3,941 research outputs found
Time-dependent response of scoliotic curvature to orthotic intervention: when should a radiograph be obtained after putting on or taking off a spinal orthosis?
STUDY DESIGN:
A prospective study; 2-group design.
OBJECTIVE:
This study aims to assess the time response of scoliotic spines to orthotic intervention using clinical ultrasound.
SUMMARY OF BACKGROUND DATA:
Patients with moderate adolescent idiopathic scoliosis are generally advised orthotic treatment. However, the time to reach maximum correction after donning spinal orthosis or the time to return to pretreatment curvature after doffing spinal orthosis is not fully understood.
METHOD:
Subjects were divided into 2 groups, the don-orthosis group and the doff-orthosis group where the time reaching maximum correction and the time returning to pretreatment curvature were investigated accordingly. To avoid excessive radiation exposure via obtaining repeated radiographs, a validated method of estimating Cobb angle using radiation-free clinical ultrasound was applied at an interval of every 30 minutes up to 180 minutes. The spinal flexibility (estimated from supine radiographs) and body mass index were collected from the subjects for analyses.
RESULT:
Nine female patients with adolescent idiopathic scoliosis were recruited. There was no immediate change in the Cobb angles. A change of more than 5° could be observed in both groups only after 30 minutes and maximum change was found at/after 120 minutes. In the doff-orthosis group, the subject with the lowest body mass index took the longest time to increase more than 5° after doffing spinal orthosis. In the don-orthosis group, the subject with the highest body mass index took the longest time to achieve curve correction more than 5°.
CONCLUSION:
This investigation demonstrated that there is a time lag between application of spinal orthosis and its effect on scoliotic curvature. This is likely due to the low-stiff and viscoelastic properties of the spine. The clinical relevance of this study is that for patients with scoliosis undergoing orthotic treatment, radiograph should not be obtained within 2 hours of putting on or taking off spinal orthosis because it may not show the maximum effect.
LEVEL OF EVIDENCE: 4.postprin
Search for the Elusive Higgs Boson Using Jet Structure at LHC
We consider the production of a light non-standard model Higgs boson of order
100~\GEV with an associated boson at CERN Large Hadron Collider. We focus
on an interesting scenario that, the Higgs boson decays predominately into two
light scalars with mass of few GeV which sequently decay into four
gluons, i.e. . Since is much lighter than the Higgs
boson, it will be highly boosted and its decay products, the two gluons, will
move close to each other, resulting in a single jet for decay in the
detector. By using electromagnetic calorimeter-based and jet substructure
analyses, we show in two cases of different masses that it is quite
promising to extract the signal of Higgs boson out of large QCD background.Comment: 20 pages, 7 figure
Neuroprotective effects of minocycline on double-stranded RNA-induced neurotoxicity in cultured cortical neurons
1. Minocycline, memantine,and glycoconjugate were assessed for their ability to protect cultured primary cortical neurons against double-stranded RNA-induced neurotoxicity. 2. Minocycline but not memantine or glycoconjugate protected cultured cells and warrants further investigation.published_or_final_versio
Isotopic dependence of predissociation linewidths in the Schumann-Runge bands of oxygen
It is demonstrated that, according to semi-classical theory, the isotopic dependence of the predissociation linewidths in the Schumann-Runge bands of oxygen cannot be removed by simple scaling of the reduced mass. This is in contrast to the isotopic dependence of the predissociated vibrational energy levels. ©1995 American Institute of Physics.published_or_final_versio
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SARS CoV subunit vaccine: Antibodymediated neutralisation and enhancement
