ライフサイエンスコーパス: healthy children

1 netic factors may underlie AVM in previously healthy children.

2 iated epileptic encephalopathy in previously healthy children.

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

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

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

6 externalizing behavior in a large sample of healthy children.

7 eferring affected children and overreferring healthy children.

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

9 ing HC overgrowth in contemporary samples of healthy children.

10 are unknown and difficult to investigate in healthy children.

11 endently contribute to higher systolic BP in healthy children.

12 chrony during visual attention compared with healthy children.

13 d frequency signatures of word processing in healthy children.

14 lculated from reference data obtained in 160 healthy children.

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

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

17 ry time with cardiometabolic risk factors in healthy children.

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

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

20 ared with cells from atopic nonasthmatic and healthy children.

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

22 amygdala activation than bipolar adults and healthy children.

23 that from cells from atopic nonasthmatic or healthy children.

24 han in cultures from atopic nonasthmatic and healthy children.

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

26 displayed reduced Efb cleavage compared with healthy children.

27 nd common spinal deformity seen in otherwise healthy children.

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

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

30 vely associated with cardiometabolic risk in healthy children.

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

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

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

34 disease in all cases, even among previously healthy children.

35 may significantly reduce the risk of MetS in healthy children.

36 that affects up to 3% of nonobese, otherwise healthy children.

37 r up to 80% of childhood stroke in otherwise healthy children.

38 ration of the booster dose of the vaccine in healthy children.

39 in life-threatening infections in previously healthy children.

40 ly expressed in SoJIA patients compared with healthy children.

41 rsity than populations in throat isolates of healthy children.

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

43 ren are often set above the requirements for healthy children.

44 (SLE), 6 patients with PAPA syndrome, and 39 healthy children.

45 ing functional magnetic resonance imaging in healthy children.

46 children with ADHD plus bipolar disorder and healthy children.

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

48 ors, who have significantly worse HRQOL than healthy children.

49 with formulas that have been established in healthy children.

50 ere never treated) and a control group of 59 healthy children.

51 ompared them to an age-matched cohort of 805 healthy children.

52 en with active or inactive juvenile DM or in healthy children.

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

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

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

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

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

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

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

60 normal elasticity values of the pancreas in healthy children.

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

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

63 educing the high incidence of fracture among healthy children.

64 ignificantly lower in allergic asthmatics vs healthy children.

65 which is otherwise correlated with aging in healthy children.

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

67 each hemisphere over the first 2 years in 32 healthy children, 14 children with unilateral stroke, an

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

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

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

71 o measure pupillary light reflex (PLR) in 44 healthy children (23 girls, 21 boys) from 6 to 16 years

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

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

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

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

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

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

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

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

80 Sixty-eight age-matched, developmentally healthy children acted as controls.

81 74, P = 0.03]: post hoc analyses showed, for healthy children, activation in both ventral and dorsal

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

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

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

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

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

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

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

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

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

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

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

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

94 lation between calcium intake and balance in healthy children aged 1-4 y consuming typical American d

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

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

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

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

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

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

103 1 month, and 1 year after the booster in 250 healthy children aged 6-12 years in an open-label phase

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

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

106 25(OH)D concentrations were measured in 382 healthy children aged 6-21 y living in the northeastern

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

108 A total of 601 healthy children (aged 1-10 years) were randomly selecte

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

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

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

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

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

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

115 Sixty healthy children and 20 healthy adults were studied usin

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

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

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

119 vaccine serotypes was 96% (95% CI 93-98) in healthy children and 81% (57-92) in those with coexistin

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

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

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

123 Numerous healthy children and adolescents are referred to pediatr

124 )D concentrations are prevalent in otherwise healthy children and adolescents in the northeastern Uni

125 Socially anxious and healthy children and adolescents learnt associations bet

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

127 239 healthy children and adolescents were genotyped and had

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

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

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

131 aks of severe invasive disease in previously healthy children and adults in the United States of Amer

132 nalyses generally showed that vaccination of healthy children and adults is cost-effective and is sen

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

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

135 Healthy children and adults without fever or illness ser

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

137 the effectiveness of vaccine, especially in healthy children and adults.

