ライフサイエンスコーパス: healthy children

1 Low levels of HMPV are rarely detected in healthy children.

2 o compare the results obtained with those in healthy children.

3 s in children but are often detected also in healthy children.

4 pression was similar in children with AD and healthy children.

5 adjuvanted TIV (ATIV) in 90 14- to 24-mo-old healthy children.

6 s in the metabolic spectrum in the brains of healthy children.

7 ty of RSV disease severity, especially among healthy children.

8 tients as a surrogate to normative data from healthy children.

9 educing the high incidence of fracture among healthy children.

10 ignificantly lower in allergic asthmatics vs healthy children.

11 which is otherwise correlated with aging in healthy children.

12 iated epileptic encephalopathy in previously healthy children.

13 hildren with AOM and 235 throat strains from healthy children.

14 nize the tonsils and pharynx of up to 20% of healthy children.

15 externalizing behavior in a large sample of healthy children.

16 pendently influence autonomous behaviours in healthy children.

17 eferring affected children and overreferring healthy children.

18 ot suspected of having an infection), and 40 healthy children.

19 ing HC overgrowth in contemporary samples of healthy children.

20 are unknown and difficult to investigate in healthy children.

21 endently contribute to higher systolic BP in healthy children.

22 d frequency signatures of word processing in healthy children.

23 lculated from reference data obtained in 160 healthy children.

24 of TSLP after RSV infection than cells from healthy children.

25 in the HPRT locus in peripheral T cells from healthy children.

26 ry time with cardiometabolic risk factors in healthy children.

27 onset depression (PO-MDD) in comparison with healthy children.

28 en than in cells from atopic nonasthmatic or healthy children.

29 ared with cells from atopic nonasthmatic and healthy children.

30 amygdala activation than bipolar adults and healthy children.

31 that from cells from atopic nonasthmatic or healthy children.

32 han in cultures from atopic nonasthmatic and healthy children.

33 displayed reduced Efb cleavage compared with healthy children.

34 nd common spinal deformity seen in otherwise healthy children.

35 itis media than in those from the throats of healthy children.

36 d comparable to vaccine-induced responses of healthy children.

37 d to be the most reliable frequency bands in healthy children.

38 ng the children with IE with a cohort of 847 healthy children.

39 ssing results about the mechanisms of VPL in healthy children.

40 to the live attenuated SA 14-14-2 vaccine in healthy children.

41 re reduced in critical illness compared with healthy children.

42 lic profiles in critically ill compared with healthy children.

43 to the live-attenuated SA 14-14-2 vaccine in healthy children.

44 ithin paedatric brain tumor survivors versus healthy children.

45 malnourished children than among age-matched healthy children.

46 normal elasticity values of the pancreas in healthy children.

47 l bacteria at 12 months of age compared with healthy children.

48 netic factors may underlie AVM in previously healthy children.

49 c DNA is frequently detected in both ill and healthy children.

50 66 eBL patients, 78 non-eBL cancers, and 202 healthy children.

51 chrony during visual attention compared with healthy children.

52 fected AD skin than from the nasal cavity of healthy children.

53 M, and the control group was comprised of 60 healthy children.

54 vely associated with cardiometabolic risk in healthy children.

55 I), and elasticity values of the pancreas in healthy children.

56 in life-threatening infections in previously healthy children.

57 est patient having function close to that in healthy children.

58 asthma without obstruction, or in BECs from healthy children.

59 From December 2008 to June 2011, healthy children 1 to 5 years of age were recruited duri

60 rvivors [11.81 +/- 3.27)] and 24 age matched healthy children [12.04 +/- 3.28)] in functional connect

61 a brain tumor (12.67 +/- 2.76 years), and 26 healthy children (16/10: male/female; 12.01 +/- 3.9 year

62 ildren with therapy-resistant asthma than in healthy children (19.2 ng/mL vs 13.8 ng/mL, P = .03).

