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1  he showed wheals, loss of consciousness and low blood pressure.
2  restored urine concentration despite having low blood pressure.
3 nts who had longer periods of intraoperative low blood pressure.
4 , hypokalaemic alkalosis, hypercalciuria and low blood pressure.
5 usted hazard ratios were as follows: low CRP/low blood pressure, 1.0; high CRP/low blood pressure, 1.
6 s: low CRP/low blood pressure, 1.0; high CRP/low blood pressure, 1.87 (P=0.002); low CRP/high blood p
7 3) initial respiratory distress, (4) initial low blood pressure, (5) jaundice, (6) rupture of liver a
8                                         Very low blood pressure achieved on treatment was associated
9                    Infants and children with low blood pressure and adequate cardiac function after c
10                              Patients with a low blood pressure and moderate functional mitral regurg
11 reased vascular smooth muscle contractility, low blood pressure and thrombocytosis.
12     We hypothesised that different levels of low blood pressure are associated with benefit for some,
13              We investigated the presence of low blood pressure (BP) in 4,409 subjects referred for o
14        Studies have shown that both high and low blood pressure (BP) may play a role in the etiology
15                                              Low blood pressure by itself does not increase risk of p
16        Inherited hypokalaemic alkalosis with low blood pressure can be divided into two groups-Gitelm
17 , led to premature death, lack of white fat, low blood pressure, compensatory erythrocytosis, and hep
18 o promote infection, but the extent to which low blood pressure contributes remains unclear.
19           Therefore, the association between low blood pressure during pregnancy and poor perinatal o
20                                              Low blood pressure during pregnancy has been associated
21 atients, which includes resting tachycardia, low blood pressure, enlarged end-diastolic volume, high
22 ve slope difference in the short term in the low-blood-pressure group as compared with the standard-b
23 kidney volume was significantly lower in the low-blood-pressure group than in the standard-blood-pres
24 ventricular-mass index decreased more in the low-blood-pressure group than in the standard-blood-pres
25 and light-headedness were more common in the low-blood-pressure group than in the standard-blood-pres
26 k of incident depression, whereas those with low blood pressure had a higher risk of developing depre
27 e minor allele of this locus associates with low blood pressure in middle age, although the contribut
28 s previously been reported to associate with low blood pressure in middle age.
29             Previous studies have shown that low blood pressure is associated with increased mortalit
30 out mice lack both isozymes and they exhibit low blood pressure, kidney dysfunctions, and male infert
31 e by achieving a lifetime with very low LDL, low blood pressure, low glucose, normal body-mass index,
32 urprisingly, Rgs5(-/-) mice had persistently low blood pressure, lower in female mice than in male mi
33 by hypokalaemic alkalosis with salt-wasting, low blood pressure, normal magnesium and hyper- or normo
34                                          The low blood pressure of rats with CCl4-induced cirrhosis w
35 R = 1.667, 95% CI: 1.164-14.210, p = 0.006), low blood pressure (OR = 2.167, 95% CI: 2.104-13.150, p
36 p < 0.001), respiratory distress (p =0.007), low blood pressure (p = 0.024), jaundice (p = < 0.001),
37        A congenic strain introgressing the R low-blood-pressure QTL allele on chromosome 9 into the S
38 ains were constructed by introgressing Lewis low-blood-pressure QTL alleles for chromosomes 1, 5, 10,
39                           These animals have low blood pressure, renal vascular thickening, and a uri
40 tions of renal and extrarenal tissues to the low blood pressure seen in the AT(1A) receptor-deficient
41 ressure target (120/70 to 130/80 mm Hg) or a low blood-pressure target (95/60 to 110/75 mm Hg) and to
42 th parents and the first sibling were in the low blood pressure tertile (low-low group) and highest (
43            Since AT1A-deficient lpr mice had low blood pressure, these findings suggest that activati
44 , it is advisable to maintain a deliberately low blood pressure to facilitate clot formation and stab
45 er the authors controlled for these factors, low blood pressure was not associated with preterm birth
46                          However, women with low blood pressure were generally younger, shorter, ligh
47 e show that rats with biliary cirrhosis have low blood pressure, which is elevated by the CB1 recepto
48 , and control subjects were individuals with low blood pressure who had never taken antihypertensive

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