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

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

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

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

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

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

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

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

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

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

148 sh (80%), and 21 of 22 mothers who delivered healthy children and had no children with neonatal lupus

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

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

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

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

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

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

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

156 Healthy children and their mothers commonly harbor cipro

157 ever the discrepancy between developmentally healthy children and those with DS is greater for gratin

158 primary amebic meningoencephalitis (PAM) in healthy children and young adults.

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 d, 17 nasopharyngeal or throat isolates from healthy children, and 19 isolates from middle ear aspira

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 cortical and subcortical changes observed in healthy children, and contrast them with abnormal develo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

181 mples from 7 patients with juvenile DM and 7 healthy children, by real-time polymerase chain reaction

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

183 of A. actinomycetemcomitans in periodontally healthy children can serve as a risk marker for initiati

184 ith the Dietary Reference Intakes (DRIs) for healthy children, CF recommendations, and data from the

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

186 Healthy children conceived by ART display generalized va

187 s on the determinants of bone acquisition in healthy children conducted at this institution from 1992

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

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

190 CAMRSA colonization isolates collected from healthy children from Taipei who lacked MRSA risk factor

191 dren with uncomplicated malaria (UM), and in healthy children from the community, as control subjects

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

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

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

195 fluenzae (NTHi) to cause systemic disease in healthy children has been recognized only in the past de

196 Many healthy children have been born from eggs cryopreserved

197 Healthy children have wide variation in upper airway neu

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

199 ated with localized disease among previously healthy children; however, there are recent reports of m

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

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

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

203 varicella, the vaccine began to be tested in healthy children in Japan and elsewhere.

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

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

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

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

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

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

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

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

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

213 Sera from most healthy children less than 16 months old lacked NTS-spec

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

215 We studied, in otherwise healthy children < or =10 years old, HHV-7 and HHV-6 inf

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

217 reased RANKL:OPG ratio compared with that in healthy children (mean +/- SD 2.19 +/- 3.03 and 0.13 +/-

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

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

220 ed by the criterion 4-component model in 391 healthy children [mean (+/-SD) age, 11.7 +/- 4.2 y; 188

221 significant difference in serum NGAL between healthy children (median 80 ng/mL, interquartile ratio [

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

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

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

225 Clinically healthy children (n = 164) were enrolled in a placebo-co

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 of local WM growth rates in COS patients and healthy children over a 5-year period, based on analyzin

236 attention-deficit/hyperactivity disorder and healthy children (P < .05 corrected for multiple compari

237 15.7] vs 87.5 [SD, 13.6] for HIV-infected vs healthy children; P = .002).

238 ifficulties in psychosocial functioning than healthy children, particularly depression, anxiety and s

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

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

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

244 3 (95% confidence interval, 0.02-0.87) among healthy children reporting 6 doses of OPV, compared with

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

246 ndings, previously unrecognized in otherwise healthy children, suggest that HHV-7 viremia could repre

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

248 luenzae strains isolated from the throats of healthy children, suggesting that they may play a role i

249 hropometric equations that were derived from healthy children systematically overpredicted TBW and we

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

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

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

253 The authors conclude that in healthy children, the major explanatory variable for the

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 ctive juvenile DM, inactive juvenile DM, and healthy children were assessed for muscle strength (usin

263 ildren with diarrhea caused by rotavirus and healthy children were compared by using DNA microarray,

264 Fifteen healthy children were enrolled as controls.

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

266 nzae (NTHi) isolates from the throats of two healthy children were genotyped by multilocus sequence t

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

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

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

270 One hundred healthy children were recruited prospectively and consec

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

272 stemic-onset disease), 100 JRA ASPs, and 688 healthy children were tested for anti-CCP antibodies and

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

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

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

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

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

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

279 Most fecal samples from healthy children who received OPV were found to contain

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

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

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

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

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

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

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

287 Additional investigations in healthy children with a known history of malaria showed

288 Among healthy children with a single anesthesia exposure befor

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

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

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

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

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

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

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

296 In otherwise healthy children without chronic complicating factors su

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

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

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

300 In otherwise healthy children younger than three years of age who hav