ライフサイエンスコーパス: multiple pregnancy

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1 apies to reduce the risk of preterm birth in multiple pregnancy.

2 ore than 1 embryo with its inherent risks of multiple pregnancy.

3 d, with 51 children (12%) known to be from a multiple pregnancy.

4 associated with the incidence of high-order multiple pregnancy.

5 d chance of achieving clinical pregnancy and multiple pregnancy.

6 benefit of revaccination over the course of multiple pregnancies.

7 d preterm delivery of artificially conceived multiple pregnancies.

8 ght less than 1000 g and 317 (20%) were from multiple pregnancies.

9 mor virus (MMTV)-infected females even after multiple pregnancies.

10 "best" embryos for transfer and to minimize multiple pregnancies.

11 ult in greater weight retention in mice with multiple pregnancies.

12 egenerated a differentiated gland even after multiple pregnancies.

13 rategy for increasing baby survival rates of multiple pregnancies.

14 ne stimulation with pituitary isografts; (3) multiple pregnancies; (4) DMBA alone; and (5) DMBA+pitui

15 Thus, multiple pregnancies and allostimuli appear to have prov

16 sk of non-Hodgkin's lymphoma associated with multiple pregnancies and an increased risk of non-Hodgki

17 included singletons (ie, not twins or other multiple pregnancies) and children for whom the mother w

18 regnancy or gestational diabetes, age <18 y, multiple pregnancy, and fetal anomaly.

19 Multiple pregnancy (aOR = 5.75; 95% CI 1.54-21.45) and i

20 igation of the relation of the occurrence of multiple pregnancy complications to CVD death over 5 dec

21 uded potential confounders and accounted for multiple pregnancies contributed by each man.

22 n the adult build alveolar structures during multiple pregnancies, demonstrating the existence of a W

23 years at cardiomyopathy diagnosis; 2.6% with multiple pregnancies) developed cardiomyopathy.

24 ipients with female donors who had undergone multiple pregnancies had a higher rate of chronic GVHD t

25 omary may reduce the incidence of high-order multiple pregnancy in infertile women, though only to a

26 . falciparum parasitemia during pregnancy on multiple pregnancy outcomes.

27 cantly with an increasing risk of high-order multiple pregnancy (P<0.001), as did younger age (P=0.00

28 easures analysis was used to account for the multiple pregnancies per woman.

29 1.16, 95% CI = 1.00-1.36, I(2) = 48.3%) and multiple pregnancy rates (OR = 1.50, 95% CI = 1.11-2.01,

30 ant results of clinical pregnancy as well as multiple pregnancy rates were observed among women who r

31 She had multiple pregnancy-related complications, including toxe

32 Multiple pregnancies should be monitored closely, and th

33 that long-term use of oral contraceptives or multiple pregnancies significantly increases the risk fo

34 rn weighing less than 1500 g--and those from multiple pregnancies than in infants of normal birthweig

35 After multiple pregnancies the p100 transgenics exhibited a du

36 Whether the number of high-order multiple pregnancies (those with three or more fetuses)

37 Graft survival in mothers with multiple pregnancies was poorer than those with a single

38 Among pregnancies, the rate of multiple pregnancy was 6.0% in the clomiphene group, 0%

39 The risk of high-order multiple pregnancy was significantly increased in women

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