63 virologically confirmed dengue (VCD) in 3424 healthy children, 2 to 16 years of age, in Asia (Indones

64 -18 years of age, divided into 3 groups: 165 healthy children, 29 children with IHT (all >4 years of

65 Participants included healthy children 3 to 6 years old (vaccinated with the 1

66 Healthy children (3-18 years old) and adults, and indivi

67 The right eyes from 110 healthy children, 3-6 years of age, were scanned with th

68 A total of 181 eyes of 92 healthy children (39 girls, 53 boys) aged 6.5 and servin

69 re prevalent in eBL patients (74.5%) than in healthy children (47.5%) (odds ratio = 3.24, 95% confide

70 the Expanded Program on Immunization [EPI]), healthy children 5 to 10 years old (age-ineligible for P

71 In the reference population of 51,332 healthy children, 5 age-specific and sex-specific growth

72 Asthmatic and healthy children (6-17 years) were enrolled in the study

73 Two hundred ninety-seven healthy children (6-18 years; mean = 12 +/- 3 years), wi

74 Twenty healthy children (8 boys), with an age range of 4-14 yea

75 We retrospectively recruited 198 otherwise healthy children (93% White) hospitalized for severe RSV

76 s exist in spirometric pulmonary function in healthy children across the Indian urban-rural continuum

77 74, P = 0.03]: post hoc analyses showed, for healthy children, activation in both ventral and dorsal

78 d Glu/H2O levels were acquired in a group of healthy children, adolescents, and adults in a subcortic

79 ening infectious diseases striking otherwise healthy children, adolescents, and even young adults hav

80 Among 2014 healthy children, adolescents, and young adults (1022 [5

81 derived measures of brain development in 628 healthy children, adolescents, and young adults in the l

82 Participants were healthy children, adolescents, and young adults.

83 We genotyped 714 healthy children after 2 age-appropriate doses of rubell

84 rm effects on pulmonary health in previously healthy children after acute respiratory failure requiri

85 e encephalopathy that can occur in otherwise healthy children after common viral infections such as i

86 nicipality, 13 family pediatricians enrolled healthy children (age range, 2.0-5.8 years) in the study

87 ased, prospective study including previously healthy children aged >=28 days and <17 years admitted w

88 ty and disease severity of IPD in previously healthy children aged <5 years.

89 In this cross-sectional study, we enrolled healthy children aged 0-23 months who lived within the s

90 -based three-arm cluster randomised trial in healthy children aged 1 month to 5 years that resided wi

91 ls consisted of muscle biopsy specimens from healthy children aged 1 to 3 years who had undergone ana

92 Among healthy children aged 1 to 5 years, daily administration

93 observational and interventional studies of healthy children aged 1-18 y that described the associat

94 nd clustered cardiometabolic risk factors in healthy children aged 10 y.We included 700 children (49.

95 Healthy children aged 12-22 months were randomised (3:3:

96 The participants were otherwise healthy children aged 2 to 17 years with moderate to sev

97 n meters squared) z score in a cohort of 226 healthy children aged 2 to 6 years attending day care at

98 Between June 3, and Dec 1, 2011, healthy children aged 2-14 years were randomly assigned

99 ght, and height were measured in 1122 normal healthy children aged 2-21 y.

100 trial done near Niakhar, Senegal, generally healthy children aged 2-5 years were randomly allocated

101 e (QIV) containing both B lineages vs TIV in healthy children aged 3-17 years.

102 Healthy children aged 4-16 years were randomly assigned

103 ated tetravalent dengue vaccine (TAK-003) in healthy children aged 4-16 years.

