ライフサイエンスコーパス: neonatal period

1 babies die in the first 4 weeks of life (the neonatal period).

2 proportion developed fatal sepsis during the neonatal period.

3 responses to heterologous stimulants in the neonatal period.

4 icrobiome to dietary substrates in the early neonatal period.

5 t on the detailed timing of death within the neonatal period.

6 the rat are 'primed' by tissue injury in the neonatal period.

7 adherence to low carbohydrate diets, and the neonatal period.

8 equence of pulmonary inflammation during the neonatal period.

9 t optimizing successful breastfeeding in the neonatal period.

10 re, even if they remained healthy during the neonatal period.

11 ed interleukin (IL)-12 production during the neonatal period.

12 velopment of in vivo cytotoxicity during the neonatal period.

13 ty of hepatocytes are once transduced in the neonatal period.

14 o transduce a majority of hepatocytes in the neonatal period.

15 cessive diarrheal disorder presenting in the neonatal period.

16 day 2, and whose mothers were visited in the neonatal period.

17 annel expression normally found in the fetal/neonatal period.

18 is, and hippocampal energy metabolism in the neonatal period.

19 tensive care or factors operating beyond the neonatal period.

20 od, the risk for seizures is greatest in the neonatal period.

21 sue during the period of rapid growth in the neonatal period.

22 y skewed inactivation, especially during the neonatal period.

23 hypsarrhythmia if only recorded in the post-neonatal period.

24 ective in preventing contractures beyond the neonatal period.

25 s serious morbidity and mortality during the neonatal period.

26 stage-dependent manner permissive during the neonatal period.

27 l lambs but then disappears during the later neonatal period.

28 ol of respiratory motor pattern in the early neonatal period.

29 pensate for ACTA1 abnormalities in the fetal/neonatal period.

30 %) of double-homozygous mice died during the neonatal period.

31 in babies who were not breastfed during the neonatal period.

32 irculating levels of sex steroids during the neonatal period.

33 b responses to viruses of infants beyond the neonatal period.

34 permeability barrier maturation in the early neonatal period.

35 ch none of the affected children died in the neonatal period.

36 nvariably fatal course when diagnosed in the neonatal period.

37 N370S homozygosity was lethal in the neonatal period.

38 ts, 3,010 were diagnosed with HIE during the neonatal period.

39 in rapidly growing normal tissues during the neonatal period.

40 ccumulate VLCFA, but they present during the neonatal period.

41 s to be a universal phenomenon unique to the neonatal period.

42 T cells, is also rapidly acquired within the neonatal period.

43 result of priming of splenocytes within the neonatal period.

44 enge with the same Ag encountered during the neonatal period.

45 ndition that afflicts preterm infants in the neonatal period.

46 SP-B background was invariably lethal in the neonatal period.

47 n the murine SP-B-/- background survived the neonatal period.

48 ost common gastrointestinal emergency in the neonatal period.

49 m-negative septicaemia and meningitis in the neonatal period.

50 nd annular tail and paw constrictions in the neonatal period.

51 bacterium that causes meningitis during the neonatal period.

52 A further nine died within the neonatal period.

53 c levels of circulating FVIII throughout the neonatal period.

54 This advantage largely disappeared after the neonatal period.

55 nd require constant attention throughout the neonatal period.

56 supranormal levels of FVIII activity in the neonatal period.

57 Ag-specific effector cells during the actual neonatal period.

58 ly 5% to 10% of band 3 null mice survive the neonatal period.

59 polycystic kidney disease and die during the neonatal period.

60 R-1 and VEGFR-2, most prominently during the neonatal period.

61 one of the TFPI(K1)(-/-) mice survive to the neonatal period.

62 orpuscles after nerve resection in the early neonatal period.

63 seizures, and no patient had seizures in the neonatal period.

64 lar and pustular disorders are common in the neonatal period.

65 nfection of the mouse during the in utero or neonatal period.

66 ring the later gestational stages and in the neonatal period.

67 mice survived to birth, but died during the neonatal period.

68 patients with respiratory failure beyond the neonatal period.

69 or duration of sleep impairments beyond the neonatal period.

70 nal organs of neonates who died later in the neonatal period.

71 en (2.4%) were diagnosed with SNM during the neonatal period.

72 r-fold higher in adulthood compared with the neonatal period.

73 tralogy of Fallot who are symptomatic in the neonatal period.

74 who survived and did not emigrate during the neonatal period.

75 ium showed a gradual increase throughout the neonatal period.

76 oietic stem cells (HSCs) during the fetal to neonatal period.

77 t half of them projected to occur during the neonatal period.

