ライフサイエンスコーパス: neonate

1 th while ensuring energy availability to the neonate.

2 ed consent on behalf of themselves and their neonate.

3 peripheral physiology and development of the neonate.

4 ntestinal macrophages was also unique to the neonate.

5 tones and spatial olfactory memory in Ts1Cje neonates.

6 pregnancy-associated cases (87%) occurred in neonates.

7 evelopment of a vaccine that is effective in neonates.

8 0.87), and IAT (0.64; 95% CI: 0.42, 0.86) in neonates.

9 I2 = 0%, p = 0.09) versus glyburide-exposed neonates.

10 ught to have a benign course in asymptomatic neonates.

11 lipid profile and small-for-gestational-age neonates.

12 llow-up data were available for 99.2% of the neonates.

13 , including respectful care, for mothers and neonates.

14 of general anesthesia in young children and neonates.

15 0.07-1.53, p = 0.03) versus insulin-exposed neonates.

16 L in 80% of term neonates and 82% of preterm neonates.

17 ell as late sPTB, late pi-PTB and early term neonates.

18 host defence mechanism against infection in neonates.

19 ons result in serious respiratory defects in neonates.

20 I 0.45-0.79, p < 0.001) than insulin-exposed neonates.

21 myeloid cells and macrophages compared to WT neonates.

22 were female and 3 underwent ROP treatment as neonates.

23 atic neonates with SDH compared with control neonates.

24 age to the tissues resulting in death of the neonates.

25 nt of presumptive HIV treatment in high-risk neonates.

26 ure causing partial lethality of embryos and neonates.

27 le-dose groups within 7 days of birth in the neonates.

28 us disease in immunocompromised patients and neonates.

29 omparisons were made with full-term 14-d-old neonates.

30 eonates with subdural hemorrhage and control neonates.

31 with ZIKV without microcephaly or uninfected neonates.

32 ased in VPT neonates compared with full-term neonates.

33 e intestinal microbiota and immune system in neonates.

34 Study participants included 1734 preterm neonates.

35 rformed in neonates matched 1:1 with control neonates.

36 ting late-onset sepsis in moderately preterm neonates.

37 pha, CRP, sCD14, and BAFF than United States neonates.

38 lk of GABA(A)Rs in oligodendrocytes from rat neonates.

39 n than Casp8(C362A/C362A)Mlkl(-/-)Casp1(-/-) neonates.

40 f host-directed immunotherapies dedicated to neonates.

41 We included 255 women and their 260 fetuses/neonates.

42 omparable in HIV-exposed and non-HIV-exposed neonates.

43 al immunization with DeltagD-2 would protect neonates.

44 been used as a proxy for the iron status of neonates.

45 he K1 antigen is a leading cause of death in neonates.

46 a devastating gastrointestinal emergency of neonates.

47 macrosomia, and large for gestational age in neonates.

48 equencies were markedly lower in the preterm neonates.

49 to -0.01, p = 0.03) versus glyburide-exposed neonates.

50 c inflammation in late gestation fetuses and neonates.

51 gin breastfeeding on demand than full weight neonates.

52 on the outcomes of preterm, low-birth-weight neonates.

53 more severe and disseminated infection in WT neonates.

54 ctices that might constitute mistreatment of neonates.

55 tations are typically limited, especially in neonates.

56 The rate of CMV-related HL was 8 per 11 887 neonates (0.7 per 1000 live births).

57 onate (1.1%) in the intervention group and 1 neonate (1.0%) in the control group developed an S aureu

58 ain (HR, 0.57 [95% CI, 0.31 to 0.88]), and 1 neonate (1.1%) in the intervention group and 1 neonate (

59 he intervention and placebo groups, 13 of 89 neonates (14.6%) and 29 of 101 neonates (28.7%), respect

60 Delayed cord clamping was done for most neonates (1493 [91.8%] of 1627); other practices, such a

61 Among 236 randomized neonates, 208 were included in the analytic sample (55%

62 , 18 305 were children (77.7%) and 5267 were neonates (22.3%).

