ライフサイエンスコーパス: second trimester

1 100 healthy pregnant women, starting in the second trimester.

2 with moderate methyl bromide use during the second trimester.

3 ing outside of the guideline as early as the second trimester.

4 with adjustment for energy costs during the second trimester.

5 le the ventricle size decreases in the later second trimester.

6 with periodontitis when assessed during the second trimester.

7 surface remains smooth until the end of the second trimester.

8 erebral wall throughout the remainder of the second trimester.

9 e thrombocytopenia with bleeding only in the second trimester.

10 ase with maternal fever, particularly in the second trimester.

11 es of pregnancies with CHDs diagnosed in the second trimester.

12 2 units, P < 0.03) trimesters but not in the second trimester.

13 nner) and snacks consumed per day during the second trimester.

14 old with supplement use during the first and second trimester.

15 pproximately twofold when use dated from the second trimester.

16 e configuration was most common early in the second trimester.

17 reduction when supplement use started in the second trimester.

18 onates born to mothers vaccinated during the second trimester.

19 he development of the fetal brain during the second trimester.

20 sembles the small bowel until the end of the second trimester.

21 second trimester and long bones later in the second trimester.

22 lular density declined from the first to the second trimester.

23 ollutant concentrations during the first and second trimester.

24 ked the presence of the CD44(+) cells in the second trimester.

25 tussis in infant than vaccination during the second trimester.

26 vation in tissue resident neutrophils in the second trimester.

27 ostpartum, but fetal loss was highest in the second trimester.

28 questionnaire administered in the first and second trimesters.

29 scores between the 2 groups at the first and second trimesters.

30 Mean second trimester (15-22 weeks' gestation) serum sTNFp55

31 yses showed that, compared with mothers with second-trimester 25(OH)D concentrations in the highest q

32 Fetal viability was low in the second trimester (29.2%) and much higher (95.3%) in the

33 ) and third (53%) trimesters than during the second trimester (33%).

34 ted with fetal demise was more common in the second trimester (55.3%), and preterm labor (52.3%) and

35 at least one study ultrasound in 5.1% by the second trimester, 7.9% by the third trimester, and 10.2%

36 ter, 9.7 g lower when it occurred during the second trimester (95% CI: -14.5, -4.8), and 3.3 g lower

37 Rats infected in the early second trimester after implantation (gd 11) did not expe

38 PCR testing of second-trimester amniotic fluid for U. urealyticum can i

39 birth rates and rates of abortion during the second trimester among a subgroup of minors who were 17.

40 rate of weight gain was 306 g/wk during the second trimester and 247 g/wk during the third trimester

41 partum, and their diets were assessed in the second trimester and at 3 and 12 months postpartum (n =

42 lled and were screened in the program by the second trimester and had at least 3 additional prenatal

43 lled and were screened in the program by the second trimester and had at least 3 additional prenatal

44 driven by an association with AC earlier in second trimester and long bones later in the second trim

45 r) of trihalomethanes experienced during the second trimester and pregnancy overall may affect fetal

46 ation between maternal IL-8 level during the second trimester and risk of schizophrenia spectrum diso

47 eptible to infection with RhCMV early in the second trimester and that intrauterine infection results

48 he first trimester with 26.1 to 36.1% in the second trimester and to 51.2% in the third trimester of

49 for subjects with exposure to famine in the second trimester and was increased significantly for sub

50 dence interval [CI], -32 to -1 g) during the second trimester and weighed 74 g less (95% CI, -140 to

51 egnancy, 18 in the first trimester, 4 in the second trimester, and 1 in the third trimester.

52 ted in the first trimester, 8 (33.3%) in the second trimester, and 2 (8.3%) in the third trimester.

53 first trimester, 52% after infection in the second trimester, and 29% after infection in the third t

54 part of the first trimester, 8.5E-03 in the second trimester, and 5.1E-03 in the third trimester.

