ライフサイエンスコーパス: early intervention

1 fy high-risk women who should be targets for early intervention.

2 identify a high-risk subset of survivors for early intervention.

3 g brain markers might assist in referral for early intervention.

4 on for informing treatment approaches during early intervention.

5 mer's disease is important for prognosis and early intervention.

6 on and could benefit from clinical trials of early intervention.

7 h AVD by promoting personalized medicine and early intervention.

8 s cause long-term morbidity but benefit from early intervention.

9 mental, and early detection is essential for early intervention.

10 t redox modulation as a potential target for early intervention.

11 oups and geographic location for focused and early intervention.

12 the overall health of the infant assists in early intervention.

13 s that can further reduce infarct size after early intervention.

14 used public health target for prevention and early intervention.

15 y progress to invasiveness in the absence of early intervention.

16 ant insight into the etiology of obesity and early intervention.

17 tify high-risk patients who may benefit from early intervention.

18 follow individuals at risk for HCC, enabling early intervention.

19 n adolescence has important implications for early intervention.

20 fessionals who may provide prevention and/or early intervention.

21 those at risk is essential to any vision of early intervention.

22 sk of mesothelioma who could be targeted for early intervention.

23 tive systems, underscoring the importance of early intervention.

24 ing to cognitive impairment and a target for early intervention.

25 indow of opportunity for chemoprevention and early intervention.

26 eatment, the condition is fatal and requires early intervention.

27 albeit to a lesser extent than observed with early intervention.

28 cations for designing rational approaches to early intervention.

29 stage disease, offering the opportunity for early intervention.

30 tanding PsAF, underscoring the importance of early intervention.

31 control based on therapeutic monitoring and early intervention.

32 achexia in cancer patients are necessary for early intervention.

33 but also providing potential strategies for early intervention.

34 ritical step toward advancing prevention and early intervention.

35 d to detect behavioural changes relevant for early intervention.

36 viduals at highest risk who may benefit from early intervention.

37 t may precede systemic infection and require early intervention.

38 dict risk and aid in stratification to guide early interventions.

39 litate early diagnosis and access to crucial early interventions.

40 disease have nurtured the emergent need for early interventions.

41 may inform the construction of more targeted early interventions.

42 risk for later major depression and applying early interventions.

43 sible and neurodegeneration preventable with early interventions.

44 in recent trauma survivors is important for early interventions.

45 h should look at this interplay for possible early interventions.

46 in an independent testing set, facilitating early interventions.

47 nhibitor (GS-444217 delivered in chow) as an early intervention (2-8 weeks after STZ) or late interve

48 avioral impairment, were examined under both early intervention (7-month-old young-adult male mice wi

49 ification-tree algorithm to guide studies of early intervention after CAR T-cell infusion for patient

50 This study tested an early intervention aimed at modifying the memory to prev

51 Early interventions aimed at altering rejection-like inf

52 risk for ASD who might benefit from targeted early interventions aimed at preventing or ameliorating

53 The early intervention also normalized brain function, enhan

54 Early intervention among those involved in bullying can

55 size would provide a greater opportunity for early intervention and family counseling as well as furn

56 rguments in favor of NBS include benefits of early intervention and follow-up for the identified baby

57 Research must inform the benefits of early intervention and implementation of policies to add

58 apidly detectable AKI biomarkers could allow early intervention and improve outcomes.

59 eath, and they may provide opportunities for early intervention and improved survival after hematopoi

60 ead to new insight for developing biomarker, early intervention and novel therapeutics.

61 sceptibility is warranted to inform targeted early intervention and prevention efforts.

62 Early intervention and prevention of psychosis remain a

63 sed interest in exploring the possibility of early intervention and prevention trials, targeting MCI

64 d that prevention of recurrences may require early intervention and restricted use of antidepressants

65 s may allow an improvement in monitoring and early intervention and so prevent early graft loss.

66 rricular approaches can serve as a model for early intervention and special education programs.

67 lculator represents a meaningful step toward early intervention and the personalized treatment of psy

68 Early intervention and tight control of inflammation opt

69 s desirable, the evidence of the benefits of early intervention and treatment for older hospitalised

70 en increasing attention to the importance of early intervention and whether treatment effects may be

71 ight be incorporated into newborn screening, early intervention and, perhaps, carrier testing and pre

72 gh risk of AD would be important in planning early intervention and/or prevention studies.