63 primary outcome event occurred in 154 of 563 neonates (27.4%) in the LMA group and 144 of 591 (24.4%)

64 ups, 13 of 89 neonates (14.6%) and 29 of 101 neonates (28.7%), respectively, acquired concordant S au

65 A total of 28 of 89 neonates (31.4%) in the intervention group and 46 of 101

66 d 6 mg/kg twice daily thereafter for preterm neonates (34 to <37 weeks gestational age).

67 us excitatory postsynaptic currents in young neonates (-34.4%).

68 Half of enrolled neonates (50.4%) had suspected sepsis; 40.8% of cultures

69 d on a 3T scanner in 138 sleeping nonsedated neonates: 55 full-term neonates (gestational age >= 36 w

70 d vaginally compared with 157 of 254 control neonates (62%, 95% CI: 56, 68; P < .001).

71 r major bleeding and/or mortality in preterm neonates (7% absolute-risk reduction).

72 s between the neonatal SDH group and control neonates (730 cm(3) +/- 85 and 742 cm(3) +/- 76 at 2 yea

73 Two hundred ninety-seven neonates (88.3%) died in the delivery room.

74 In vaginally delivered neonates, a surge of AVP is released into the bloodstrea

75 cture of the fecal microbiota in mothers and neonates according to maternal H. pylori status and deli

76 at Jundiai University Hospital and from the neonates after delivery.

77 maternal infection or immunization protects neonates against infection with an attaching and effacin

78 r maternal antibodies to pups, which protect neonates against ZIKV infection.

79 ional diffusion tensor imaging of 89 preterm neonates aged 31-42 postmenstrual weeks.

80 ons such as developmental stage, exposure of neonate and adults to dsRNA, exposure of adults to diffe

81 ing pregnancy seems safe for both mother and neonate and is likely to be helpful, especially before d

82 s of a monochorionic placenta, and between a neonate and its associated placenta.

83 There were 2,419 neonates and 10,687 nonneonates from 22 hospitals.

84 longed critical illness mortality was 24% in neonates and 8% in nonneonates (vs 5% and 0.4%, respecti

85 centrations exceeded 3 mug/mL in 80% of term neonates and 82% of preterm neonates.

86 Nkx6.2-null embryos, neonates and adult mice exhibited alterations of locomot

87 and cellular composition of the pancreas in neonates and adults in healthy and diseased conditions u

88 irths, stillbirths, and severe infections in neonates and adults.

89 Cross-sectional and cohort studies of neonates and children aged <21 years old were eligible f

90 characteristics of the haemostatic system in neonates and children are significantly different compar

91 f death in stillborn fetuses and in deceased neonates and children younger than 5 years, to inform ch

92 pies in the management of hyperammonaemia in neonates and children.

93 hybrid therapy) to manage hyperammonaemia in neonates and children.

94 at allowed for 2D (1)H-(13)C NMR of D. magna neonates and exhibited (1)H sensitivity (nLOD(omega)(600

95 crocephaly and other neurological defects in neonates and Guillain-Barre syndrome in adults.

96 esvirus capable of causing severe disease in neonates and immunocompromised patients.

97 optimal target levels of anticoagulation for neonates and infants and lack of suitable drug formulati

98 35 and greater than or equal to 10 days for neonates and nonneonates, respectively.

99 o 28 weeks' gestation and DNA methylation in neonates and whether a dietary and physical activity int

100 us system (CNS) infection among hospitalized neonates and young infants, yet testing for PeV is not r

101 es in children impacted care of hospitalized neonates and young infants.

102 sation in any neonates; neutropenia (25 [6%] neonates) and anaemia (six [1%]) were most common.

103 ines and were evaluated for SDH at baseline (neonates) and at ages 1 and 2 years.

104 ng development, prenatal stages, lost in the neonate, and adult heart confirmed by qRT-PCR and in sit

105 ld enable opioid screening, particularly for neonates, and points to the potential for pharmacokineti

106 s of death for children, children with ALRI, neonates, and preterm neonates using mixed-effects logis

107 e changes in oxygen tension, particularly in neonates, and that subsequent degranulation may contribu

108 via PPARalpha in response to lipids in mice (neonates- and food-restricted adults).

109 p = 0.026) but not preterm/low-birth-weight neonates (aOR 1.30; 95% CI 0.76-2.23; p = 0.366).

