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1                                              PPROM likely involves functional loss of sgp130.
2 al neutrophil infiltration that peaked after PPROM, whereas decidua from gestational age-matched cont
3 o a unit policy of no-use of tocolysis after PPROM, a liberal or restricted policy is not associated
4 whether a unit policy of tocolysis use after PPROM is associated with prolonged gestation and improve
5 nt association between the -656 T allele and PPROM (P < 0.002).
6 5) association between the -656 T allele and PPROM.
7 nd between fetal carriage of a 2G allele and PPROM.
8 s that follow spontaneous preterm labour and PPROM-together called spontaneous preterm births-are reg
9 ded 607 women with a singleton pregnancy and PPROM at 24-29 weeks' gestation, of whom 101, 195 and 31
10 ntify early pregnancy biomarkers of SPTB and PPROM from the maternal genome and transcriptome.
11 nscriptomic candidate biomarkers of SPTB and PPROM that require validation in diverse populations.
12 ant women who ultimately experience sPTL and PPROM.
13  and spontaneous preterm birth presenting as PPROM or preterm labor, and it suggests that bleeding is
14 l cells may explain how abruption-associated PPROM promotes decidual neutrophil infiltration.
15 extracellular matrix in abruption-associated PPROM, we examined whether decidual neutrophil infiltrat
16 nfiltration complicates abruption-associated PPROM.
17  membrane weakening and abruption-associated PPROM.
18 old increased risk of earlier preterm birth, PPROM, and preterm labor.
19 adverse pregnancy outcomes of preterm birth, PPROM, placental abruption, and pre-eclampsia aggregate
20  (2.6-5.5), 8.1 (7.5-8.8) for preterm birth, PPROM, placental abruption, and pre-eclampsia, respectiv
21 -5.3), and 4.5 (4.4-4.8), for preterm birth, PPROM, placental abruption, and pre-eclampsia, respectiv
22 0.0009) born from pregnancies complicated by PPROM compared with controls (odds ratio of 3.22, 95% co
23 estricted and liberal tocolysis policies for PPROM.
24 ased in IAI, whereas sgp130 was decreased in PPROM.
25 ecommend that women with expectantly managed PPROM remote from term receive antibiotics to reduce inf
26  that preterm premature rupture of membrane (PPROM) may be a confounding factor contributing to pheno
27 rm premature rupture of the fetal membranes (PPROM) to placental abruption.
28      Preterm premature rupture of membranes (PPROM) and thrombin generation by decidual cell-expresse
29 fter preterm premature rupture of membranes (PPROM), antibiotics and antenatal steroids are effective
30 rth, preterm premature rupture of membranes (PPROM), placental abruption, and pre-eclampsia.
31 , to preterm premature rupture of membranes (PPROM), the leading identifiable cause of preterm birth.
32 with preterm premature rupture of membranes (PPROM).
33 wing preterm premature rupture of membranes (PPROM).
34 ) or preterm premature rupture of membranes (PPROM; n = 91, 61 negative IAI and 30 positive IAI).
35  preterm premature rupture of the membranes (PPROM) (RR = 1.9, 95% CI: 1.1, 3.3).
36  preterm premature rupture of the membranes (PPROM) as well as preterm delivery (PTD).
37  preterm premature rupture of the membranes (PPROM), and (3) labour induction or caesarean delivery f
38  preterm premature rupture of the membranes (PPROM).
39  preterm premature rupture of the membranes (PPROM).
40 ured (preterm prelabor rupture of membranes [PPROM]) membranes.
41 this polymorphism contributes to the risk of PPROM.
42 ho ultimately underwent term birth, sPTL, or PPROM.
43 brane weakening, eliciting abruption-related PPROM and PTB.
44 Pregnancy outcomes were categorised as SPTB, PPROM (<= 34 weeks gestation, n = 53), high-risk term (H
45 ks, n = 126) or low-risk (no history of SPTB/PPROM) term (LTERM, >= 39 weeks, n = 188).
46 d PPARG1-FOXP3 gene set were associated with PPROM at week 20 of gestation and is related to inflamma
47 or alleles were individually associated with PPROM.
48 promoter activity in trophoblast cells, with PPROM with an odds ratio (OR) of 4.63 (P < 0.0001), wher
49 A total of 614 of 804 eligible gravidas with PPROM between 24 weeks' and 0 days' and 32 weeks' and 0
50 uption (decidual hemorrhage) with or without PPROM and in control placentas.