78 we observed a very beneficial effect in the neonatal period.

79 for infants with severe infection during the neonatal period.

80 ls of total serum bilirubin (TSB) during the neonatal period.

81 aternity leave were concentrated in the post-neonatal period.

82 r cystic periventricular leukomalacia in the neonatal period.

83 pment of the somatosensory cortex during the neonatal period.

84 under-5 deaths, 2.7 million occurred in the neonatal period.

85 ment in shaping cortical activity during the neonatal period.

86 injury within a brief temporal window in the neonatal period.

87 s disorders of gastrointestinal tract during neonatal period.

88 s causes and 44% (2.761 million) died in the neonatal period.

89 by life-threatening bleeding episodes in the neonatal period.

90 cuate nucleus of the hypothalamus during the neonatal period.

91 d extensive in situ proliferation during the neonatal period.

92 respectively, more likely to die during the neonatal period.

93 milar studies do not exist for the fetal and neonatal period.

94 icy of transatrial repair delayed beyond the neonatal period.

95 hy of prematurity (ROP) was performed in the neonatal period.

96 with both characteristics extend beyond the neonatal period.

97 sopressors and blood transfusions during the neonatal period.

98 orn premature and required intubation during neonatal period.

99 caused by pulmonary hypoplasia in the early neonatal period.

100 rom white matter injury sustained during the neonatal period.

101 nsates for the lack of MZ B cells during the neonatal period.

102 the clinical approach to neutropenia in the neonatal period.

103 on thymic development may extend beyond the neonatal period.

104 neonatal bacteremia was 3.0 per 1000 person-neonatal periods.

105 d autonomic ganglia during the embryonic and neonatal periods.

106 eart regeneration, particularly in fetal and neonatal periods.

107 owest compared with WHO standards during the neonatal period (-1.4 cm/month for girls and -1.6 cm/mon

108 the first to document that during the early neonatal period, (1) both VEGF and bFGF modulate capilla

109 ons were diagnosed with diabetes outside the neonatal period (12-46 years).

110 21 SCID infants with transplantations in the neonatal period, 20 (95%) survive.

111 ughout pregnancy, during delivery and in the neonatal period; (3) provided that their myasthenia is u

112 roportion of child deaths that occurs in the neonatal period (38% in 2000) is increasing, and the Mil

113 e excessive accumulation of TSB in the early neonatal period (5 days after birth) promotes activation

114 of the malformation is generally done in the neonatal period, a randomised clinical trial to assess i

115 s by transient gastric irritation during the neonatal period, a time of known neuronal vulnerability

116 During the neonatal period, activity-dependent neural-circuit remod

117 In four cases, diabetes presented in the neonatal period (age at diagnosis 1-7 days).

118 38% (MRR, 0.62; 95% CI, .46-.83) within the neonatal period and 16% (0.84; .71-1.00) by age 12 month

119 ollowing a transient noxious stimulus in the neonatal period and a potentially important role for TRP

120 ; 80 in control clusters), 77 died after the neonatal period and before 18 months (31 in intervention

121 consisted of transcripts that peaked in the neonatal period and contained a number of retrotransposo

122 developed unexpected hypoornithinemia in the neonatal period and died 24 to 48 hours after birth.

123 y, with cost differences concentrated in the neonatal period and during the first year of life.

124 emia and offspring AA measured by MRI in the neonatal period and during the preschool years.

125 erammonemia of unexplained origin during the neonatal period and early childhood.

126 hospital resources, particularly during the neonatal period and first year of life.

127 Of the live births, 13 died in the neonatal period and four were lost to follow up.

128 ster, carries a substantial mortality in the neonatal period and frequently requires pacing.

129 otte's and Hammersmith Hospital in the early neonatal period and imaged at a median corrected age of

130 throughout life but more actively during the neonatal period and in response to demyelinating insults

131 t thymic B cell activation starts during the neonatal period and is characterized by TCR/CD40-depende

132 tory hair cells is possible during the early neonatal period and may exist to a very limited degree a

133 of seizures during lifetime is found in the neonatal period and neonatal seizures lead to a propensi

134 that appear as soon as hair develops in the neonatal period and persist throughout life.

135 Resident hCPCs are most abundant in the neonatal period and rapidly decrease over time.

136 eases rapidly in a linear pattern during the neonatal period and slows progressively with age.

137 infants receiving the first dose during the neonatal period and the second before 60 days of age.

138 the Damus-Kaye-Stansel procedure beyond the neonatal period and those had subaortic resection.

139 have adverse health consequences during the neonatal period and throughout adult life.

