ライフサイエンスコーパス: low blood pressure

1 nts who had longer periods of intraoperative low blood pressure.

2 he showed wheals, loss of consciousness and low blood pressure.

3 restored urine concentration despite having low blood pressure.

4 , hypokalaemic alkalosis, hypercalciuria and low blood pressure.

5 epigastric fullness, following by fever and low blood pressure.

6 ut pain, fever, dyspnea, rapid heart rate or low blood pressure.

7 ersisting edema or escalating diuretics, and low blood pressure.

8 usted hazard ratios were as follows: low CRP/low blood pressure, 1.0; high CRP/low blood pressure, 1.

9 s: low CRP/low blood pressure, 1.0; high CRP/low blood pressure, 1.87 (P=0.002); low CRP/high blood p

10 3) initial respiratory distress, (4) initial low blood pressure, (5) jaundice, (6) rupture of liver a

11 Very low blood pressure achieved on treatment was associated

12 Infants and children with low blood pressure and adequate cardiac function after c

13 remained high during hospitalization in the low blood pressure and liberal oxygen target group but d

14 Patients allocated to a low blood pressure and liberal oxygen target had an incr

15 Patients with a low blood pressure and moderate functional mitral regurg

16 tin-4 receptor deficiency, that present with low blood pressure and normal glucose tolerance(4).

17 y, hypervigilance) which was associated with low blood pressure and startle reactivity.

18 reased vascular smooth muscle contractility, low blood pressure and thrombocytosis.

19 In response to low blood pressure and/or a decrease in extracellular fl

20 pregnant women include high blood pressure, low blood pressure, and high blood sugar levels.

21 We hypothesised that different levels of low blood pressure are associated with benefit for some,

22 Consequently, the derived LV and lifelong low blood pressure (BP) appear to be partly sustained by

23 We investigated the presence of low blood pressure (BP) in 4,409 subjects referred for o

24 Studies have shown that both high and low blood pressure (BP) may play a role in the etiology

25 Low blood pressure by itself does not increase risk of p

26 Inherited hypokalaemic alkalosis with low blood pressure can be divided into two groups-Gitelm

27 ctivity are also inherited causes of high or low blood pressure, clearly establishing its central rol

28 , led to premature death, lack of white fat, low blood pressure, compensatory erythrocytosis, and hep

29 o promote infection, but the extent to which low blood pressure contributes remains unclear.

30 at neither elevated intraocular pressure nor low blood pressure could account for the reduced blood f

31 Therefore, the association between low blood pressure during pregnancy and poor perinatal o

32 Low blood pressure during pregnancy has been associated

33 atients, which includes resting tachycardia, low blood pressure, enlarged end-diastolic volume, high

34 Hospitalizations and low blood pressure events did not differ significantly b

35 ve slope difference in the short term in the low-blood-pressure group as compared with the standard-b

36 ventricular-mass index decreased more in the low-blood-pressure group than in the standard-blood-pres

37 and light-headedness were more common in the low-blood-pressure group than in the standard-blood-pres

38 kidney volume was significantly lower in the low-blood-pressure group than in the standard-blood-pres

39 k of incident depression, whereas those with low blood pressure had a higher risk of developing depre

40 ctus arteriosus with ligation, dysautonomia, low blood pressure, hypotonic bladder requiring intermit

41 e minor allele of this locus associates with low blood pressure in middle age, although the contribut

42 s previously been reported to associate with low blood pressure in middle age.

43 essor norepinephrine is widely used to treat low blood pressure in sepsis but exacerbates immunosuppr

44 Previous studies have shown that low blood pressure is associated with increased mortalit

45 -function mutations lead to salt wasting and low blood pressure, it has been surmised that inhibitors

46 out mice lack both isozymes and they exhibit low blood pressure, kidney dysfunctions, and male infert

47 e by achieving a lifetime with very low LDL, low blood pressure, low glucose, normal body-mass index,

48 urprisingly, Rgs5(-/-) mice had persistently low blood pressure, lower in female mice than in male mi

49 by hypokalaemic alkalosis with salt-wasting, low blood pressure, normal magnesium and hyper- or normo

50 The low blood pressure of rats with CCl4-induced cirrhosis w

51 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

52 p < 0.001), respiratory distress (p =0.007), low blood pressure (p = 0.024), jaundice (p = < 0.001),

53 A congenic strain introgressing the R low-blood-pressure QTL allele on chromosome 9 into the S

54 ains were constructed by introgressing Lewis low-blood-pressure QTL alleles for chromosomes 1, 5, 10,

55 These animals have low blood pressure, renal vascular thickening, and a uri

56 tions of renal and extrarenal tissues to the low blood pressure seen in the AT(1A) receptor-deficient

57 Patients in the low blood pressure target group had lower mortality.

58 ressure target (120/70 to 130/80 mm Hg) or a low blood-pressure target (95/60 to 110/75 mm Hg) and to

59 ecent evidence suggested potential harm with low blood pressure targets in patients with peripheral a

60 th parents and the first sibling were in the low blood pressure tertile (low-low group) and highest (

61 Since AT1A-deficient lpr mice had low blood pressure, these findings suggest that activati

62 , it is advisable to maintain a deliberately low blood pressure to facilitate clot formation and stab

63 causal pathway that included fluid balance, low blood pressure, vasopressor use, hypokalemia, or hyp

64 er the authors controlled for these factors, low blood pressure was not associated with preterm birth

65 However, women with low blood pressure were generally younger, shorter, ligh

66 fluid overload or escalating diuretics, and low blood pressure were the individual criteria independ

67 e show that rats with biliary cirrhosis have low blood pressure, which is elevated by the CB1 recepto

68 , and control subjects were individuals with low blood pressure who had never taken antihypertensive