104 vaccines (NCT01051661), RSV epidemiology in healthy children aged 6 months to <10 years at first vac

105 ational cross-sectional study recruiting 113 healthy children aged 6 to 17 years with no ocular abnor

106 1 month, and 1 year after the booster in 250 healthy children aged 6-12 years in an open-label phase

107 MATERIAL/METHODS: Forty-nine healthy children aged 6-15 years (mean 11.6 years) were

108 Sixty healthy children aged 6-17 years were studied with a who

109 a prospective echocardiographic study in 756 healthy children (aged 1 day to 18 years) and in 54 chil

110 This institutional study enrolled 83 healthy children (aged 5-15 years) as volunteer research

111 neurocognitive testing was performed in 408 healthy children (aged 6, 18, and 24 mo) from uncomplica

112 Among healthy children ages 9 months to 16 years (n = 165), th

113 Forty-eight healthy children (ages 5.8 to 15.8 years) underwent opti

114 ith IBS (pediatric Rome III criteria) and 22 healthy children, ages 7-12 years, by 16S ribosomal RNA

115 Growth monitoring of apparently healthy children aims at early detection of serious unde

116 eral blood mononuclear cells (PBMCs) from 59 healthy children and 136 patients with JIA (28 with enth

117 Sixty healthy children and 20 healthy adults were studied usin

118 ime tasks of varying cognitive loads from 18 healthy children and 20 patients.

119 IgG Fc glycans were characterized in 225 healthy children and 40 children with unexplained recurr

120 ripheral blood samples were obtained from 59 healthy children and 61 children with polyarticular JIA

121 ing lower airway plugs were obtained from 10 healthy children and 8 children with asthma.

122 were measured in 24-h urine samples from 524 healthy children and adolescents (aged 6-17 y) participa

123 rences in a large and well matched sample of healthy children and adolescents (n = 190) aged 5-18 yea

124 Healthy children and adolescents 4 to 16 years of age we

125 in a longitudinal sample of developmentally healthy children and adolescents 4-22 years old.

126 In a sample of 92 healthy children and adolescents aged 8-19 years, we aim

127 Numerous healthy children and adolescents are referred to pediatr

128 Socially anxious and healthy children and adolescents learnt associations bet

129 g in the somatosensory system (somato-SG) in healthy children and adolescents using magnetoencephalog

130 s and life-threatening illness in previously healthy children and adolescents.

131 In Mali, 251 healthy children and adults aged 4-25 years who were fre

132 cipants across a spectrum of symptomatic and healthy children and adults by utilizing both germline a

133 The cohort encompassed healthy children and adults from the Amazonas of Venezue

134 valent dengue vaccine candidate (TAK-003) in healthy children and adults living in dengue-endemic are

135 All healthy children and adults tested could learn the new t

136 We studied 5 previously healthy children and adults with unexplained invasive di

137 communities of primary clinical samples from healthy children and adults, based on sequencing of a fu

138 nasal filters and washes from a group of 40 healthy children and adults.

139 agnosed from 1963 through 1973, in otherwise healthy children and alive at 15 years of age.

140 In a study involving healthy children and asthmatics, a polymorphism in the 3

141 VDPVs isolated from the patients and from 12 healthy children and characterized phenotypic aspects, i

142 of temporal changes in the serum proteome in healthy children and children progressing to type 1 diab

143 s IgA recognition patterns, differed between healthy children and children with allergic manifestatio

144 Air-liquid interface cultures from healthy children and children with asthma were also test

145 lmonary exercise testing is feasible in both healthy children and children with cardiac disease.

146 n with inflammatory and clinical features in healthy children and children with difficult-to-treat as

147 IgG glycans from healthy children and disease-modifying antirheumatic dru

148 ract caused by Candida species in previously healthy children and even adults might be caused by inhe

149 ics of calcium absorption and utilization in healthy children and in children with chronic diseases.

150 e 6E, and they were recovered worldwide from healthy children and patients of all ages with pneumococ

151 e first large-scale survey of IgG glycans in healthy children and patients with JIA, with a focus on

152 hereditary periodic fevers (HPFs), and from healthy children and pediatric HPF patients.

