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1 ntitis was 0.97, whereas it was 1.04 for the healthy group.
2  positive in POTS groups and negative in the healthy group.
3 d Schaalia odontolytica were enriched in the Healthy group.
4 for the obesity group when compared with the healthy group.
5 o distinguish the probable AD group from the healthy group.
6  which made up 23% of the viral reads in the healthy group.
7 nsion over time, in the BD compared with the healthy group.
8 th corresponding thresholds derived from the healthy group.
9 ve results and belonged to the periodontally healthy group.
10 er in the bipolar disorder group than in the healthy group.
11  significantly more common in the previously healthy group.
12 dmann's area 10/11, which were absent in the healthy group.
13 % and 13% higher in the HD group than in the healthy group.
14 e asthmatic group; and PC20 decreased in the healthy group.
15 rtions of their Ztr spectra from that of the healthy group.
16 P from C. ochracea than in the periodontally healthy group.
17 and the FEV1/FVC ratio were derived from the healthy group.
18 periodontitis compared with the systemically healthy group.
19 roid group as compared with the systemically healthy group.
20 es were higher than respective values in the healthy group.
21 roid group as compared with the systemically healthy group.
22 ay, 7 days, and 6 weeks post-ablation in the healthy group.
23 database, was significantly increased in the healthy group.
24  of 73.7% in distinguishing healthy from non-healthy groups.
25 compared to controlled T2DM and systemically healthy groups.
26 ion than both psychotic bipolar disorder and healthy groups.
27 and biofluid parameters also in systemically healthy groups.
28 itis groups compared with both periodontally healthy groups.
29 ensory-evoked potentials between the FHD and healthy groups.
30 bacterial species in the diseased and in the healthy groups.
31 ategorized into unhealthy, intermediate, and healthy groups.
32 ar; P = 0.058) were faster than those of the healthy group (-0.11 mum/year), whereas the rate of vess
33 ar; P = 0.058) were faster than those of the healthy group (-0.11 um/year), whereas the rate of vesse
34 f eukaryotic viral reads were 0.063% for the healthy group, 0.131% for the acute-diarrhea group, and
35 nd diseased groups were analyzed separately (healthy group: [-0.23, correlation value] Student's t va
36 es with periodontitis (Group 4) and least in healthy (Group 1) and statistically significant between
37  individuals (n = 30 in each group), namely, healthy (Group 1), periodontitis (Group 2), diabetes (Gr
38 CT angiograms in 317 patients were reviewed (healthy group, 164; group with abnormalities, 153).
39 al parameters into three groups: group 1 (10 healthy), group 2 (10 well-controlled t2 DM among indivi
40 ese patients were divided into 3 groups: (a) healthy group: 30 patients, with <5% likelihood of CAD (
41 BALs from the future OB as compared with the healthy group (7.1 x 10(4) +/- 4.2 x 10(4) vs 3.4 x 10(4
42 BB was visualized, to greater degree, in the healthy group (90.2% vs 73.9% for group with abnormaliti
43 eater in the periodontitis group than in the healthy group (95% confidence interval, 6.5 to 19.2).
44 001), with the highest level observed in the healthy group and the lowest in the CP group.
45  studies as comparisons between diseased and healthy groups and not as comparisons between groups tha
46 gher in both patient groups, relative to the healthy group, and did not distinguish between the patie
47 (P = 0.07) and CP groups (P = 0.01) than the Healthy group, and similar to the CP and AgP groups (P >
48 e found in diseased groups compared with the healthy group at baseline.
49 n the vmPFC differed between the anxiety and healthy groups at relatively older ages.
50 oral cortex differed between the anxiety and healthy groups at relatively younger ages.
51 al prefrontal cortex and the striatum in the healthy group but not in the bipolar disorder group.
52 e anxious groups reported more fear than the healthy groups, but the anxious adolescent and adult gro
53 groups were higher than in the periodontally healthy groups, but the difference between the CP and DM
54 e significantly different between cancer and healthy groups by the Mann-Whitney U test.
55 ed the reward system in the chronic itch and healthy groups, confirming that this reward system has a
56 phils in severe COVID-19 cases compared to a healthy group, consistent with our observations in the m
57 cally achieved for all subjects from the two healthy groups except one (19/20, success rate = 95.0%).
58                  The ICC in the glaucoma and healthy groups for pRNFL (0.99 vs. 0.98), BMO (0.95 vs.
59 pared with the average number of RGCs in the healthy group, glaucomatous eyes had an average RGC loss
60             Subjects were categorized into a Healthy group (H, n = 20) and periodontitis/gingivitis g
61                                          The healthy group had Blood Lead concentrations (BLC), < 10
62               Most women (66.8%) were in the healthy group (HG); 17.1% were in the psychologically st
63 he decision-making task in both the ADHD and healthy groups; however, activation in the ADHD group wa
64 ngivitis (group G/n = 20), and periodontally healthy (group HP/n = 20) were recruited for this resear
65 ed into three groups, Group I: Periodontally healthy, Group II: Non-smokers with Stage III periodonti
66 was found between the hypertensive group and healthy group in demographic and clinical characteristic
67 ere found in CP groups than in periodontally healthy groups, in DM-CP than in CP, and in DM-CTRL than
68 l damage to the VMF (N = 12) compared with a healthy group matched for age and education (N = 24) and
69 eater predictor of virome alpha diversity in healthy groups (mean r(2)=0.380; 95% CI 0.597-0.163) tha
70 0) was significantly higher than that in the healthy group (n = 150) (p = 0.032), suggesting that the
71 ated with PLV after lung injury; and the PLV-healthy group (n = 6) was supported with PLV without lun
72  ~25% lower in healthy group O compared with healthy group non-O individuals.