73 of natural disasters should be targeted with early interventions and active long-term follow-up to pr

74 The effects of early interventions and longer term implications of thes

75 n of those parents at high risk and for more early interventions and prevention research, especially

76 nisms, improve strategies for prevention and early intervention, and better target our treatments thr

77 vel strategies for the diagnosis, treatment, early intervention, and prevention of schizophrenia.

78 require improved public health, prevention, early intervention, and treatment activities.

79 Proponents of early intervention argue that the complications of CLM,

80 The early intervention arm subjects detected exacerbations m

81 The early intervention arm subjects measured home spirometry

82 osclerosis, and second cancer in MPNs favors early intervention at the time of diagnosis (statins and

83 early biomarkers and new targets to promote early intervention beginning in school age.

84 mly assigned to receive three sessions of an early intervention beginning in the emergency department

85 hat required penetrating keratoplasty was an early intervention believed to be a direct sequelae of t

86 cognitive deficits late in life, suggesting early intervention by enhancing GABA signaling as a pote

87 and outcome, we examined the effects of very early intervention by injecting NDM mice with high-dose

88 However, early intervention can achieve better rescue.

89 en who are at high risk for deficits so that early intervention can be initiated to mitigate the impa

90 It is not known whether early intervention can improve long-term autism symptom

91 Whether early intervention can prevent development of ARDS remai

92 Participants were recruited from early intervention centers.

93 res are needed for diagnostic monitoring and early intervention clinical trials.

94 ical monitoring, risk factor evaluation, and early intervention could benefit women with hypertension

95 sk family members for clinical screening and early intervention could reduce morbidity and mortality.

96 ill discover biomarkers that may help in the early intervention, diagnosis or treatment of SZ.

97 is, supporting their potential utility as an early intervention during pulmonary infections.

98 Here, we tested the hypothesis that this early intervention effect is modulated by the context of

99 may be a potential target for prevention and early intervention efforts aimed at reducing the occurre

100 ng patients who receive TBI may benefit from early intervention efforts to minimize cognitive losses

101 omising public health strategy for providing early intervention for a variety of child mental health

102 active B-type natriuretic peptide (iBNP) and early intervention for acutely decompensated heart failu

103 , medical management and decisions regarding early intervention for aortic disease.

104 Focused early intervention for communication during mechanical v

105 nt paradigms, with the possible inclusion of early intervention for contracture avoidance and assista

106 nts experiencing CAR T-cell toxicities, with early intervention for hypotension and treatment of conc

107 Web-based psychoeducation and targeted brief early intervention for injured children and their parent

108 Early intervention for neglect or emotional abuse in pre

109 ive biomarker to enable close monitoring and early intervention for patients receiving ipilimumab.

110 Early intervention for substance use is critical to impr

111 guage, the results point to the necessity of early intervention for the individuals with autism who s

112 ity model reveals the critical importance of early intervention for the prevention of subsequent allo

113 ctable physical obstruction, suggesting that early intervention for this disease may prevent more irr

114 individuals with SCA is warranted, enabling early intervention for those at risk.

115 ed controlled trial (RCT) of a comprehensive early intervention for toddlers with ASD demonstrated ga

116 group support can offer a clinically useful early intervention for weight management in overweight a

117 Early interventions for at-risk ICU survivors may improv

118 orn or infant screening as a way of ensuring early interventions for FXS.

119 Prevention of and early interventions for psychiatric illness and treatmen

120 Results of small trials suggest that early interventions for social communication are effecti

121 ional studies have the potential to optimize early interventions for the therapy of chronic addictive

122 antisocial personality were improved in the early intervention group at long-term follow-up compared

123 The early intervention group received early cuff deflation a

124 evidence on the effectiveness of prevention, early intervention, harm reduction, and treatment of pro

125 Although early intervention has been shown to support more normat

126 Family-centered early intervention has the potential to prevent problems

127 Although early interventions have been used for the treatment of

128 We find that the best control strategy is early intervention heavily based on prophylaxis at a lev

129 ism has heavily emphasized the importance of early intervention (i.e. treatment before the age of 4 y

130 This is disconcerting because early intervention improves outcomes and deterioration i

131 Early intervention improves prognosis in autism spectrum

132 sing celiac disease will lead to appropriate early intervention in affected children RECENT FINDINGS:

133 Early intervention in Alzheimer's Disease (AD) requires

134 practices for a genetics-driven approach to early intervention in at-risk relatives.