110 Neonates are at increased risk for bacterial sepsis.

111 Neonates are particularly susceptible to infection.

112 Extremely preterm neonates are particularly susceptible to infections, lik

113 of specific frontolimbic pathways in preterm neonates as early as term-equivalent age.

114 gnancy cohort, ZIKV RT-PCR positivity in the neonate at birth is strongly associated with microcephal

115 nitiated within 48 h of birth in HIV-exposed neonates at high risk of HIV acquisition.

116 pine for very early treatment of HIV-exposed neonates at high risk of HIV acquisition.

117 Neonates at risk of childhood atopy and asthma exhibit p

118 (3 mug/mL) in 314 (90%, 95% CI 86-93) of 349 neonates at week 1 and 174 (87%, 81-91) of 201 at week 2

119 We then ranked the neonates based on their predicted baseline risk and cate

120 from 5695 pairs of non-diabetic mothers and neonates between 1 Jan 2014 and 31 Dec 2014.

121 Among neonates born at "term" who are admitted to a PICU, incr

122 ended routine probiotics supplementation for neonates born before 34 completed weeks of gestation.

123 A total of 11 900 neonates born from a population with >=97% maternal sero

124 Neonates born to metformin-treated mothers had lower bir

125 nes were up-regulated in the hypothalamus of neonates born to obese mothers.

126 These associations were stronger in female neonates but only persisted in girls between fasting glu

127 e- or small-for-gestational age (LGA or SGA) neonate by BMI group.

128 inuous, one-to-one observations of women and neonates by independent data collectors.

129 these neonatal care practices, maternal and neonate characteristics, and maternal mistreatment.

130 s, scaled to various sizes representative of neonates, children, and adults, with varying injury seve

131 terior and posterior CB was increased in VPT neonates compared with full-term neonates.

132 he age of 2 years were robustly predicted by neonate cortical microstructure using support vector reg

133 Early neonate deaths, stillbirths, and higher order multiple b

134 Despite equivalent circulating levels, neonates demonstrate lower presence of monocytes inside

135 Four (14%) neonates developed kernicterus between days 14 and 45 po

136 A high proportion of neonates did not receive recommended care practices, and

137 to improve the quality of care for women and neonates during childbirth, there is growing interest in

138 (GBS) can result in vertical transmission to neonates during labor/delivery.

139 cardio-respiratory events (CRE), in preterm neonates during postnatal transition.

140 portance of providing protective immunity to neonates during this window of vulnerability.

141 We included data for 362 women-neonate dyads (356 [98%] with available data for neonata

142 tment of human extremely low gestational age neonates (ELGAN) with extremely low birth weight (ELBW;

143 d 50 mg/L PS-NPs until the production of the neonates (F1) followed by a two-generation recovery.

144 ere the potential sites of action are in the neonate for these robust levels of circulating AVP at bi

145 epigenome-wide association studies of 8,825 neonates from 24 birth cohorts in the Pregnancy And Chil

146 s were observed in pancreases of fetuses and neonates from prepregnant HF-fed dams.

147 8 sleeping nonsedated neonates: 55 full-term neonates (gestational age >= 36 weeks) and 83 VPT neonat

148 tes (gestational age >= 36 weeks) and 83 VPT neonates (gestational age < 30 weeks).

149 age and mortality in hospital for term-born neonates (>= 37 wk') admitted to PICUs in Australia and

150 rapine dosed at 6 mg/kg twice daily for term neonates (>=37 weeks gestational age) or 4 mg/kg twice d

151 Glyburide-exposed neonates had a nonsignificant increase in total fat mass

152 Although HIV-exposed neonates had altered MBC subset distributions, detection

153 All the neonates had an estimated gestational age of at least 34

154 Thirty-six neonates had CBH: 14 (6%) with only punctate CBH and 22

155 Metformin-exposed neonates had decreased ponderal index (-0.09 kg/m3, 95%

156 Metformin-exposed neonates had decreased ponderal index (-0.13 kg/m3, 95%

157 Kenyan neonates had higher levels of IP-10, TNF-alpha, CRP, sCD

158 In total 5 (11% [95% CI, 4%-24%]) neonates had prolongation of the QTc >2 SD above histori

159 living human fetuses and in prematurely born neonates have provided insight into the staged processes

160 ient Sample database was queried to identify neonates hospitalized for endogenous endophthalmitis bet

161 ssion of the type I IFN receptor relative to neonate IECs, and the response of IEC organoids to type

162 sible to induce transplantation tolerance in neonates, immune tolerance strategies have been actively

163 o the immaturity of their immune system, and neonate immunization is potentially unsafe.