153 The intestinal microbiomes of healthy children and pediatric patients with irritable b

154 Severe influenza disease strikes otherwise healthy children and remains unexplained.

155 ganism causes cervicofacial lymphadenitis in healthy children and severe disease in immunocompromised

156 lciparum parasitemia is common in apparently healthy children and severe malaria is commonly misdiagn

157 Healthy children and their mothers commonly harbor cipro

158 nificant differences in between the ONSDs of healthy children and those in subjects with ODD.

159 disordered breathing (SDB) is different from healthy children and, if so, whether it resolves with tr

160 WMHs are rare in healthy children and, when observed, often occur with co

161 with new-onset CD, 45 treated with a GFD, 57 healthy children, and 19 unaffected siblings of children

162 severe, therapy-resistant asthma compared to healthy children, and also compared to children with con

163 the characteristics of DC in the airways of healthy children, and children with asthma, are currentl

164 dren with active vasculitis as compared with healthy children, and the levels declined with remission

165 Cross-sectional studies, studies of healthy children, and those without defined criteria for

166 ildren with EoE is (i) distinct from that of healthy children; and (ii) different from that of adults

167 Studies reviewed GE in both healthy children as well as those with neurodevelopmenta

168 were related to the neurologic condition of healthy children at 18 mo of age: children with minimal

169 Uncomplicated encounters included healthy children at initial presentation of illness.

170 Upper respiratory microbiota profiles of 60 healthy children at the ages of 1.5, 6, 12, and 24 month

171 Children with EoE can be distinguished from healthy children based on the molecular patterns of thei

172 CT, normative RNFL and macular parameters in healthy children below 18 years of age were established;

173 t reported heart rate or respiratory rate of healthy children between birth and 18 years of age.

174 here dengue is endemic, we randomly assigned healthy children between the ages of 9 and 16 years in a

175 er echocardiography) vascular function in 65 healthy children born after ART and 57 control children.

176 Healthy children born at term were enrolled in the Infan

177 The analysis included 38,055 otherwise healthy children born prematurely who were enrolled for

178 Although shorter than healthy children, boys with CF were heavier and had a BC

179 Venous thromboembolism (VTE) is rare in healthy children, but is an increasing problem in childr

180 asons to limit antibiotic exposure in young, healthy children, but weight gain is likely not one of t

181 hildren with mild and severe RSV disease and healthy children by 16S-rRNA sequencing.

182 Information obtained from healthy children can serve as a baseline against which p

183 analysis of wheat and rice sIgG and sIgG4 in healthy children, children with IgE-mediated wheat aller

184 Healthy children conceived by ART display generalized va

185 of vitamin A supplementation at the RDA for healthy children did not improve serum retinol values in

186 f the macular ganglion cell complex (GCC) in healthy children facilitates interpretation of OCT data.

187 In healthy children food sIgG were the lowest; no sIgG4 wer

188 ed from adenotonsillectomy waitlists, and 20 healthy children from the community underwent overnight

189 ise description of microbiota development in healthy children from this and other low-income countrie

190 flexibility and brain gray matter density in healthy children from two birth cohorts-MAVAN from Canad

191 sing prospective longitudinal populations of healthy children from two North American populations, we

192 First, 51 healthy children (from neonate to 15 years) were analyze

193 ed with normal growth and development (i.e., healthy children) from the progression of CF lung diseas

194 Many healthy children have been born from eggs cryopreserved

195 malaria (SM; age range, 4 to 9 years) and 7 healthy children (HC; age range, 4 to 8 years) to measur

196 erebral falciparum malaria (CM; n = 45), and healthy children (HC; n = 109).

197 Compared with HDL from healthy children, HDL(CKD) strongly inhibited nitric oxi

198 Mortality rates in previously healthy children hospitalized with RSV are <0.5%, but up

199 We tested serum samples from 148 healthy children immunized against varicella in New York

200 ator A, to discriminate between IDA, TT, and healthy children in a Chinese population.

201 between children with controlled asthma and healthy children in any of the end points.

202 and family functioning domains compared with healthy children in later months.