55 s increased substantially from early to late second trimester, and a shift was observed from 1-->4/1-

56 in the first trimester, by 350 kcal/d in the second trimester, and by 500 kcal/d in the third trimest

57 ed intraperitoneally with RhCMV early in the second trimester, and pregnancies were terminated by hys

58 diverge and become nonoverlapping during the second trimester, and the generation of the intestinal g

59 ns for three-months preconception, first and second trimester, and whole-pregnancy averages.

60 microGy, first trimester; 7.9-76.7 microGy, second trimester; and 51.3-130.8 microGy, third trimeste

61 facial dysmorphism, which was diagnosed on a second-trimester antenatal real-time three-dimensional u

62 in concentrations >120 g/L at the end of the second trimester are associated with a </=3-fold increas

63 n levels in mantle dentine formed during the second trimester (as (55)Mn:(43)Ca area under curve) wer

64 f the first scan, which was confirmed during second-trimester assessment.

65 rolled at prenatal care clinics during their second trimester, at which time blood, stool, urine, and

66 ne (SVZ) expanded massively during the early second trimester, becoming densely populated with neural

67 ared with fetuses diagnosed with CHDs in the second trimester between 2007 and 2013.

68 abolism were measured from random nonfasting second-trimester blood samples.

69 h women who entered care during the first or second trimester but did not use prenatal supplements, s

70 lities, is most often identified in the late second trimester, carries a substantial mortality in the

71 The second trimester cells also engrafted secondary recipien

72 exposures (OR = 2.0; 95% CI: 1.1, 3.6), and second-trimester chlorpyrifos applications (OR = 3.3; 95

73 and child's age and sex, the top quartile of second-trimester choline intake was associated with a ch

74 me exercise (> or = 60 days in the first and second trimesters combined) had a protective effect on p

75 rotective against low weight gain during the second trimester compared with multivitamins alone.

76 were apparent early in pregnancy, during the second trimester: compared with uninfected women, women

77 placenta, yet little is known regarding the second-trimester decidual environment.

78 Yet, administration of alpha-GalCer in the second trimester did not cause pregnancy loss.

79 Second-trimester diet was assessed by food frequency que

80 We assessed first- and second-trimester diet with the use of food-frequency que

81 To characterize the differences between second trimester Down syndrome (DS) and euploid fetuses,

82 The second-trimester effect remained when we estimated popul

83 This second-trimester effect seems somewhat stronger in men (

84 Women's second trimester EPDS scores negatively correlated with

85 -based vitamin D intake during the first and second trimesters (equivalent to the amount of vitamin D

86 lbirth risk, and preconception and first and second trimester exposures were not.

87 tation < 37 weeks) births for the first- and second-trimester exposures in a logistic mixed model, an

88 imaging presentation of CPAM type II in the second trimester, extensively involving all lobes of the

89 ssion was significantly reduced in first and second trimester fetal cerebral cortex compared with adu

90 site structures than those seen in first and second trimester fetal tissues.

91 with childhood kidney volume, whereas higher second trimester fetal weight was positively associated

92 cant effect on ZNF804A allelic expression in second-trimester fetal brain, with the schizophrenia ris

93 ells are the predominant blood subset in the second-trimester fetus, whereas Vdelta1(+) and Vdelta3(+

94 Our analyses of second trimester fetuses exposed at the time of meiotic

95 Second-trimester fetuses diagnosed with a CHD between 20

96 Second-trimester fetuses with trisomy 21 have a signific

97 hird-trimester fetuses and in 16 (46%) of 35 second-trimester fetuses.