135 ction after a randomised controlled trial of early intervention in autism spectrum disorder.

136 utic target in the Wnt signaling pathway for early intervention in CCT.

137 First is a re-examination of strategies for early intervention in critical aortic stenosis.

138 An optimal therapeutic candidate for early intervention in ischemic stroke should be effectiv

139 Early intervention in offspring of 2 generations affecte

140 atments may provide the basis for aggressive early intervention in patients with MS and intensificati

141 study provides evidence for the efficacy of early intervention in preventing adult psychopathology a

142 erging data pointing to the effectiveness of early intervention in remediating neurodevelopmental con

143 Early intervention in select patients may lead to potent

144 and functional remodelling, suggesting that early intervention in the insulin-adrenergic signalling

145 The limitations and caveats of early interventions in psychiatric disorders are also di

146 e adopted in practice to guide postdischarge early interventions, including the integrated provision

147 eriod for the onset of eating disorders, and early intervention is critical.

148 Early intervention is crucial for the prevention of diab

149 BP is associated with BP in later life, and early intervention is important.

150 Early intervention is necessary to minimize morbidities

151 Early intervention is needed to reduce the risk of endom

152 Early intervention likely prevented morbidity and possib

153 Early intervention may be key to safe and effective ther

154 Furthermore, early intervention may prevent long-term deficits in mem

155 ogical screening of vulnerable survivors and early intervention may prevent the onset and/or reduce t

156 l of disease reversibility and suggests that early intervention might be beneficial for FXTAS patient

157 Early intervention might improve long-term outcomes for

158 in this population and to establish whether early intervention might slow this disease progression.

159 ratios could be used for identification and early intervention of at-risk obese individuals.

160 onstitute the first assessment of mNPC as an early intervention on cognitive ability in a DS model.

161 No effects of the early intervention on dietary behaviors, quality of life

162 e studies are warranted to determine whether early intervention or closer monitoring improves clinica

163 , low-birthweight infants were randomized to early (intervention) or delayed (usual policy) BCG.

164 d unresponsiveness at 4 weeks after stopping early intervention oral immunotherapy (4-SU), was assess

165 and health service provision to incentivise early intervention over provision of care only for advan

166 Building on long-term benefits of early intervention (Paper 2 of this Series) and increasi

167 icularly in infants, possibly as a result of early intervention policies.

168 elop complications, our results suggest that early intervention, preferably in a high-level intensive

169 m might offer a sought-after opportunity for early intervention, preservation of cognitive reserve, a

170 Early intervention prior to subepithelial fibrosis can l

171 potential novel HD therapeutic strategy for early intervention, prior to neuronal loss and clinical

172 mes, which may be partially reversed through early intervention programmes.

173 Early intervention programs for drug and alcohol misuse

174 These new findings suggest that early intervention programs should target children with

175 luded an autism clinic and 6 community-based early intervention programs that primarily serve low-inc

176 e individualized sessions by existing staff (early intervention programs) or research staff without f

177 form development of effective preventive and early intervention programs.

178 We used follow-up data from the Bucharest Early Intervention Project (BEIP), a randomised controll

179 8-y-old Romanian children from the Bucharest Early Intervention Project and the influence of attachme

180 We present results from the Bucharest Early Intervention Project examining whether randomized

181 The Bucharest Early Intervention Project is a randomized clinical tria

182 The Bucharest Early Intervention Project is a unique randomized contro

183 Children enrolled in the Bucharest Early Intervention Project underwent a T1-weighted MRI p

184 Data were drawn from the Bucharest Early Intervention Project, a cohort of children raised

185 ICIPANTS: Data were drawn from the Bucharest Early Intervention Project, a cohort of children raised

186 Follow-up analyses revealed that early intervention promoted more normative white matter

187 chosis cases, 16-35 years old, presenting to early intervention psychosis services in the East of Eng

188 chosis cases, 16-35 years old, presenting to early intervention psychosis services in the East of Eng

189 or urban settings since the introduction of early intervention psychosis services.