140 otropic hormone (ACTH) production during the neonatal period and was rescued by ACTH replacement.

141 of LXR activators on SC acidification in the neonatal period and whether these activators correct the

142 nsequences for health in mammals both in the neonatal period and, as a result of fetal programming, i

143 d ROP not deemed to require treatment in the neonatal period, and 13% of eyes (30) had neonatal cryot

144 ication of new causes of hypertension in the neonatal period, and improved insights into therapy.

145 les (taken at several time points during the neonatal period, and in infancy) from 596 full-term babi

146 ions of hemoglobin and hematocrit during the neonatal period, and increased serum ferritin levels and

147 osition of the gut microbiota throughout the neonatal period, and into infancy.

148 ecipients were deprived of ovarian Ag in the neonatal period, AOD was suppressed by female but not by

149 malities during pregnancy, delivery, and the neonatal period are associated with adult-onset schizoph

150 the majority of childhood deaths in the post-neonatal period are caused by infections that can be eff

151 ntitative magnetic resonance measures in the neonatal period are related to performance at 2 years.

152 Elevated creatine kinase levels in the neonatal period are the initial screening marker in DMD

153 mic the human disease and survive beyond the neonatal period, are needed.

154 lood concentrations of BR, especially in the neonatal period, are treated with blue-green light photo

155 hCPC proliferation was greatest during the neonatal period as evidenced by c-kit(+) Ki67(+) express

156 primary treatment for coarctation beyond the neonatal period as well as for muscular ventricular sept

157 During the neonatal period, Ascl1 expression was detected in progen

158 ural brain abnormalities in the prenatal and neonatal periods associated with genetic risk for schizo

159 s containing the lacZ marker gene during the neonatal period at a time before T-cell maturation had o

160 nditions compatible with survival beyond the neonatal period because of termination of such pregnanci

161 pithelial cells (mTECs) during the embryonic-neonatal period being both necessary and sufficient to e

162 e to mercury during the prenatal period, the neonatal period (birth to 28 days), and the first 7 mont

163 In junctions denervated in the neonatal period both gutter formation and the disappeara

164 al to the maturation of aerodigestion in the neonatal period but also unlikely to co-occur with imita

165 diabetes that are often diagnosed during the neonatal period but may present later.

166 e partially independent of ROP status in the neonatal period but reports similar overall visual funct

167 at encodes matriptase, not only survived the neonatal period but were healthy and displayed normal lo

168 ative bacteria causing meningitis during the neonatal period, but is unclear what microbial factors m

169 often fatal when its onset occurs during the neonatal period, but it is milder when onset occurs late

170 ichia coli meningitis commonly occurs in the neonatal period, but the basis of this age dependency is

171 g defense against bacterial pneumonia in the neonatal period, but the signals that guide pulmonary IL

172 During the neonatal period, calcitriol-stimulated intestinal calciu

173 dents suggests that tissue damage during the neonatal period can "prime" developing nociceptive pathw

174 s of inspired supplemental oxygen during the neonatal period can also lead to oxygen toxicity if oxyg

175 s demonstrate that gastric irritation in the neonatal period can result in chronic gastric hypersensi

176 nt at birth and numbers decreased during the neonatal period; CD3(+)4(+)8(+) T cells were present in

177 ardiomyocytes exit the cell cycle during the neonatal period, commensurate with the loss of regenerat

178 control group were stillborn or died in the neonatal period compared with 221 (15%) of 1447 infants

179 e increased respiratory morbidity during the neonatal period compared with full term-born (39-42 week

180 o 0.25, 95% CI 0.12-0.53; 13 infections/4839 neonatal periods) compared with dry cord-care clusters (

181 mplications to mortality decreased after the neonatal period; congenital abnormalities remained an im

182 mice lacking skeletal actin die in the early neonatal period (day 1 to 9).

183 tistically significant relation later in the neonatal period (days 2-6 1.36, 0.84-2.21; days 7-27 1.1

184 e leading causes of death for early and late neonatal period deaths, respectively.

185 osahexaenoic acid supplementation during the neonatal period did not significantly improve bronchopul

186 All 7 patients diagnosed in the neonatal period died (median age 1 day).

187 or, exendin-4 (Ex-4), during the prediabetic neonatal period dramatically prevents the development of

188 Maternal separation (MS) during the neonatal period enhances stress responsivity in adulthoo

189 owever, the islets in the mutant mice in the neonatal period exhibited morphological defects in organ

190 us for the Hs2st gene trap allele die in the neonatal period, exhibiting bilateral renal agenesis and

191 ved for infants receiving transplants in the neonatal period (first 28 days of life), prior to the de

192 ertriglyceridemia and fatty liver during the neonatal period, followed by development of a peripheral

193 e, sufficient plasticity persists during the neonatal period for late-stage myelination to occur.

