu
88 and purity and provided definitive images of femoral vein thrombi within 20 min and pulmonary thrombi
89 ical and yield purity and provided images of femoral vein thrombin in the canine model by 1 hr postin
91 eous entry into the abdominal aorta from the femoral vein through the adjoining inferior vena cava.
94 utive adults with cancer underwent bilateral femoral vein ultrasonography on admission and weekly unt
98 lood samples from the coronary sinus and the femoral vein were collected at those time points and the
99 ein thrombosis involving the iliac or common femoral veins were randomized to PCDT with anticoagulati
100 atheters inserted in the internal jugular or femoral veins when catheters are not used for drawing bl
101 Biopsies were performed via the ipsilateral femoral vein with a renal biopsy set designed for transj
102 the brachial artery and internal jugular and femoral veins with plasma and RBC nitric oxide metabolit
103 m cannulae in the inferior vena cava and the femoral veins, with a tie on the inferior vena cava sepa