ライフサイエンスコーパス: multiple birth

1 dicator of higher embryo quality) on risk of multiple birth.

2 an intention-to-treat basis, accounting for multiple births.

3 comes that are known to be more prevalent in multiple births.

4 with an aim toward reducing the incidence of multiple births.

5 iated with a substantial rise in the rate of multiple births.

6 s of twin births and triplet or higher-order multiple births.

7 ears), non-European American, or products of multiple births.

8 increase in the risk of low birth weight in multiple births.

9 other's age, method of delivery, parity, and multiple births.

10 erved elevated NTD risk was mediated through multiple births.

11 Multiple births account for an increasing percentage of

12 rexia nervosa was independently predicted by multiple birth (adjusted hazard ratio = 1.33, 95% confid

13 We derived the rates of multiple births after natural conception from data on di

14 proposed as a strategy to reduce the risk of multiple birth and adverse pregnancy outcomes after in-v

15 tion, are associated with increased risks of multiple birth and concomitant sequelae and adverse outc

16 With the exception of monozygotic multiple birth and maternal hypertensive disorder, early

17 We identified an association between multiple births and early menopause, which connects even

18 antenatal corticosteroids, whether single or multiple birth, and birth weight.

19 uded cesarean-section delivery, birthweight, multiple birth, and infant survival status.

20 Gestational age at birth, birth order, multiple birth, and parental age were not associated wit

21 ncy diabetes mellitus, preterm preeclampsia, multiple birth, and termination of pregnancy.

22 Cesarean deliveries, multiple births, and births at less than 36 weeks' gesta

23 the youngest and oldest maternal age bands, multiple births, and deprivation (Index of Multiple Depr

24 t delivery, small for gestational age [SGA], multiple births, and male sex).

25 factors, in addition to GA at delivery, SGA, multiple births, and male sex.

26 s died, those with congenital abnormalities, multiple births, and mother and infant pairs who migrate

27 1.93), were primiparous (aOR = 2.03), had a multiple birth (aOR = 3.5), diabetes (aOR = 1.47), or ch

28 d their own estimate of the proportion of US multiple births attributable to non-ART ovulation stimul

29 clinical and economic burden associated with multiple births can be prevented through single-embryo t

30 crease in the age of asthma diagnosis across multiple birth cohorts.

31 lculations in consortia studies that include multiple birth cohorts.

32 lance data, they estimated proportions of US multiple births conceived naturally and by ART and assum

33 Almost 15% of inpatient costs for multiple births could have been avoided if ART twins and

34 as oral clefts, and individual patients with multiple birth defects (including clefts) have been show

35 ominant congenital disorder characterized by multiple birth defects including heart defects and myelo

36 s an autosomal dominant disorder that causes multiple birth defects including renal, ear, anal and li

37 Hug mutants exhibit multiple birth defects typical of ciliopathies, includin

38 ion or activation of Shh signalling leads to multiple birth defects, including holoprosencephaly, neu

39 The risk of perinatal death associated with multiple births did not explain this finding.

40 The unprecedented increase in multiple births during the past 3 decades is a major pub

41 h (2.7 [1.5-4.7]); the risks associated with multiple births explained some, but not all, of this exc

42 al number of 9873 live births were reported (multiple births from 1 pregnancy were counted as 1 live

43 Based on these data, the risk of multiple births from IVF varies by maternal age and numb

44 tments has led to an increase in the rate of multiple births in the United States.

45 Compared with singletons, multiple-birth infants consume significantly more hospit

46 odevelopmental impairment or mortality among multiple-birth infants of mothers with diabetes (aRR = 1

47 A total of 6925 multiple-birth infants were studied; 5775 of 6925 (83.4%

48 with the polycystic ovary syndrome, although multiple birth is a complication.

49 We compared rates of livebirth, multiple births, low birthweight (<2.5 kg), preterm birt

50 eable to one or two ancestral proteins: "the multiple birth model" for the evolution of protein seque

51 te 30.0/1,000) compared to 9,640 children of multiple births out of a total of 386,637 births in West

52 at diagnosis, birth weight, singleton versus multiple birth, parity, parental age, type of assisted c

53 the ART-NTD association was explained by the multiple-births pathway.

54 dds ratios and absolute risk differences for multiple birth, preterm birth, and low birthweight were

55 intensive use in 1981 and 1995 were having a multiple birth, primiparity, being married, and maternal

56 6 eyes developing SROP, BW, gestational age, multiple births, race, per capita income in the mother's

57 cycles, ICSI use was associated with a lower multiple birth rate compared with conventional IVF (30.9

58 Among women aged 35 to 39 years, the multiple-birth rate was 29.4% if 3 embryos were transfer

59 Among women 40 to 44 years of age, the multiple-birth rate was less than 25% even if 5 embryos

60 through 2011 were used to determine national multiple birth rates, and data on in vitro fertilization

61 Live-birth and multiple-birth rates (percentage of live births that wer

62 ART use worldwide and persistently high ART multiple-birth rates in several countries highlight the

63 Multiple-birth rates increased as high as 45.7% for wome

64 Live-birth and multiple-birth rates may vary by patient age and embryo

65 Multiple-birth rates varied by age and the number of emb

66 With 2 embryos transferred, multiple-birth rates were 22.7%, 19.7%, 11.6%, and 10.8%

67 Embryo quality was not related to multiple birth risk but was associated with increased li

68 plied a fetal survival factor, and used this multiple-birth risk estimate and their own estimate of t

69 transferring more than two embryos increased multiple-birth risk, with no corresponding increase in t

70 Greater maternal age did not decrease multiple-birth risk.

71 fer multiple embryos, but this increases the multiple-birth risk.

72 = 1.54; 95% CI: 0.95, 2.49), and monozygotic multiple birth (RR = 1.94; 95% CI: 1.26, 2.99).

73 re used to estimate the annual proportion of multiple births that were attributable to IVF and to non

74 Among multiple births, the prevalence of rectal and large inte

75 nal age is associated with decreased risk of multiple birth; using donor eggs from younger women may

76 Being part of a multiple birth was strongly associated with early menopa

77 Women having a multiple birth were much more likely to have had intensi

78 Rates of multiple birth were related to number of embryos transfe

79 Trends in multiple births were examined starting from 1998, the ye

80 Multiple birth, which is associated with adverse fetal,

81 ncreased occurrence of both miscarriages and multiple births, which has resulted in a great deal of c

82 sociation is mediated through the pathway of multiple births, while the ART-NTD association was expla

83 Since 1981, the percentage of women with multiple births who received intensive prenatal care (de