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1 Vd/Vt is predictable from clinically available data.
2 Vd/Vt was calculated using the Enghoff modification of t
3 core, 13 +/- 3.4 vs. 7.7 +/- 0.8; p = .006) (Vd/Vt, 0.68 +/- 0.07 vs. 0.58 +/- 0.07; p = .009) (EVLWp
4 albumin = 25 g/day + (albumin 1 - albumin 2)(Vd)/days, where albumin 1 and 2 are the serum albumin co
5 of 22.8 hours (range, 24.1 to 30.6 hours), a Vd of 9.4 L (range, 4.4 to 19.5 L), and a CL of 0.32 L/h
9 ttle or no avoidance, strikingly, the Dm and Vd were not engaged, despite similar levels of activatio
14 l nucleus of the ventral telencephalic area (Vd), the teleost anatomical homologs of the mammalian am
15 max, volume of distribution/bioavailability (Vd/F), and elimination half-life (t(1/2)) were not diffe
16 ve undertaken a comparative study of six (D, Vd, Vv, Dm, Dl, Ppa) periventricular zones (PVZs) harbor
17 equation for Vd/Vt using the clinical data: Vd/Vt = 0.32 + 0.0106 (Paco2 - ETCO2) + 0.003 (RR) + 0.0
19 val (PFS) over bortezomib and dexamethasone (Vd) in patients with relapsed/refractory multiple myelom
20 , mean half-life and volume of distribution (Vd) in women were 15 days and 72 mL/kg, respectively, af
21 .0 to 80.0 hours), a volume of distribution (Vd) of 10.9 L (range, 3.1 to 34.5 L), and a clearance (C
22 S-BBBO increases the volume of distribution (Vd) of dye after CED administration, but results in a sh
24 eristic curve analysis indicated that EVLWp, Vd/Vt, and extravascular lung water (p = .0005, .009, an
25 rrection for partial volume effect, [11C]FMZ Vd in the body of the epileptogenic hippocampus was redu
26 of [11C]FMZ volume of distribution ([11C]FMZ Vd) obtained in 10 patients with refractory mTLE due to
27 in the [11C]FMZ volume of distribution (FMZ-Vd) before and after correction for partial volume effec
30 lerosis showed significant reductions of FMZ-Vd in the hippocampus contralateral to the side of the E
31 ts, significant unilateral reductions of FMZ-Vd were found in one of the three patients with bilatera
33 used to construct a predictive equation for Vd/Vt using the clinical data: Vd/Vt = 0.32 + 0.0106 (Pa
35 ent score, dead space-tidal volume fraction (Vd/Vt), and EVLWp were all significantly higher on day 1
36 rmacokinetic profile (F, 82%; t(1/2), 5.6 h; Vd, 0.694 L/kg) with good drug penetration in target tis
43 56 demonstrated PFS and OS improvements over Vd in RRMM patients regardless of their baseline renal f
46 text]co2, dead space to tidal volume ratio (Vd/Vt), and arterial to end-tidal CO2 difference were al
47 iate regions and part of the ventral region, Vd/Vc/Vi, and Vv) expressed high levels of AptCB1R trans
48 the serum sampling intervals, respectively; Vd is the volume of distribution (L); and days relates t
50 primary end point was pulmonary dead space (Vd/Vt) at 6 hours after esophagectomy or before extubati
51 The volume of distribution at steady-state (Vd(ss)) was 700 L/m2 and the clearance was 300 mL/min/m2
54 age was also negatively correlated with TCR Vd + Jd receptor diversity regardless of immune challeng
55 dorsal nucleus of the ventral telencephalon [Vd]), parts of the preoptic area (NPOmg and NPOpc), ento
57 hours, the Cmax was 2,549 +/- 291 ng/mL, the Vd was 3.97 +/- 0.95 L, and the Vd/kg was 0.05 +/- 0.01
58 rst characterization of an F. nucleatum Type Vd phospholipase class A1 autotransporter (strain ATCC 2
59 ct, track, and characterize the role of Type Vd secreted phospholipases in Gram-negative bacteria.
61 cies with high particle deposition velocity (Vd) values, currently under-parameterised in most modell
62 , and lateral nucleus of the area ventralis [Vd, Vv, Vc, and Vl, respectively]), as well as preoptic
64 (kloss); and the tracer distribution volume (Vd), which is an index of dopamine storage capacity.
68 CI, 0.434-0.827) for those receiving Kd56 vs Vd, respectively; median overall survival (OS) was 42.1
69 regional injuries: equation [see text] where Vd is the volume of lung irradiated to dose d, and Rd is
74 nalysis of the binding potential [Bmax/(Kd x Vd)] using the assumption of equal partition coefficient