194 sessed relative to control rats in the early neonatal period for mast cell and microglia activation w

195 eic, related hematopoietic stem cells in the neonatal period had higher levels of T-cell reconstituti

196 Those who survived the neonatal period had late survival, pulmonary artery pres

197 environmental fluctuations during the early neonatal period had sustained effects on the developing

198 The neonatal period has been thought of as a window in ontog

199 s, self-antigens, or vaccination--during the neonatal period has dramatic effects on the adult Ab res

200 rinatal lung disease to children outside the neonatal period has important potential pitfalls.

201 Additionally, risk of death beyond the neonatal period has not yet been reported for offspring

202 ncy and intrapartum and to the infant in the neonatal period has resulted in a reduction of the overa

203 All patients who survive the neonatal period have at least one amino acid substitutio

204 fficacy of supplementation of infants in the neonatal period have inconsistent results.

205 Recurrent brief seizures during the neonatal period have long-term detrimental effects on be

206 th Escherichia coli K1 meningitis during the neonatal period have remained significant over the last

207 y provides benefits during the perinatal and neonatal period; however, it may not provide additional

208 could be treated by gene therapy during the neonatal period if prenatal diagnoses are made and the a

209 han 5 years (henceforth, under 5) and in the neonatal period in 2035 for Countdown countries if trend

210 experimental hyperleptinemia induced in the neonatal period in Mc4rPVH and WT mice, but not in the M

211 acteraemia, inflammation, or both during the neonatal period in preterm infants is associated with ad

212 ef exposure to high-dose estrogen during the neonatal period in rats leads to permanent, lobe-specifi

213 during the third trimester-equivalent (i.e., neonatal period in rats).

214 at BSCC may be performed any time beyond the neonatal period in symptomatic patients and may be delay

215 uscular, low pH saline injections during the neonatal period in the development and maintenance of vi

216 e management of opioid withdrawal during the neonatal period in these infants, but less substantive w

217 d 663 (79%) deaths occurred during the early neonatal period, in the first week of life (0-6 days).

218 chemic stroke occurring in the perinatal and neonatal period, including cerebrovascular events that a

219 ely 10% of the GalTase-null mice survive the neonatal period indicates the presence of a previously u

220 stion: Is reduced global brain growth in the neonatal period inevitable after premature birth, or is

221 In all 70 young rats who survived the neonatal period, infarct size (Infarct mass/Risk area x

222 ure of rats to high-dose estrogen during the neonatal period interrupts prostate development in a lob

223 hat longitudinal growth during the fetal and neonatal periods involves depletion of chondroprogenitor

224 Early mortality for cardiac surgery in the neonatal period is approximately 10% and beyond infancy

225 xposure to broad spectrum antibiotics in the neonatal period is associated with persistent alteration

226 s demonstrate that ventilatory output in the neonatal period is critically dependent on serotonin neu

227 The neonatal period is crucial for the early microbial colon

228 dose schedule with the first dose during the neonatal period is efficacious in preventing RV-GE in ru

229 ure to endogenous ovarian Ag confined to the neonatal period is insufficient for the induction and ma

230 However, evidence on mortality beyond the neonatal period is limited, especially in North America.

231 ne-based antiretroviral regimen in the early neonatal period is needed.

232 role in controlling this pathway during the neonatal period is of academic importance and immediate

233 ablishment of the microbiome in the critical neonatal period is potentially foundational for lifelong

234 tion of the serotonin transporter during the neonatal period is sufficient to produce impairments in

235 ly neonatal death, but the impact beyond the neonatal period is unclear.

236 function.SIGNIFICANCE STATEMENT The fetal to neonatal period is well known as a critical stage in bra

237 In the neonatal period, it is an uncommon agent of meningitis.

238 tex.SIGNIFICANCE STATEMENT Stroke during the neonatal period leads to long-term disabilities.

239 Introduction of MSG during the neonatal period leads to the NAFLD development in the 4-

240 -control difference was most apparent in the neonatal period (< or =1 month); 18% of controls and 24%

241 evelopment of the gut microbiota, during the neonatal period (<=1 month), remain controversial(3,4).

242 The neonatal period marks an important time in mammalian imm

243 xposure to foreign proteins beginning in the neonatal period may alter or ablate the immune response.