98 Maternal exposure to second-trimester fever was associated with increased ASD

99 Studies were included if they recorded second-trimester findings of ultrasonographic markers, c

100 the authors studied associations of maternal second-trimester fish intake and erythrocyte mercury lev

101 nd showed highest levels at the start of the second trimester followed by a gradual decline through t

102 III (532 fetuses diagnosed with a CHD in the second trimester from 1996 to 2001, the period before fi

103 med on gestational day (GD) 65 (n = 8; early second trimester), GD 110 (n = 4; early third trimester)

104 The spectrum of CHDs seen in the second-trimester groups differed after first-trimester s

105 inferiority study comparing the influence of second-trimester (GW 13-25) vs third-trimester (>/=GW 26

106 were screened in the MIHP by the end of the second trimester had lower odds of VLBW (odds ratio [OR]

107 uman semilunar valve leaflets from first and second trimester hearts.

108 -immunopanned oligodendrocytes isolated from second trimester human fetal spinal cord.

109 nvestigate the development of these cells in second trimester human fetal tissues.

110 Functional in vitro assays showed that second-trimester human decidua conditioned medium stimul

111 -to-noise-ratio DTI data of fixed tissues of second-trimester human fetal brains were acquired and an

112 vivo transplantation model by transplanting second-trimester human fetal heart tissues s.c. into the

113 y initiated molecular cytogenetic studies of second-trimester human fetal ovaries, allowing us to dir

114 ch the brain is developmentally similar to a second-trimester human fetus.

115 Already in second-trimester human skin, the phenotype of blood and

116 The second-trimester IL-8 levels in mothers of offspring wit

117 wing i.v. rhCMV inoculation during the early second trimester in two of three rhCMV-seronegative preg

118 spectrum of CHDs diagnosed in the first and second trimesters in the same time period differed signi

119 In the second trimester, inadequate GWG was predicted with a se

120 exposure (> or = 70 microg/liter) during the second trimester increased the risk of term low birth we

121 In the second trimester, increased O(2) tension promotes protea

122 Mean second-trimester intakes were 328 (standard deviation (S

123 ry adverse consequences of DS evident in the second trimester, leading to testable hypotheses about p

124 g toward the tip along the fibrosal layer in second trimester leaflets.

125 High-activity lupus in the first and second trimesters led to a 3-fold increase in pregnancy

126 goal of this study was to determine whether second-trimester levels of four cytokines-interleukin-8

127 ifications to assess the association between second-trimester levels of maternal serum alpha-fetoprot

128 ry in a previous pregnancy of preterm birth, second trimester loss, preterm premature fetal membrane

129 nd early pregnancy outcomes in the first and second trimester (<24 weeks of gestation)?

130 such as the Integrated test using first and second trimester markers.

131 There is a direct association between second-trimester maternal serum alpha-fetoprotein levels

132 ernal age alone, 60-70% for maternal age and second-trimester maternal serum biochemical testing, 75%

133 k group by a combination of maternal age and second-trimester maternal serum biochemistry gives a det

134 schizoaffective disorder) who had available second-trimester maternal serum samples.

135 Early second-trimester maternal Tdap immunization significantl

136 A thickened nuchal fold in the second trimester may be useful in distinguishing unaffec

137 t obstruction, early intervention during the second trimester may prevent the development of ventricu

138 Second trimester median PlGF was 31% lower at 14 weeks (

139 revious pregnancy also was terminated in the second trimester medically due to the ultrasound diagnos

140 ate first trimester MIA (n = 6), and 2) late second trimester MIA (n = 7).

141 sh whether antibiotic treatment early in the second trimester might reduce these risks in a general o

142 ere not associated with an increased risk of second-trimester miscarriage.

143 d with a significant increase in the risk of second trimester miscarriages.

144 could also be detected at high frequency in second-trimester mucosal tissues (e.g., the intestine an

145 ere obtained in early pregnancy (n = 1), the second trimester (n = 2), and the third trimester (n = 3

146 lammation (IAI), we studied 301 women during second trimester (n = 39), third trimester (n = 40), and

147 adder, and amniotic fluid of miniature pigs (second trimester, n = 2; third trimester, n = 2).

