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1 had normal levels of fasting blood glucose, intravenous glucose tolerance, and HbA1c, and 15 of 16 s
2 asurements of fasting plasma glucose, HbA1c, intravenous glucose tolerance, and insulin secretory res
4 minimal model analyses of frequently sampled intravenous glucose tolerance (FSIGT) from the Insulin R
5 ous adipose biopsies, and frequently sampled intravenous glucose tolerance (FSIGT) testing were perfo
6 vity index (SI), disposition index (DI), and intravenous glucose tolerance (kg) were compared for eac
7 tion was assessed using a frequently sampled intravenous glucose tolerance test (first-phase insulin
8 aits were measured by the frequently sampled intravenous glucose tolerance test (four cohorts) or eug
9 ients were submitted to a frequently sampled intravenous glucose tolerance test (FSIGT) with the stim
10 rom the insulin-modified, frequently sampled intravenous glucose tolerance test (FSIGT), we estimated
13 ex (SI) calculated from a frequently sampled intravenous glucose tolerance test (FSIVGTT) after the m
14 lowing tests: 1) frequently sampled 0.3-g/kg intravenous glucose tolerance test (FSIVGTT) with MinMod
17 euglycemic hyperinsulinemic clamp (EHC), by intravenous glucose tolerance test (IVGTT) and by oral g
18 condition, we assessed glucose metabolism by intravenous glucose tolerance test (IVGTT) and euglycemi
20 exes with analogous indexes obtained from an intravenous glucose tolerance test (IVGTT) and hyperglyc
22 sing clamp and minimal model analysis of the intravenous glucose tolerance test (IVGTT) to document p
25 dministration of exogenous insulin during an intravenous glucose tolerance test allows the use of the
26 ivity index (S(i)) from a frequently sampled intravenous glucose tolerance test among African-America
27 nsitivity (S(i)) from the frequently sampled intravenous glucose tolerance test among African-America
28 easured directly from the frequently sampled intravenous glucose tolerance test among black, Hispanic
29 an oral glucose tolerance test (OGTT) and an intravenous glucose tolerance test and by a dual-energy
30 sulin secretion using the frequently sampled intravenous glucose tolerance test and insulin sensitivi
31 ects were examined with a frequently sampled intravenous glucose tolerance test and meal tolerance te
32 ulin sensitivity (determined by the modified intravenous glucose tolerance test and minimal model ana
33 were determined by the tolbutamide-modified intravenous glucose tolerance test and minimal modeling,
34 veness (S(G)), which were determined from an intravenous glucose tolerance test and minimal modeling.
35 ody insulin sensitivity index (S(I)) with an intravenous glucose tolerance test and minimal modeling.
37 second phase insulin release in response to intravenous glucose tolerance test and suppressed postpr
38 x ml(-1)), estimated by a frequently sampled intravenous glucose tolerance test and the minimal model
39 vity (SI), estimated by a frequently sampled intravenous glucose tolerance test and the minimal model
41 ixed meal and underwent a frequently sampled intravenous glucose tolerance test before and after 2 ye
45 point was change in SI by frequently sampled intravenous glucose tolerance test from entry to week 12
46 mal model analysis of the frequently sampled intravenous glucose tolerance test in 1,625 men and wome
47 ulin sensitivity (S(I)) was measured with an intravenous glucose tolerance test in obese HIV+ women r
48 tance was measured with a frequently sampled intravenous glucose tolerance test in the Insulin Resist
51 ulin action (Si), measured with the meal and intravenous glucose tolerance test models, was highly co
52 y and an insulin-modified frequently sampled intravenous glucose tolerance test on the second day.