164 Septicemia is a leading cause of death among neonates in low-income settings, a situation that is det

165 5.6% neonates in our study were SGA.

166 infection including meningitis and AMR among neonates in sub-Saharan Africa and assessed the quality

167 Death within 7 days occurred in 21.7% of the neonates in the LMA group and 18.4% of those in the face

168 Among 190 neonates included in the analysis, 74 (38.9%) acquired S

169 physiological injury aspects are distinct in neonates, including immune signaling.

170 ever, analysis of dopamine concentrations of neonates indicates that endogenous levels of spinal dopa

171 s) using next-generation sequencing (NGS) in neonates, infants, and children can provide valuable ins

172 Furthermore, direct vaccination of neonates is likely ineffective due to the immaturity of

173 The gut of healthy human neonates is usually devoid of viruses at birth, but quic

174 to prevent the bloodstream infections in the neonates, it is indispensable to diagnose the disease pr

175 Neonates kicked with an adult-like number of temporal ac

176 ex virus (HSV) can cause severe infection in neonates leading to mortality and lifelong morbidity.

177 Recent data have highlighted how the naive, neonate-like immune system of specific pathogen-free mic

178 To investigate mortality in periviable neonates <=23 weeks gestational age and calculate its im

179 Neonates (<28 days; n = 1650) hospitalized for endogenou

180 n be reliably detected in blood samples from neonate male turtles but not females and can be used as

181 A secondary analysis was performed in neonates matched 1:1 with control neonates.

182 ties of the T cell compartment in ELGAN/ELBW neonates may at least partially explain their increased

183 Results A total of 311 neonates (mean gestational age +/- standard deviation, 3

184 , 39.6 weeks +/- 1.2) and 55 matched control neonates (mean gestational age, 39.7 weeks +/- 1.2).

185 agnetic resonance images of 221 very preterm neonates (median gestational age = 27.9 weeks) were manu

186 These phenotypes are mirrored in neonate mice overexpressing IL-23 in CX3CR1(+) myeloid c

187 To fully understand neonate microbial colonization, we need to study the int

188 Neonates (n = 236) with S aureus-colonized parent(s) wer

189 regnant women with ITP (pregnancies, n = 17; neonates, n = 18) treated with either eltrombopag (n = 8

190 did not lead to nevirapine cessation in any neonates; neutropenia (25 [6%] neonates) and anaemia (si

191 s contribute to post-MI vessel growth in the neonate, none are active during neovascularization after

192 was associated with increased likelihood of neonates not receiving recommended breastfeeding practic

193 h after birth, separation of the mother and neonate occurred in 844 (51.9%) of 1627 cases; and was m

194 age between 28 days and 1 year (compared to neonates, odds ratio [OR] = 3.58, p < 0.05), underlying

195 Neonates of different species are born with a set of pre

196 OR] 1.38, 95% CI 1.01-1.89, p = 0.04) versus neonates of insulin-treated mothers.

197 5% CI -0.26 to 0.00, I2 = 0%, p = 0.04) than neonates of insulin-treated mothers.

198 Overall, birthweight was higher among neonates of women randomly assigned to sulfadoxine-pyrim

199 Neonates often develop poor immunity against intracellul

200 illatory ventilation in adults compared with neonates on the basis of lung size, using a computationa

201 ESBL-E carriers and with the total number of neonates on the same ward.

202 sociated with an increased risk of death for neonates overall (aOR 1.45; 95% CI 1.04-2.00; p = 0.026)

203 ed to chemotherapy compared with non-exposed neonates (p=0.035).

204 we need to study the interacting effects of neonate, parents, nest, and external environment.