148 ward flow velocity increased, peaking in the second trimester (nonsignificant), but returned to basel

149 = 1.12, 95% confidence interval: 0.79, 1.59; second trimester odds ratio = 1.30, 95% confidence inter

150 the lateral ganglionic eminence late in the second trimester of development (23-24 weeks postconcept

151 ve decrease in ZNF804A expression during the second trimester of fetal brain development.

152 posed to the influenza epidemic during their second trimester of fetal development compared with cont

153 l and paternal psychological distress at the second trimester of gestation and 3 years after delivery

154 ventricular zone of human fetal brain at the second trimester of gestation and to study their progeny

155 stress) was obtained by questionnaire in the second trimester of gestation by using the Brief Symptom

156 fferentially to cortical neurogenesis at the second trimester of gestation in human cerebral cortex.

157 zations in the human fetal cortex during the second trimester of gestation.

158 and in human brain tissue from the first and second trimester of gestation.

159 abundant in the airway epithelium during the second trimester of human development than after birth.

160 During the second trimester of human fetal development, neural stru

161 associated with myelin formation during the second trimester of human gestation.

162 th higher maternal glucose levels during the second trimester of pregnancy (2-h glucose after the ora

163 that syncytiotrophoblasts isolated from the second trimester of pregnancy also constitutively releas

164 Serum samples were collected during the second trimester of pregnancy and analyzed for levels of

165 t count of greater than 150 x 10(9)/L by the second trimester of pregnancy and only 2% of term infant

166 d fulminant hepatic failure (FHF) during the second trimester of pregnancy and underwent a successful

167 atio of omega-6-to-omega-3 PUFAs in the late-second trimester of pregnancy are associated with less w

168 Women given albendazole in the second trimester of pregnancy had a lower rate of severe

169 serum level of alpha-fetoprotein during the second trimester of pregnancy is a marker of placental d

170 amined the effects of cocaine use during the second trimester of pregnancy on cerebral neocortical vo

171 ) or matched placebo (n=1205) daily from the second trimester of pregnancy until delivery.

172 ids, especially 16:1t and 18:2tc, during the second trimester of pregnancy was associated with greate

173 pecific maternal serum IgG levels during the second trimester of pregnancy were evaluated in relation

174 echocardiography is usually done during the second trimester of pregnancy, but waiting until that ti

175 trophoblast cell line (HTR8), from first and second trimester of pregnancy, express receptors relevan

176 orionic gonadotropin was measured during the second trimester of pregnancy, seeking information about

177 cy cohort using a 3-d food record during the second trimester of pregnancy.

178 ted food frequency questionnaires during the second trimester of pregnancy.

179 experienced intrauterine fetal demise in the second trimester of pregnancy.

180 syndrome is now routinely offered during the second trimester of pregnancy.

181 ies visualized on ultrasound scan during the second trimester of pregnancy.

182 ous group of 448 women was followed from the second trimester of their first pregnancy.

183 ealing occurs in fetal skin in the first and second trimesters of development.

184 12, betaine, and folate during the first and second trimesters of pregnancy and offspring visual memo

185 ures of maternal intake during the first and second trimesters of pregnancy and serum 25-hydroxyvitam

186 /mineral supplement use during the first and second trimesters of pregnancy by low income, urban wome

187 de screening and treatment) in the first and second trimesters of pregnancy compared to the third tri

188 tritional deficiency during the first and/or second trimesters of pregnancy exhibited increased risk

189 rentiation and invasion during the first and second trimesters of pregnancy were associated with down

190 uency questionnaire in each of the first and second trimesters of pregnancy.

191 ternal uterine arteries during the first and second trimesters of pregnancy.

192 ed with dichorionic twin fetal growth in the second trimester only, driven by an association with AC

193 In contrast, bleeding in the second trimester only, of a single episode, on a single

194 g/m(3) increase in PM2.5 exposure during the second trimester only, which remained unchanged after ad

195 Recommending immunization from the second trimester onward would widen the immunization opp

196 recommend a monthly dose of IPTp-SP from the second trimester onwards.

