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1 eclampsia, shoulder dystocia, and macrosomia in the treated group.
2 ures of efficacy also showed better outcomes in the treated group.
3 t decrease (P < .05) in vasomotor reactivity in the treated group.
4 educed fibrosis and greater vascular density in the treated group.
5 ; and TUNEL assay showed decreased apoptosis in the treated group.
6 21 of the 22 patients, and were less intense in the treated group.
7 -diastolic volume to body weight was reduced in the treated group.
8 perplasia, granuloma, or collagen deposition in the treated groups.
9 al evidence of protection from immune attack in the treated groups.
10 t in circulating antibody also were detected in the treated groups.
11 progression of left ventricular dysfunction in the "treated" group.
13 rly, the Shannon's alpha-diversity was lower in the treated group (10.60; 95% CI, 8.82-12.36) than th
15 BLFB were significantly increased (p<0.001) in the treated group (25.84+/-1.41%) compared with the c
18 rd fewer people on average reported headache in the treated groups (8.0%) than the placebo groups (12
21 cular resistance decreased by 21% (P < .001) in the treated group; a significant (22%) increase of th
24 infection were 0.018 episodes/patient-month in the treated group and 0.012 episodes/patient-month in
25 rejection were 0.031 episodes/patient-month in the treated group and 0.029 episodes/patient-month in
26 rejection were 0.070 episodes/patient-month in the treated group and 0.032 episodes/patient-month in
27 rejection were 0.044 episodes/patient-month in the treated group and 0.035 episodes/patient-month in
28 f isolated grade 2 rejection was 15.6 months in the treated group and 17.8 months in the nontreated g
31 and 10 years was 69% and 51 %, respectively, in the treated group and 67% and 41 %, respectively, in
32 ract surgery-related complications was 8.61% in the treated group and 8% in the control group (not si
33 8, 23, and 26, respectively, in the 3 babies in the treated group and at week 19 in the baby in the c
34 zed myasthenia developed in 8 of 76 patients in the treated group and in 15 of 82 patients in the non
35 control group were significantly attenuated in the treated group, as was thrombosis of renal glomeru
36 unotherapy, sIgE was significantly decreased in the treated groups compared to sham (P < 0.001), wher
38 tolic pressure (Ps), DevP, and (+dP/dt)/DevP in the treated groups compared with the control group.
39 gilance for threat information was decreased in the treated group, compared with the waiting group, t
40 efficient (ADC) measured by DW-MRI increased in the treated group consistent with cytotoxic edema.
41 Because the reduction of metastasis seen in the treated group could have resulted from 2-fold red
44 rbation rates were low, but there were fewer in the treated group (hazard ratio, 0.74; 95% confidence
46 ed by non-targets was significantly enhanced in the treated group, indicating memantine-associated im
47 f the gut microbiome was significantly lower in the treated group (inverse Simpson's alpha-diversity,
48 atients in the untreated group, the patients in the treated group mounted a 6-fold increased HIV-1 p2
55 in controls to 15.1+/-1.2 micromol/g dry wt in the treated group (P<0.01), and myeloperoxidase activ
56 mean+/-SEM) in controls to 118.1+/-8.2 mm Hg in the treated group (P<0.05), ATP increased from 11.0+/
57 ntrol groups compared with only 95 of 13,389 in the treated groups progressed from less severe to sev
58 t was not protective and increased morbidity in the treated group, suggesting that P-PMO may cause to
63 nge in CPT scores was -3.0 (range, -6 to +3) in the treated group versus +1.0 in the controls (range,
64 ment analysis indicated 0% of HBsAg+ infants in the treated group versus 2.84% in the NTx group (P=0.
65 (0 of 20 animals with CNS metastatic disease in the treated group versus 4 of 20 animals with CNS dis
66 transplanted patients, there were no deaths in the treated group versus 6 deaths in the control grou
67 asion (1 of 20 animals with invasive disease in the treated group versus 7 of 20 animals with invasiv
68 py, the resting regional cerebral blood flow in the treated group was significantly reduced, with a n
70 was administered at the time of reperfusion in the treated group, whereas saline was administered to
71 ibroblast growth factor proteins were higher in the treated group, whereas VEGF receptor 2 (Flk-1), a
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