205 In 2019, 128 H. zea neonates per isofamily for a total of 114 F(2) families

206 Birthweight percentiles were lower in neonates prenatally exposed to chemotherapy compared wit

207 t time, adult size, lifespan, fecundity, and neonate production.

208 compensatory mechanisms to boost immunity in neonates, providing insights for maternal vaccine design

209 he trial continued comparing BCG-Japan (3191 neonates randomized, 3184 analyzed) with BCG-Russia (317

210 functional profile expressed in OLs from the neonate rat.

211 Antibiotic treatment of neonates restored LPS-induced small intestinal cell shed

212 is successful in children and adults but in neonates results in frequent restenosis.

213 Many maternal traits are associated with a neonate's gestational duration, birth weight, and birth

214 We tested whether optimizing the neonate's microbiome through maternal probiotic suppleme

215 dual neonates, we calculated deviations of a neonate's observed MRI from that predicted by the model

216 In CB serum of healthy neonates, S100A12 was found to be higher in female newbo

217 local tissue shape in a large cohort of 408 neonates scanned cross-sectionally across the perinatal

218 ally connected to proto language networks in neonates scanned within one week of birth.

219 milk begins its passage toward the dependent neonate, seconds after the command.

220 or maternal age, smoking, parity, ethnicity, neonate sex, and predicted cell-type composition.

221 marital status, neonate weight at birth, and neonate sex] 1.8, 95% CI 1.3-2.6) than those who were ma

222 tic resonance imaging (fMRI), and found that neonates showed similar functional connectivity patterns

223 s, different 3(rd) instar larva tissues, and neonate starvation.

224 However, on the ground neonates stepped with fewer temporal patterns but all st

225 tcome was more strongly noted in the sickest neonates, such as those requiring extracorporeal life su

226 n the first trimester, up to 30% of infected neonates suffer long-term sequelae.

227 )Casp11(-/-) (Casp11 is also known as Casp4) neonates survived more often than Casp8(C362A/C362A)Mlkl

228 that the assembly of the viral community in neonates takes place in distinct steps.

229 Of the 409 neonates tested, 19 (4.6%) were ZIKV RT-PCR positive in

230 ons of macrophages and Ly6C(hi) monocytes in neonates that express high levels of TLR9 and low levels

231 ells seemed normal in the ELGAN/ELBW preterm neonates, their expression of the homing receptors alpha

232 with screening for retinal tumors in at-risk neonates (those inheriting RB1 pathogenic alleles from a

233 oss-resistance to Cry2Ab, and developed from neonate to adult on Bt cotton producing Cry1Ac.

234 cktip reef shark (Carcharhinus melanopterus) neonates to climate change relevant changes in temperatu

235 iously unknown genetic mechanism that allows neonates to respond to infections as efficiently as adul

236 Parents may expose neonates to S aureus colonization, a well-established pr

237 ime, greatly enhances our ability to measure neonate turtle sex ratios at population levels across ne

238 ribe a new technique used to identify sex in neonate turtles of two TSD species, a freshwater turtle

239 ing these approaches, namely vaccinating the neonate under the cover of vertically transferred matern

240 study aims to describe the care received by neonates up to 2 h after birth in a sample of three coun

241 n, children with ALRI, neonates, and preterm neonates using mixed-effects logistic regression.

242 es for metabolites monitoring in infants and neonates using saliva as a noninvasive sample.

243 eks, there were 140 and 130 admissions among neonates vaccinated with BCG-Denmark and BCG-Russia, res

244 urological impairment was present in 9.4% of neonates versus 48.8% of children at discharge compared

245 cilitates immune tolerance preferentially in neonates via induction of antigen-specific regulatory T

246 Net transfer of iron to the neonate was higher in women with lower total body iron (

247 The pooled prevalence among neonates was 27.0% (95% CI: 22.1%-33.1%) among children

248 onates with cCMVI compared to CMV-uninfected neonates was 89.5 (95% CI, 39.7-202.0).

249 ence of hospital-acquired pressure ulcers in neonates was 9.8% (95% CI: 2.9%-19.8%) and in children a

250 ncentration of 12,13-diHOME in the faeces of neonates was found to be associated with an increased pr

251 ments were conducted when only the midgut of neonate WCR was evaluated from the same treatments.