197 (first trimester OR, 5.1; 95% CI, 1.9-13.2; second trimester OR, 0.5; 95% CI, 0.2-1.2; and third tri

198 t trimester (OR = 1.93; 95% CI: 1.55, 2.40), second trimester (OR = 1.67; 95% CI: 1.35, 2.08), third

199 olumns, and syncytiotrophoblast of first and second-trimester placenta as well as syncytiotrophoblast

200 First and second trimester placental tissues from normal pregnanci

201 ibit a lobular pattern of enhancement, while second-trimester placentas exhibit heterogeneous enhance

202 Second trimester PlGF measurements are of limited value.

203 We used residential addresses to estimate second-trimester PM2.5 and black carbon exposure via a c

204 ght, P < 0.0007, and 1-kg weight gain in the second trimester predicted a 26-g increase in newborn we

205 nders, maternal weight gain in the first and second trimesters predicted newborn weight (1-kg weight

206 other hand, preterm cervical ripening in the second trimester predicts preterm birth.

207 s and heterogeneous placental enhancement in second-trimester pregnancies.

208 umbilical cord serum collected from elective second trimester pregnancy terminations.

209 ratio, 4.68; 95% CI, 3.74 to 5.86); loss of second-trimester pregnancy, 16.4% vs. 1.7% (hazard ratio

210 PBDEs and their metabolites (OH-PBDEs) among second trimester pregnant women recruited from San Franc

211 een intra-amniotic U. urealyticum in healthy second-trimester pregnant women and subsequent pregnancy

212 Second-trimester prenatal ultrasound is widely used in a

213 y low-dose aspirin beginning as early as the second trimester prevented clinically important health o

214 1-SD (0.36 g . kg(-1) . d(-1)) increment in second-trimester protein intake corresponded to a -0.10

215 Mean (range) second-trimester protein intake was 1.4 g . kg(-1) . d(-

216 ys through 13 weeks 6 days of gestation) and second-trimester quadruple screening (measurement of alp

217 ning at 11 weeks of gestation is better than second-trimester quadruple screening but at 13 weeks has

218 at 11, 12, and 13 weeks, respectively; with second-trimester quadruple screening, 81 percent; with s

219 ening but at 13 weeks has results similar to second-trimester quadruple screening.

220 cohort, we examined associations of maternal second trimester red blood cell mercury (RBC-Hg) concent

221 R) for 1 mug/L=1.05; 95% CI: 1.00, 1.11] and second trimesters (RR for 1 mug/L=1.03; 95% CI: 1.00, 1.

222 gnancies; two LB (no malformations), and one second trimester SA.

223 in isolation or with bacteria in first- and second-trimester samples.

224 ial was conducted to evaluate the effects of second-trimester scaling and root planing and the use of

225 etuses with this abnormality can have normal second-trimester scans and develop abnormal US findings

226 We did second-trimester scans and neonatal follow-up for the wo

227 tuses we diagnosed small muscular VSD on the second-trimester scans.

228 Second trimester screening for Down's syndrome is widely

229 adruple test should be the test of choice in second trimester screening for Down's syndrome.

230 iocentesis, or 3 times greater if they had a second trimester screening test (Quadruple test) and tre

231 itive rate) and is more effective than other second trimester screening tests.