1. A SARS vaccine was produced based on recombinant native full-length Spike-protein trimers (triSpike) and efficient establishment of a vaccination procedure in rodents. 2. Antibody-mediated enhancement of SARS-CoV infection with anti-SARS-CoV Spike immune-serum was observed in vitro. 3. Antibody-mediated infection of SARS-CoV triggers entry into human haematopoietic cells via an FcγR-dependent and ACE2-, pH-, cysteine-protease-independent pathways. 4. The antibody-mediated enhancement phenomenon is not a mandatory component of the humoral immune response elicited by SARS vaccines, as pure neutralising antibody only could be obtained. 5. Occurrence of immune-mediated enhancement of SARS-CoV infection raises safety concerns regarding the use of SARS-CoV vaccine in humans and enables new ways to investigate SARS pathogenesis (tropism and immune response deregulation)
Antibody-dependent infection of human macrophages by severe acute respiratory syndrome coronavirus
Public health risks associated to infection by human coronaviruses remain considerable and vaccination is a key option for preventing the resurgence of severe acute respiratory syndrome coronavirus (SARS-CoV). We have previously reported that antibodies elicited by a SARS-CoV vaccine candidate based on recombinant, full-length SARS-CoV Spike-protein trimers, trigger infection of immune cell lines. These observations prompted us to investigate the molecular mechanisms and responses to antibody-mediated infection in human macrophages.published_or_final_versio
Antibody-dependent enhancement of SARS coronavirus infection and its role in the pathogenesis of SARS
1. Anti-SARS-CoV spike antibodies promote infection of primary human immune cells by SARS-CoV. 2. The antibody-dependent enhancement (ADE) infection pathway grants SARS-CoV an opportunity to infect primary human macrophages, but it does not sustain productive viral replication in the infected cells. 3. ADE of SARS-CoV infection does not alter pro-inflammatory gene expression profile of primary human macrophages. 4. Infectivity of SARS-CoV does not rely solely on the potency of target cells to bind — via Fcγ receptor II (CD32) — infectious immune complexes, but depends on the properties of the intracellular domain of the FcγRII. 5. Occurrence of ADE of SARS-CoV infection into human primary macrophages, without alteration to their pro-inflammatory properties, advocates cautious development of SARS-CoV vaccine in humans, and provides new ways of investigation to understand the pathogenesis of SARS.published_or_final_versio
Higgs Mass from D-Terms: a Litmus Test
We explore supersymmetric theories in which the Higgs mass is boosted by the
non-decoupling D-terms of an extended gauge symmetry, defined here to
be a general linear combination of hypercharge, baryon number, and lepton
number. Crucially, the gauge coupling, , is bounded from below to
accommodate the Higgs mass, while the quarks and leptons are required by gauge
invariance to carry non-zero charge under . This induces an irreducible
rate, BR, for relevant to
existing and future resonance searches, and gives rise to higher dimension
operators that are stringently constrained by precision electroweak
measurements. Combined, these bounds define a maximally allowed region in the
space of observables, (BR, ), outside of which is excluded by
naturalness and experimental limits. If natural supersymmetry utilizes
non-decoupling D-terms, then the associated boson can only be observed
within this window, providing a model independent `litmus test' for this broad
class of scenarios at the LHC. Comparing limits, we find that current LHC
results only exclude regions in parameter space which were already disfavored
by precision electroweak data.Comment: 7 pages, 9 figure
Integrated human papillomavirus analysis as an adjunct for triage of atypical cervical cytology
published_or_final_versio
Higgs boson enhancement effects on squark-pair production at the LHC
We study the Higgs boson effects on third-generation squark-pair production
in proton-proton collision at the CERN Large Hadron Collider (LHC), including
\Stop \Stop^*, \Stop\Sbot^*, and \Sbot \Sbot^*. We found that substantial
enhancement can be obtained through s-channel exchanges of Higgs bosons at
large , at which the enhancement mainly comes from , , and initial states. We compute the complete set of electroweak
(EW) contributions to all production channels. This completes previous
computations in the literature. We found that the EW contributions can be
significant and can reach up to 25% in more general scenarios and at the
resonance of the heavy Higgs boson. The size of Higgs enhancement is comparable
or even higher than the PDF uncertainties and so must be included in any
reliable analysis. A full analytical computation of all the EW contributions is
presented.Comment: 23 pages, 7 figures, 1 tabl
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