ライフサイエンスコーパス: perinatal mortality

1 increase in pregnancy loss (miscarriages and perinatal mortality).

2 wed up until 7 days after delivery to record perinatal mortality.

3 rm neurological morbidity, and 60% to 80% of perinatal mortality.

4 pid valve malformations associated with high perinatal mortality.

5 aspiration, retinopathy of prematurity, and perinatal mortality.

6 sease, particularly its role in maternal and perinatal mortality.

7 d malaria during pregnancy cause substantial perinatal mortality.

8 tational age, large for gestational age, and perinatal mortality.

9 rtality, while the other showed no change in perinatal mortality.

10 T1 knockout mice exhibited approximately 60% perinatal mortality.

11 gnancy may increase the risk of maternal and perinatal mortality.

12 ormal, neonates showed a higher frequency of perinatal mortality.

13 nces for the offspring in terms of increased perinatal mortality.

14 birth but have impaired growth and increased perinatal mortality.

15 dwarfism, sexual infantilism and significant perinatal mortality.

16 n the central nervous system associated with perinatal mortality.

17 ated with uterine rupture among 145 infants (perinatal mortality 124 per 1,000 total births, 95% CI 7

18 participants; OR, 0.19; 95% CI, 0.07-0.51), perinatal mortality (8 studies, 1140 participants; OR, 0

19 age and birthweight, containing all cases of perinatal mortality [8%]), and higher values of blood pr

20 They had high perinatal mortality, abnormal cranial dimensions, defect

21 on length (GL), calving difficulty (CD), and perinatal mortality, also known as stillbirth (SB), in c

22 ion of labour at >/=39 weeks and the risk of perinatal mortality among nulliparous women aged >/=35 y

23 TGFbeta2-null mice exhibit perinatal mortality and a wide range of developmental de

24 nduction of labour (IOL) around term reduces perinatal mortality and caesarean delivery rates when co

25 ies, albeit with no significant reduction in perinatal mortality and little evidence of neonatal bene

26 than in those that did not, but maternal and perinatal mortality and maternal morbidity did not diffe

27 ng pregnancy results in an increased risk of perinatal mortality and morbidity and is a significant f

28 Perinatal mortality and morbidity continue to be major g

29 ongenital heart defects are a major cause of perinatal mortality and morbidity, affecting >1% of all

30 es annually and is associated with increased perinatal mortality and morbidity, as well as poorer lon

31 We documented very low maternal and perinatal mortality and morbidity, confirming that the p

32 order that is a major cause for maternal and perinatal mortality and morbidity.

33 MARCKS-deficient mice exhibit universal perinatal mortality and numerous developmental abnormali

34 Perinatal mortality and severe neonatal morbidity did no

35 ndependent risk factor for preterm delivery, perinatal mortality, and other complications.

36 Slc23a1-/- dams exhibited approximately 45% perinatal mortality, and this was associated with lower

37 of these mice survived, but there was a high perinatal mortality, and those that survived had a decre

38 caesarean delivery was associated with lower perinatal mortality (AOR after planned caesarean at 39 w

39 Atox1(-/-) phenotype, resulting in increased perinatal mortality as well as severe growth retardation

40 osed prenatally or in infancy, and fetal and perinatal mortality associated with CHD in Europe.

41 We estimated the increased risk of perinatal mortality associated with jaundice during preg

42 National perinatal mortality audit programmes need to be implemen

43 between April 2009 and March 2014 to compare perinatal mortality between induction of labour at 39, 4

44 f adverse perinatal outcomes, which included perinatal mortality, bronchopulmonary dysplasia, sepsis,

45 ere was no significant effect on the odds of perinatal mortality but greater odds of neonatal unit ad

46 acenta) is associated with preterm birth and perinatal mortality, but associations with other neonata

47 The primary outcome was perinatal mortality, defined as fetal demise or death be

48 exhibit a unique phenotype characterized by perinatal mortality, disrupted cerebral cortical layerin

49 ondary endocrine problems and a high rate of perinatal mortality due to respiratory distress.

50 sociated with low birth weight and increased perinatal mortality, especially among primigravidae.

51 l inactivation of GATA-6 in VSMCs results in perinatal mortality from a spectrum of cardiovascular de

52 Newborn Lpcat1GT/GT mice showed varying perinatal mortality from respiratory failure, with affec

53 piratory dysfunction is a notorious cause of perinatal mortality in infants and sleep apnoea in adult

54 his report, we describe fetal hemorrhage and perinatal mortality in SLP-76-deficient mice.

55 as moderate to severe neonatal morbidity, or perinatal mortality in the absence of a major congenital

56 Perinatal mortality in these circumstances may therefore

57 e extent to which the effect of abruption on perinatal mortality is mediated through preterm delivery

58 Twin fetuses experience much higher rates of perinatal mortality/morbidity than age- and weight-match

59 lt in tissue damage, increasing the risk for perinatal mortality/morbidity.

60 Outcomes included mode of delivery, perinatal mortality, neonatal unit admission, postpartum

61 A was associated with a nonsignificant lower perinatal mortality of 14 per 1000 births in interventio

62 ) died before discharge, yielding an overall perinatal mortality of 45%.

63 of link protein could completely prevent the perinatal mortality of link protein-deficient mice and,

64 matopoiesis has been complicated by the high perinatal mortality of SIRT1-deficient mice (SIRT1(-/-))

65 Perinatal mortality of Slc23a1-/- pups born to Slc23a1-/

66 However, we also noted excessive perinatal mortality of T(-)GR(-) animals, caused by infe

67 sociation between smoke-free legislation and perinatal mortality, one showed significant reductions i

68 rrence of twin-to-twin transfusion syndrome, perinatal mortality, or severe neonatal morbidity.

69 data were analysed with regard to abortion, perinatal mortality, prematurity, toxaemia and congenita

70 Primary outcome measures were: perinatal mortality, preterm birth, and being small-for-

71 Our primary outcomes of interest were perinatal mortality, preterm birth, hospital attendance

72 f disease activity on spontaneous abortions, perinatal mortality, preterm delivery, and birth weight.

73 Three of 11 neonates died, giving a perinatal mortality rate of 27.3%.

74 %) had a fatal outcome, with a corresponding perinatal mortality rate of 9%.

75 Although perinatal mortality rates have improved for pregnant dia

76 obstetric complication associated with high perinatal mortality rates.

77 gene encoding c-Abl (AIM) display increased perinatal mortality, reduced fertility, foreshortened cr

78 stein anomaly and tricuspid valve dysplasia, perinatal mortality remained high.

79 TWH(-/-) mutant mice had increased perinatal mortality, retarded postnatal growth, and moto

80 and had gait ataxia, increased frequency of perinatal mortality, scoliosis, resting tremors and ptos

81 mission to a neonatal intensive care unit or perinatal mortality showed adverse trends, these changes

82 efects in the skin, lung, and intestine, and perinatal mortality that are reminiscent of EGF-R knocko

83 Perinatal mortality was 119 per 1,000 births with abrupt

84 ong women who were pregnant, miscarriage and perinatal mortality was 2.7 times higher (95% confidence

85 Perinatal mortality was higher with planned out-of-hospi

86 Perinatal mortality was nonsignificantly reduced after t

87 tion in SGA births, but not preterm birth or perinatal mortality, was observed in the Netherlands aft

88 ion to the neonatal intensive care unit, and perinatal mortality were similar among the infants whose

89 ity but did not report the overall effect on perinatal mortality, while the other showed no change in

90 barrier defects and fragile skin, leading to perinatal mortality with full penetrance.

91 preterm birth, which is the leading cause of perinatal mortality worldwide.