232 mester (Group I, 127 fetuses) or only in the second-trimester screening (Group II, 344 fetuses), were

233 erform first-trimester screening, to perform second-trimester screening, or to use strategies incorpo

234 rations of 10 BFRs were measured in maternal second trimester serum samples stored from routine scree

235 Maternal second-trimester serum levels of IL-8, IL-1beta, IL-6, a

236 PCB congeners and 2 OCPs measured in banked second-trimester serum samples were compared between the

237 vaginosis with oral clindamycin early in the second trimester significantly reduces the rate of late

238 Second-trimester spatiotemporal exposures ranged from 8.

239 On the basis of second-trimester-specific guidelines, inadequate GWG can

240 A second-trimester stillbirth occurred during the course o

241 rofiles of progenitors between the first and second trimesters suggest that these cells had gestation

242 bacteria were detected more often during the second trimester than during the first--Ureaplasma ureal

243 In the second trimester, the estimated mean (+/-SD) total trans

244 osed to fluoxetine only during the first and second trimesters, the 73 infants exposed during the thi

245 sease and acute leukemia diagnosed after the second trimester, therapeutic termination of the pregnan

246 )) increase in PM2.5 in the first trimester, second trimester, third trimester, and whole pregnancy w

247 high supplemental folic acid intakes in the second trimester, those with the lowest tertile of vitam

248 eived saline injections at the same first or second trimester time points or were untreated.

249 y Doppler ultrasound is commonly used in the second trimester to identify pregnancies destined to dev

250 mester fetal sheep previously exposed in the second trimester to maternal alcohol "binges" (1.5 g/kg

251 diagnoses in a population exposed during the second trimester to the 1957 influenza epidemic.

252 of uterine artery resistance index from the second trimester to the third were associated with the r

253 nd lifestyle characteristics, track from the second trimester to the third, and are associated with t

254 haracteristics and track moderately from the second trimester to the third.

255 From 7400 second-trimester ultrasound referrals, 145 patients were

256 r dust samples and mother's blood during the second trimester; umbilical cord blood at birth; and she

257 5% increase in odds of preterm birth, while second-trimester unemployment was associated with a 3% d

258 en antibodies were present from early in the second trimester until term.

259 sed in utero arsenic exposure using maternal second-trimester urinary arsenic, maternal prepregnancy

260 Standard second-trimester US before 22 weeks of gestation may not

261 ds ratio=0.77, 95% CI=0.43-1.36), first- and second-trimester use (odds ratio=0.84, 95% CI=0.40-1.77)

262 ds ratio=0.56, 95% CI=0.25-1.24), first- and second-trimester use (odds ratio=0.90, 95% CI=0.37-2.17)

263 ated risk increase for Caucasians during the second trimester was 37% (95% CI: 0.80, 2.36), while for

264 Dietary intake during the second trimester was assessed with a food-frequency ques

265 nts, supplement use starting in the first or second trimester was associated with approximately a two

266 l proximity to methyl bromide use during the second trimester was associated with markers of restrict

267 ing untreated genital herpes during first or second trimester was associated with more than double th

268 Higher maternal wheat intake during the second trimester was associated with reduced atopic derm

269 the index group who were exposed during the second trimester was due to a significant (P < .002) ele

270 no use) within 5 km of the home during the second trimester was negatively associated with birth we

271 NO2 in the second trimester was negatively associated with spontane

272 rsenic measured in maternal urine during the second trimester was not associated with methylation in

273 otal trans fatty acid consumption during the second trimester was positively associated with the feta

274 l weight gain from 14 to 20 and 21 to 27 wk (second trimester) was significantly associated with incr

275 tionnaires administered during the first and second trimesters, we assessed maternal intake of common

276 the women who contracted ZVD in the first or second trimester were still pregnant at the time of this

277 ations between GWG beginning as early as the second trimester with fetal cord blood leptin and strong

278 concentrations were lowest in the first and second trimesters with levels comparable to those observ

279 nd 2 with PET/CT), 2 were scanned during the second trimester (with PET/MR imaging), and 1 was scanne

280 e acetylcholinesterase inhibitors during the second trimester, with hazard ratios of 1.3 (95% confide

281 exposure to an influenza epidemic during the second trimester would increase the risk for adult major

282 ounger than 8 GW, older than 10-12 GW, or in second trimester xenografted testes (14-17 GW).