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 we observed a very beneficial effect in the neonatal period.

3 for infants with severe infection during the neonatal period.

4 velopment of in vivo cytotoxicity during the neonatal period.

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

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

7 cessive diarrheal disorder presenting in the neonatal period.

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

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

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

11 tensive care or factors operating beyond the neonatal period.

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

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

14 y skewed inactivation, especially during the neonatal period.

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

16 s serious morbidity and mortality during the neonatal period.

17 stage-dependent manner permissive during the neonatal period.

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

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

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

21 %) of double-homozygous mice died during the neonatal period.

22 irculating levels of sex steroids during the neonatal period.

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

24 permeability barrier maturation in the early neonatal period.

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

26 nvariably fatal course when diagnosed in the neonatal period.

27 N370S homozygosity was lethal in the neonatal period.

28 in rapidly growing normal tissues during the neonatal period.

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

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

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

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

33 result of priming of splenocytes within the neonatal period.

34 r cystic periventricular leukomalacia in the neonatal period.

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

36 ndition that afflicts preterm infants in the neonatal period.

37 pment of the somatosensory cortex during the neonatal period.

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

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

40 ost common gastrointestinal emergency in the neonatal period.

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

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

43 bacterium that causes meningitis during the neonatal period.

44 A further nine died within the neonatal period.

45 c levels of circulating FVIII throughout the neonatal period.

46 This advantage largely disappeared after the neonatal period.

47 nd require constant attention throughout the neonatal period.

48 supranormal levels of FVIII activity in the neonatal period.

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

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

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

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

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

54 orpuscles after nerve resection in the early neonatal period.

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

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

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

58 ment in shaping cortical activity during the neonatal period.

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

60 patients with respiratory failure beyond the neonatal period.

61 or duration of sleep impairments beyond the neonatal period.

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

63 s disorders of gastrointestinal tract during neonatal period.

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

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

66 cuate nucleus of the hypothalamus during the neonatal period.

67 d extensive in situ proliferation during the neonatal period.

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

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

70 icy of transatrial repair delayed beyond the neonatal period.

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

72 with both characteristics extend beyond the neonatal period.

73 sopressors and blood transfusions during the neonatal period.

74 orn premature and required intubation during neonatal period.

75 caused by pulmonary hypoplasia in the early neonatal period.

76 rom white matter injury sustained during the neonatal period.

77 the clinical approach to neutropenia in the neonatal period.

78 on thymic development may extend beyond the neonatal period.

79 icrobiome to dietary substrates in the early neonatal period.

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

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

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

83 equence of pulmonary inflammation during the neonatal period.

84 t optimizing successful breastfeeding in the neonatal period.

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

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

87 eart regeneration, particularly in fetal and neonatal periods.

88 d autonomic ganglia during the embryonic and neonatal periods.

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

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

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

92 21 SCID infants with transplantations in the neonatal period, 20 (95%) survive.

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

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

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

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

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

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

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

100 38% (MRR, 0.62; 95% CI, .46-.83) within the neonatal period and 16% (0.84; .71-1.00) by age 12 month

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

102 ; 80 in control clusters), 77 died after the neonatal period and before 18 months (31 in intervention

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

146 During the neonatal period, calcitriol-stimulated intestinal calciu

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

191 The neonatal period is crucial for the early microbial colon

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

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

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

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

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

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

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

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

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

201 The neonatal period marks an important time in mammalian imm

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

227 In the neonatal period, the presence of circulating testosteron

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

246 21 SCID infants receiving transplants in the neonatal period with that in 70 SCID infants receiving t

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

248 2-dose vaccination schedule begun during the neonatal period would lead to, at most, a 7% increase in

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