55 l model analysis with the frequently sampled intravenous glucose tolerance test provides an effective
56 of EXN during mixed meal tolerance test and intravenous glucose tolerance test results in improved f
58 = 389) had first-phase insulin release on an intravenous glucose tolerance test that was higher than
63 lucose levels, urine glucose levels, and the intravenous glucose tolerance test were used to monitor
64 n sensitivity (SI) by the frequently sampled intravenous glucose tolerance test with analysis by the
65 th a validated, 12-sample, insulin-enhanced, intravenous glucose tolerance test with minimal model an
66 the tolbutamide-modified, frequently sampled intravenous glucose tolerance test with minimal modeling
67 mes were changes in Si (measured by using an intravenous glucose tolerance test) and cardiovascular r
68 changes of portal insulin (as measured by an intravenous glucose tolerance test) versus slow changes
69 rinsulinemic clamp), insulin secretion (25-g intravenous glucose tolerance test), and endogenous gluc
72 the curve and glucose disappearance rate on intravenous glucose tolerance test, all of which worsene
73 abolic testing by mixed meal tolerance test, intravenous glucose tolerance test, and arginine stimula
74 (S(I)) was measured by a frequently sampled intravenous glucose tolerance test, and CRP was measured
75 [AIR]), as derived from a frequently sampled intravenous glucose tolerance test, as well as common ca
78 index (SI) assessed by a frequently sampled intravenous glucose tolerance test, insulin secretion ra
79 ic clamp), acute insulin response (AIR, 25-g intravenous glucose tolerance test, n = 118 normal gluco
80 ive insulin) had higher DRs than first-phase intravenous glucose tolerance test-derived incremental i
107 phy, respectively; S(i) was assessed with an intravenous-glucose-tolerance test and minimal modeling.
108 were measured by using a frequently sampled intravenous-glucose-tolerance test and minimal modeling.
109 nemic-euglycemic glucose clamp technique and intravenous-glucose-tolerance test have indicated that i
110 tion were assessed with a frequently sampled intravenous-glucose-tolerance test, dual-energy X-ray ab
115 asured insulin sensitivity index (S(I)) from intravenous glucose tolerance testing among African-Amer
117 d first-phase insulin release in response to intravenous glucose tolerance testing, was observed afte
119 virtually identical to that obtained during intravenous glucose tolerance tests (71.6+/-6.1% of tota
120 lerance tests (OGTTs) and frequently sampled intravenous glucose tolerance tests (FSIGTs) were conduc
121 ch subject underwent four frequently sampled intravenous glucose tolerance tests (FSIGTT), one with t
123 and normalization of glucose disposal during intravenous glucose tolerance tests (IVGTT) remains crit
125 dlimb lymph insulin profile during simulated intravenous glucose tolerance tests (IVGTTs) in anesthet
128 Oral glucose tolerance tests (OGTTs) and intravenous glucose tolerance tests (IVGTTs) were perfor
130 l antibody-negative women underwent oral and intravenous glucose tolerance tests (OGTT; IVGTT), hyper
132 administration protocols, we performed three intravenous glucose tolerance tests in each of seven obe
134 cutaneous and intraperitoneal sensors during intravenous glucose tolerance tests in eight swine.
136 ed beta-cell function, we performed oral and intravenous glucose tolerance tests on mutation carriers
140 emic clamps in adults and frequently sampled intravenous glucose tolerance tests using Bergman minima
141 r sensor lag times (<4.2 min) in response to intravenous glucose tolerance tests versus burst NO-rele
142 ity (SI) as determined by frequently sampled intravenous glucose tolerance tests was measured over a
147 abetic, non-Amish subjects (n = 48), in whom intravenous glucose tolerance tests were performed, and
148 n levels returned to normal, and K values of intravenous glucose tolerance tests were significantly h
149 insulin secretion rates during both oral and intravenous glucose tolerance tests were used to generat
150 BCF) were determined from frequently sampled intravenous glucose tolerance tests, and total body fat
152 irst-phase insulin secretion, as measured by intravenous glucose tolerance tests, using up to 5,567 i
157 glycemic clamps), and insulin secretion [via intravenous-glucose-tolerance tests (IVGTTs)].Fifty-four
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