190 0 years old, exists in populations served by early intervention psychosis services.

191 ification of infants at risk and could guide early intervention regimens.

192 Hence, although early interventions remain critical, interventions to im

193 e the outcome variability that characterizes early intervention research at present, and provide for

194 reatment of inherited retinal diseases, with early intervention resulting in the best potential gain.

195 allograft dysfunction (IGD) might allow for early intervention(s) to preserve functional islet mass.

196 innate antiviral activity that vaccines and early interventions seek to exploit/enhance.

197 at high risk of developing psychosis to the early intervention service per practice site.

198 ants to receive social recovery therapy plus early intervention services (n=76) or early intervention

199 y plus early intervention services (n=76) or early intervention services alone (n=79); the intention-

200 therapy plus early intervention services or early intervention services alone.

201 h (95% CI 2.5-13.6; p=0.0050) compared with early intervention services alone.

202 We aimed to assess the efficacy of early intervention services augmented with social recove

203 Violent behavior at 6 or 12 months following early intervention services entry.

204 non-affective psychosis, had been clients of early intervention services for 12-30 months, and had pe

205 Provision of early intervention services has increased the rate of so

206 This study included 6 early intervention services in 5 geographical locations

207 intervention for people with psychosis using early intervention services in the UK.

208 rolled trial (SUPEREDEN3) at four specialist early intervention services in the UK.

209 EN (Evaluating the Development and Impact of Early Intervention Services in the West Midlands) Study

210 t meet existing eligibility requirements for early intervention services in their state.

211 ix), to receive social recovery therapy plus early intervention services or early intervention servic

212 Social recovery therapy plus early intervention services was associated with an incre

213 thesis was that social recovery therapy plus early intervention services would lead to improvements i

214 23 (26.7%) received first-time referrals for early intervention services, 16 (13.8%) received referra

215 is who received social recovery therapy plus early intervention services.

216 Studies of early intervention show mixed findings.

217 Early intervention significantly hastened return to phon

218 However, early intervention significantly reduces the incidence o

219 w is timely given the increasing interest in early intervention strategies and new opportunities to i

220 In summary, early intervention strategies can be based robustly just

221 Collectively, our findings argue for early intervention strategies designed to mitigate skin

222 These findings might help to guide early intervention strategies for at-risk youths.

223 These findings are important for designing early intervention strategies for secondary prevention o

224 ified serum biomarkers that allow testing of early intervention strategies in patients at the highest

225 oplastic progression may help in formulating early intervention strategies.

226 the utility of addressing these symptoms in early intervention strategies.

227 sis, expanding the repertoire of targets for early intervention strategies.

228 010 to 2012 including dissemination studies, early intervention studies and studies involving prescho

229 Dissemination studies and early intervention studies show mixed findings and furth

230 These data provide a framework for early intervention studies to facilitate safer applicati

231 omycin-injury IPF model, we demonstrate that early-intervention suicide-gene-mediated senescent cell

232 trate that, contrary to current thinking, an early intervention targeting NOD-like receptor family, p

233 This provides a rationale for early intervention, targeting the possible delay, reduct

234 absence--offers a promising opportunity for early intervention that could build on the apparent pres

235 lable evidence about cerebral palsy-specific early intervention that should follow early diagnosis to

236 These findings highlight the need for early interventions that can improve treatment outcomes

237 ntification may in turn facilitate access to early interventions that could prevent a life spent stru

238 Offering hope, early interventions that place institutionalised childre

239 se and whether they may contribute to design early interventions that prevent subsequent disease, inc

240 Army has developed Battlemind postdeployment early interventions that reduce risk for the disorder.

241 Therefore, these findings support early intervention therapy for individuals with T1D.

242 allocation of resources during the critical early intervention time-period.

243 These findings suggest that early intervention to change these modifiable risk facto

244 lity changes could afford an opportunity for early intervention to forestall tissue damage in newly f

245 al targets across multiple organ systems for early intervention to improve cardiometabolic health.