73 ic risk, plasma VWF levels are ~25% lower in healthy group O compared with healthy group non-O indivi
74 ously diagnosed and treated glaucoma and one healthy group of 50 subjects.
75  and discrimination power between the AE and healthy group of 73.5%.
76 al variability, both in dCA and sCA, in this healthy group of elderly, in a range from low to high CA
77  by time after infection and to compare to a healthy group of the same age without previous virus inf
78                           In this relatively healthy group of volunteers, consumption of 1 cup fortif
79  and lung microbiomes differed in clinically healthy groups of HIV-infected and HIV-uninfected subjec
80 eriodontitis with moderate periodontitis and healthy group: oral hypoglycemic agents (17.4% versus 16
81 cantly higher compared with the systemically healthy group (p < 0.001).
82 metropic amblyopia (bilateral amblyopia) and healthy group (p < 0.001).
83 Related Protein 5 levels were highest in the healthy group (p < 0.001).
84 ning group was significantly higher than the healthy group (P < 0.05).
85 her GCF Bcl-xl levels than the periodontally healthy group (p < 0.05).
86 her clinical periodontal parameters than the healthy group (p < 0.05).
87 tis group were significantly higher than the healthy group (P < 0.05).
88 n FD values were significantly higher in the healthy group (P < 0.05).
89 p were significantly lower than those in the healthy group (P < 0.05).
90 (2.8 times) in the gingivitis group than the healthy group (P </=0.02).
91 ns remained significantly higher than in the healthy group (P </=0.04).
92 nd serum IL-6 concentrations than the PCOS + healthy group (P <0.0001).
93 roups had higher IL-6 total amounts than the healthy group (P <0.008).
94 gnificantly higher in the AgP group than the Healthy group (P = 0.01), and similar between Healthy an
95  the PCOS + gingivitis group than the PCOS + healthy group (P = 0.030).
96  higher in diabetic groups than systemically healthy groups (P < 0.001) and in H-P compared to H-H (P
97 s compared with gingivitis and periodontally healthy groups (p < 0.05).
98 levels than the gingivitis and periodontally healthy groups (p < 0.05).
99  TNF-alpha total amounts than gingivitis and healthy groups (P < 0.05).
100 oup were significantly higher than G-AgP and healthy groups (P < 0.05).
101 groups compared with both the gingivitis and healthy groups (P <0.008).
102 stational diabetes mellitus vs. 37.3% in the healthy group; p=0.38).
103                             Finally, for the healthy group, physostigmine decreased stimulus and task
104  1.99, and 2.28 (severe periodontitis versus healthy group), respectively.
105  (p < 0.01 or p < 0.001) as comparing to the healthy group, respectively.
106 ficantly enriched in the diseased and in the healthy groups, respectively.
107  the ABPA and CCPA groups, compared with the healthy group, suggesting that differences in PPBP level
108 ion of IL-35 was significantly higher in the healthy group than the other groups (P = 0.002).
109 ase-8 was significantly higher in the CP and Healthy groups than the AgP group (P = 0.00), and simila
110 ignificantly higher incidence of PI than the healthy group that demonstrated PIM.
111 y numbers was found between the diseased and healthy group, the similar detection rate in both groups
112                               In the OCD and healthy groups, the mean (SD) ages were 27.4 (7.1) years
113 ferent between cancer, positive control, and healthy groups using the Kruskal-Wallis test.
114               The threshold derived from the healthy group was close to the histopathology-derived th
115 value was statistically significant when the healthy group was compared with the CP and MI groups but
116 with type 1 diabetes mellitus (T1DM) and the healthy group, we aimed to understand the possible chang
117                           In contrast to the healthy group, we found that the probable AD patients ha
118 cant difference in the use of n-grams as the healthy group were able to identify and make sense of mo
119 /mL and serum = 0.05 ng/mL) in periodontally healthy group were considerably lower than that in the p
120 criminatory power between the pathologic and healthy groups were <10(-3) for data on Takotsubo syndro
121 viduals with no raised acute-phase proteins (healthy group) were much the same as those obtained by a
122 tched individuals with healthy periodontium (healthy group) were selected.
123 ed >30%, the upper 95% bounds of a reference healthy group without known cardiac disease (n = 28).
124                        Two control groups, a healthy group without respiratory symptoms and a symptom

 
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