203 Healthy children in one of three age groups (24-59 month

204 Both AFP patients and healthy children in Pakistan were found to be excreting

205 However, the frequency among healthy children in the community is not well characteri

206 SNPs and brain structural connectomes in 678 healthy children in the PING study.

207 autism spectrum disorder in three previously healthy children in the second year of life.

208 Nine hundred healthy children in Vellore, India, aged 1-4 years were

209 skewed toward proinflammatory G0 variants in healthy children, in particular during the first few yea

210 ssociation of 11betaHSD2 activity with BP in healthy children independent of known BP-related dietary

211 ared with cells from atopic nonasthmatic and healthy children intrinsically or in response to IL-4/IL

212 Data suggest that, relative to healthy children, irritable children have deficient rewa

213 tory afebrile form of seizures in previously healthy children is being increasingly recognized in aro

214 ng the development of the oral microbiota in healthy children is of great importance to oral and gene

215 d associated cardiometabolic risk factors in healthy children is unknown.

216 elops in up to potentially 44% of previously healthy children less than or equal to 24 months old at

217 amples and 27 fecal samples from age-matched healthy children living in the same area.

218 has been linked to reduced lung function in healthy children, longitudinal analyses of pollution eff

219 gnetic signatures of language development in healthy children may be used as references for future id

220 children with CF (mean age, 1.55 yr) and 25 healthy children (mean age, 1.26 yr) underwent multiple-

221 nctional MRI to measure brain activity in 24 healthy children (mean age, 10.2 y) while they attended

222 lls/L; 83% with undetectable HIV RNA) and 37 healthy children (median age, 12.1 years) were included.

223 tors for a classifier that could distinguish healthy children, mild-to-moderate allergic asthmatics,

224 children with controlled asthma (n = 57) and healthy children (n = 14), especially before the adminis

225 PBMCs were collected from healthy children (n = 16) and children with asthma (n =

226 ldren with AD (n = 56) compared to nonatopic healthy children (n = 25).

227 We studied healthy children (n = 48, 4-12 years, 24 females) and ch

228 ldren with renal failure (n=80) with that in healthy children (n=20) using multiparameter flow cytome

229 astating condition that occurs in previously healthy children of all ages and frequently leads to a r

230 NV) study on 1,013 cases with ADHD and 4,105 healthy children of European ancestry using 550,000 SNPs

231 study on a cohort of 859 ASD cases and 1,409 healthy children of European ancestry who were genotyped

232 ) of a child's faecal microbiota relative to healthy children of similar chronologic age.

233 is strains, isolated from the nasopharynx of healthy children or middle ear effusions from patients w

234 r population of cells is found abundantly in healthy children, or in patients with pancreatitis or T1

235 different from that in samples obtained from healthy children (P<0.001 by permutational multivariate

236 15.7] vs 87.5 [SD, 13.6] for HIV-infected vs healthy children; P = .002).

237 We investigated PeV epidemiology in healthy children participating in a community-based, lon

238 Overall, compared with healthy children, patients showed the following: (1) low

239 Compared to healthy children, pediatric brain tumor survivors show i

240 centile ranges for midupper arm measures for healthy children provide a useful nutritional assessment

241 ptibility to severe VZV disease in otherwise healthy children, providing evidence for an essential ro

242 Healthy children received a single, intranasal dose of L

243 A total of 20,869 healthy children received either vaccine or placebo.

244 n age-matched, sex-matched, and time-matched healthy children recruited from the community.