246 Early intervention to interrupt transmission may be most

247 hese known social risk factors and providing early intervention to negate long-term sequelae.

248 ce of prompt referral to diagnostic-specific early intervention to optimize infant motor and cognitiv

249 ized controlled trial tested the efficacy of early intervention to prevent adult psychopathology and

250 idual disease (MRD) following HCT may permit early intervention to prevent clinical relapse; however,

251 rapy, suggesting that careful monitoring and early intervention to prevent glaucoma is warranted with

252 s an integrated approach, which includes the early intervention to prevent or delay the disease progr

253 ctor for MCI and may provide a substrate for early intervention to prevent or delay the onset and pro

254 ecurrent pneumothorax who would benefit from early intervention to prevent recurrence.

255 ression in children could be used to promote early intervention to reduce the likelihood of developin

256 ents with cirrhosis should be prevention and early intervention to stabilise disease progression and

257 provided little support for the idea that an early intervention to support household income has a lar

258 ch will allow the implementation of the most early intervention to take place, before the irreversibl

259 on of these gene variations is important for early intervention to treat deadly diseases and provide

260 to support the use of routine screening and early interventions to prevent and treat suicidal ideati

261 e to aIMT and cIMT may help in the design of early interventions to prevent cardiovascular disease.

262 ased screening approaches that might lead to early interventions to prevent LOS in high risk infants.

263 th or without MCI is a promising approach in early interventions to prevent or slow progression to de

264 hout known CVD highlights an opportunity for early interventions to prevent progression of cardiovasc

265 Early interventions to prevent progression of kidney dis

266 o-backplate membranes as well as to identify early interventions to prevent progression of thin membr

267 aging, and they suggest the possibility that early interventions to promote certain health behaviors

268 est prevention of AD can be achieved through early interventions to protect the skin barrier.

269 involvement of fathers as well as mothers in early interventions to reduce the prevalence of adolesce

270 Early interventions to tackle parental mental disorders

271 This may have implications for early-intervention treatment, using protein rescue strat

272 ts enrolled in the Acute Catheterization and Early Intervention Triage Strategy (ACUITY) trial, 1772

273 monitoring and as quantitative endpoints in early intervention trials in children with CF.

274 In high-risk children, early intervention using different hydrolyzed formulas h

275 Early intervention was less than 20 hours after hospital

276 contrast, in the selective high-risk sample, early intervention was not associated with improved long

277 suitable for clinical trials testing whether early intervention will slow the development and/or prog

278 EGFR mutation could potentially benefit from early intervention with a combination of EGFR and Met in

279 ings support the rationale for investigating early intervention with a KMO inhibitor, with the aim of

280 er recovered, highlighting the importance of early intervention with A1PI treatment.

281 In patients with acute heart failure, early intervention with an intravenous vasodilator has b

282 of adequate treatment, timely diagnosis and early intervention with antifungal drugs are key factors

283 In mice with CIA, early intervention with APO866 inhibited synovial inflam

284 chronization Therapy (MADIT-CRT) showed that early intervention with cardiac-resynchronization therap

285 In addition, early intervention with cholinergic receptor muscarinic

286 We conclude that early intervention with CoQ in at-risk individuals may b

287 r dysfunction, and left bundle-branch block, early intervention with CRT-D was associated with a sign

288 Early intervention with disease-modifying anti-IBD drugs

289 Early intervention with GS-444217 significantly inhibite

290 Early intervention with intravitreal anti-VEGF medicatio

291 We studied the effect of an early intervention with mite-impermeable mattress covers

292 Early intervention with mite-impermeable mattress covers

293 s at risk for Parkinson's disease and permit early intervention with neuroprotective or disease-modif

294 disease who are most likely to benefit from early intervention with novel treatments.

295 An early intervention with PNS and/or pharmaceutical inhibi

296 ng of psychoeducation (i.e., recognition and early intervention with prodromal symptoms), communicati

297 In contrast, early intervention with selective high-risk samples may

298 Early intervention with severely antisocial children for

299 Early intervention with the combination of leucovorin an

300 antagonism is ineffective, and thus (3) that early intervention with TRP channel antagonists may atte