244 upregulation of the miR-15 family during the neonatal period may be an important regulatory mechanism

245 of a relatively common infection during the neonatal period may be long lasting, and the prognosis f

246 herapy or frequent protein injections in the neonatal period might induce tolerance to subsequent inj

247 that all gene-positive cases present in the neonatal period (occasionally prenatally) and that clona

248 rotonergic), contain 5-HT transiently in the neonatal period of development.

249 ion of gut-associated lymphoid tissue in the neonatal period of life.

250 Certain parameters of the neonatal period of the child and the mother were retrosp

251 Immunization during the neonatal period often results in Th2-biased secondary re

252 he effect of inadequate vitamin A during the neonatal period on lung status is still unknown.

253 Delaying the use of PCR until after the neonatal period or repeating PCR on independent samples

254 ed to ETS during gestation, during the early neonatal period, or both.

255 ization by injection of the virus during the neonatal period permits long term gene therapy by repeat

256 However, these mice recover during the neonatal period, presumably as a result of in vivo selec

257 After the neonatal period, primaquine should not be restricted for

258 deling of a 2-dose schedule beginning in the neonatal period projected 1 intussusception event/38,000

259 port here studies of 10 patients who, in the neonatal period, received the diagnosis of hemolysate ep

260 oponents of balloon angioplasty, even in the neonatal period, recognizing the need for reintervention

261 ve dynamics of GABAergic neurons during that neonatal period remain unknown.

262 sms that govern regenerative capacity in the neonatal period remains a central goal in cardiac biolog

263 e, whereas in mice initially injected in the neonatal period, repeat administration resulted in high-

264 We show that the neonatal period represents a unique phase of thymic grow

265 ession during beta-cell development or early neonatal period resulted in severe glucose intolerance a

266 Inhibition of VEGF signaling during the neonatal period results in rapid loss of the dense capil

267 bout 65% of the expected number survived the neonatal period, revealing an important role for Blmh in

268 tions and strategies targeting the fetal and neonatal period should be prioritized for the prevention

269 aemorrhage and ventricular dilatation in the neonatal period showed the greatest decrease in CC area.

270 g spinal cord, following injuries during the neonatal period.SIGNIFICANCE STATEMENT Neonatal injury h

271 a critical response to the infection in the neonatal period that can lead to the failure of body org

272 tinal microbes and thymic lymphocytes in the neonatal period that can modulate host susceptibility to

273 at T4 and metformin, administered during the neonatal period that is equivalent to the third trimeste

274 In the neonatal period, the presence of circulating testosteron

275 takes (and the occurrence of MBD) during the neonatal period, the randomly assigned diets did not inf

276 were randomly assigned to a diet during the neonatal period; the diets used varied markedly in nutri

277 For children outside of the neonatal period, there appear to have been no respirator

278 During the neonatal period, these epigenetic changes and the reduct

279 gestive tract in pediatric patients from the neonatal period to adolescence.

280 cts and will need to be continued beyond the neonatal period to assess long-term pulmonary and neurod

281 t and which were not handled (NH) during the neonatal period underwent the same surgical procedures a

282 commensal bacteria is established during the neonatal period via regulatory T cells.

283 Infection in the neonatal period was also associated with impaired head g

284 Elevated blood lead concentration during the neonatal period was associated with higher PLAGL1/HYMAI

285 sty for native CoA during infancy beyond the neonatal period was examined in infants aged 3 to 12 mon

286 rtion of enteral intake as human milk in the neonatal period was inversely related to later mean arte

287 s in mice infected with H. pylori during the neonatal period was sufficient to break H. pylori-specif

288 h MBD are frequently asymptomatic during the neonatal period, we previously reported that MBD predict

289 Mutants that survived the neonatal period were hyperphagic, obese, diabetic, and i

290 o newborn infants by families throughout the neonatal period were recommended in intervention cluster

291 ncy virus (HIV)-infected children beyond the neonatal period were studied.

292 ion against malaria may have to begin in the neonatal period, when neonates have maternally acquired

293 The data revealed a neonatal period wherein T cells were not tolerant and in

294 ding 4.0 g/kg/day of amino acid early in the neonatal period while keeping the nitrogen to energy rat

295 Dmbx1 homozygous mutant mice died during the neonatal period, while others survived to adulthood; how

296 ants survived embryogenesis, but died in the neonatal period with malformations identical to the defe

297 21 SCID infants receiving transplants in the neonatal period with that in 70 SCID infants receiving t

298 itizing the host rat to similar cells in the neonatal period, without the need for additional immunos

299 2-dose vaccination schedule begun during the neonatal period would lead to, at most, a 7% increase in

300 To determine whether injection during the neonatal period would tolerize the host to the recombina