252 In individual neonates, we calculated deviations of a neonate's observ

253 ons on outcomes of preterm, low-birth-weight neonates, we found moderate to high evidence for the sup

254 ry, maternal age, education, marital status, neonate weight at birth, and neonate sex] 1.8, 95% CI 1.

255 Metformin-exposed neonates were born lighter (-191.73 g, 95% CI -288.01 to

256 Metformin-exposed neonates were born lighter (-73.92 g, 95% CI -114.79 to

257 PBMCs from ELGAN/ELBW neonates were collected at day 14, day 28, and postmenst

258 Between Jan 23, 2015, and Sept 4, 2017, 438 neonates were enrolled and included in analyses; 36 had

259 Glyburide-exposed neonates were heavier at birth (58.20 g, 95% confidence

260 0.6%; 95% confidence interval [CI], 0.4-0.7) neonates were identified with cCMVI.

261 Metformin-exposed neonates were lighter with reduced lean mass versus insu

262 roviders within 1 h before childbirth, their neonates were more likely to be slapped (AOR 1.9, 1.1-3.

263 Healthy neonates were randomized 1:1 to BCG-Denmark (2851 random

264 We describe a neonate who presented with hydrocephalus, necrotizing ce

265 Neonates who did and did not receive ECLS were matched b

266 ve been impacted by this epidemic, including neonates who exhibit Neonatal Abstinence Syndrome (NAS).

267 Integrating targeted cCMVI screening among neonates who fail a HS could be a reasonable, cost-effec

268 iority trial in Uganda, we randomly assigned neonates who required positive-pressure ventilation to b

269 All neonates who required the mattress to provide a temperat

270 Participants were neonates who were at least 34 weeks gestational age at b

271 model, we calculated model deviations in 46 neonates who were scanned on a second occasion.

272 Here we aimed to evaluate the neonate whole-brain cortical microstructure quantified b

273 en 33 and 34 degrees C during TH compared to neonates with a favourable outcome.

274 We report five unrelated neonates with a lethal metabolic disorder characterized

275 Neonates with a low birthweight (<2.5 kg) were more like

276 ndomisation to glyburide resulted in heavier neonates with a propensity to increased adiposity versus

277 Neonates with an unfavourable outcome require less cooli

278 an LMA reduces mortality and morbidity among neonates with asphyxia is unknown.

279 In neonates with asphyxia, the LMA was safe in the hands of

280 as approximately a 2-5 fold risk of birthing neonates with birthweights under the 3(rd), 5(th), 10(th

281 to disease severity and clinical outcomes in neonates with BPD.

282 assay is an accurate method for identifying neonates with cCMV infection and, given its simplicity,

283 The prevalence ratio of HL among neonates with cCMVI compared to CMV-uninfected neonates

284 Of the 62 neonates with cCMVI who underwent a complete hearing eva

285 ess mortality for low- and intermediate-risk neonates with CDH.

286 ewborn hearing screening (HS) in identifying neonates with CMV-related HL.

287 Germ-free mice were colonized as neonates with either a simplified human infant microbiot

288 Neonates with HIE display impaired thermoregulation, res

289 unchanged in a sensitivity analysis in which neonates with missing data were counted as having had a

290 Twenty-eight neonates with moderate or severe HIE treated with TH wer

291 ker and predictor of injury and mortality in neonates with moderate or severe HIE.

292 the long-term neurodevelopmental outcome of neonates with moderate to severe HIE.

293 We hypothesized that neonates with more severe brain injury on magnetic reson

294 Neonates with postmenstrual age 33 to 44 weeks at risk o

295 Fifty-five of 57 neonates with SDH (97%; 95% CI: 92, 100) were delivered

296 The subgroup included 55 neonates with SDH (mean gestational age, 39.6 weeks +/-

297 er volumes, and MRI findings in asymptomatic neonates with SDH compared with control neonates.

298 2 years did not differ between asymptomatic neonates with subdural hemorrhage and control neonates.

299 Neonates without confirmed in-utero HIV infection receiv

300 However, relative to ZIKV-negative neonates, ZIKV-positive infants had a five-fold increase