245 The hedonic response of 104 healthy children, recruited from day-care centres and sc

246 3 (95% confidence interval, 0.02-0.87) among healthy children reporting 6 doses of OPV, compared with

247 l genetic cause, we recruited 120 previously healthy children requiring support in intensive care bec

248 e population-based cohort study, we enrolled healthy children residing in Bogo or Balamban, Cebu, Phi

249 OCT measurements of GCC in healthy children show excellent reproducibility.

250 as associated with height in a cohort of 227 healthy children, suggesting that HOXA4 may play a role

251 dy that included longitudinal growth data of healthy children (the reference population) from primary

252 We found that in healthy children, the adolescent growth spurt is standar

253 may be adequate for testing among otherwise healthy children, the decreased sensitivity may be probl

254 Patients in these reports included otherwise healthy children, those with inflammatory bowel disease

255 of three different tonometers on a group of healthy children to see whether differences exist and wh

256 ge:13+/-2) with WS and 15 age/gender-matched healthy children using a manual region-of-interest analy

257 ed, large cohorts-440 healthy adults and 662 healthy children-using high-resolution structural neuroi

258 The mean (SD) LCI in healthy children was 6.45 (0.49).

259 ut bacterial communities of NASH, obese, and healthy children was determined by 16S ribosomal RNA pyr

260 solated from the stool samples of apparently healthy children was investigated in mice and rats.

261 ATEMENT By comparing brain tumor patients to healthy children, we establish that changes in the micro

262 Escherichia coli from Shigella-infected and healthy children, we identified an extensive array of AM

263 tween patients on a GFD with new-onset CD vs healthy children were associated with nutrient and food

264 Fifteen healthy children were enrolled as controls.

265 Healthy children were followed up as controls (n = 143).

266 y exacerbations, whereas similar symptoms in healthy children were not associated with increased LCI

267 h an acute febrile infectious disease and 30 healthy children were obtained as control.

268 A total of 151 healthy children were randomized 1:1 to receive the vacc

269 One hundred healthy children were recruited prospectively and consec

270 Three hundred and fifty-seven healthy children were recruited.

271 ng pulsed-wave tissue Doppler imaging in 380 healthy children were used to transform patient data int

272 umococcal serotypes most commonly carried by healthy children, whereas S-OM was associated with serot

273 nd Lautropia mirabilis were most abundant in healthy children, while Aa, Fa, Tannerella sp, Solobacte

274 system or the lungs in unrelated, otherwise healthy children who are heterozygous for rare missense

275 (GA1) between 1989 and 1993, we found three healthy children who excreted abnormal quantities of glu

276 However, two-thirds of healthy children who excreted this virus reported >or=6

277 Medical records of healthy children who received strabismus surgery for acc

278 s found in saliva derived from periodontally healthy children who subsequently developed alveolar bon

279 s cross-sectional trial was performed in 147 healthy children who underwent transabdominal ultrasonog

280 Healthy children who were attending Our Lady's Children'

281 Of 38,055 otherwise healthy children who were born prematurely, 583 received

282 virus in stool samples obtained from 14,005 healthy children who were in contact with 2761 individua

283 ikely to be nonsecretors (13%) compared with healthy children who were not of Hispanic ethnicity (25%

284 We also studied 13 healthy children whose age ranges overlapped those of th

285 Among healthy children with a single anesthesia exposure befor

286 econsider the practice of treating otherwise healthy children with acute osteomyelitis with prolonged

287 morbidity in a population of only previously healthy children with acute respiratory failure.

288 Healthy children with available day-0 sera, a complete f

289 S to a population-based cohort of previously healthy children with bacterial sepsis detected variants

290 ECENT FINDINGS: Routine airway management in healthy children with normal airways is simple in experi

291 We enrolled previously healthy children with RSV infection.

292 A total of 282 healthy children with serial scans were included as cont

293 lling AHA criteria; and group III, otherwise healthy children with some KD-like features ultimately d

294 olvement, has been described increasingly in healthy children with the spread of community-associated

295 psychological stress and immune response in healthy children, with special focus on autoimmunity.

296 ort, CA-CDI is more often seen in previously healthy children without antibiotic exposure or comorbid

297 ed children with asthma (n = 18) and matched healthy children without asthma (n = 8) were differentia

298 CL8/CXCL11), we screened 92 asthmatic and 69 healthy children without illness for respiratory virus i

299 from the Congo with konzo and 87 presumably healthy children without konzo from neighbouring househo

300 Previously healthy children younger than 2 years old (n = 151) were