818 research outputs found
Study of the feasibility and diagnostic accuracy of Proteomics and Next Generation Sequencing (NGS) for the investigation of neurosurgical cerebrospinal fluid infections.
Measurement of the Branching Fraction of the Decay in Fully Reconstructed Events at Belle
We present an analysis of the exclusive
decay, where represents an
electron or a muon, with the assumption of charge-conjugation symmetry and
lepton universality. The analysis uses the full data sample
collected by the Belle detector, corresponding to 711 fb of integrated
luminosity. We select the events by fully reconstructing one meson in
hadronic decay modes, subsequently determining the properties of the other
meson. We extract the signal yields using a binned maximum-likelihood fit to
the missing-mass squared distribution in bins of the invariant mass of the two
pions or the momentum transfer squared. We measure a total branching fraction
of , where the
uncertainties are statistical and systematic, respectively. This result is the
first reported measurement of this decay.Comment: 23 pages, 19 figure
Evidence for a vector charmonium-like state in
We report the measurement of via
initial-state radiation using a data sample of an integrated luminosity of
921.9 fb collected with the Belle detector at the and
nearby. We find evidence for an enhancement with a 3.4 significance in
the invariant mass of The measured mass and width
are
and ,
respectively. The mass, width, and quantum numbers of this enhancement are
consistent with the charmonium-like state at 4626 MeV/ recently reported
by Belle in The product of the cross section and the branching fraction of
is measured from
threshold to 5.6 GeV.Comment: 9 pages, 4 figure
Screening for cerebrovascular disorder on the basis of family history in asymptomatic children
Background: Cerebrovascular disorders represent a group of uncommon, heterogeneous, and complex conditions in children. We reviewed the screening practice for the detection of cerebrovascular disorder in asymptomatic children referred to our neurovascular service on the basis of a positive family history and parental and/or treating physician concern.Methods: Retrospective case-note review of referrals to our neurovascular service (July 2008-April 2018). Patients were included if the referral was made for screening, on the basis of a positive family history of cerebrovascular disorder. Symptomatic children, those with previous cranial imaging, or children under the care of a clinical geneticist (i.e. due to the child or their relative having HHT or mutations in KRIT1) were not eligible for inclusion.Results: Forty-one children were reviewed, 22 males (Median age 10.7 years, range 0.6-15.6 years). This represented 22% of the total number of referrals over a 10-year period. Twenty-nine children had an MRI/MRA brain. Twenty-eight children were referred due to a family history of intracranial aneurysm and/or subarachnoid haemorrhage, but only two had two first-degree relatives affected. Ten children were referred due to a family history of arteriovenous malformation. Three children were referred due to a family history of stroke. No cerebrovascular disease was detected during the study period (n = 29).Conclusions: Parental and/or physician concern generated a substantial number of referrals but no pathology was detected after screening. Whilst general screening guidance exists for the detection of intracranial aneurysms, consensus guidelines for the screening of children with a positive family history do not, but are required both to guide clinical practice and to assuage parental and/or physician concerns
Measurement of the branching fraction and time-dependent CP asymmetry for B⁰ → J/ψπ⁰ decays
We measure the branching fraction and time-dependent CP-violating asymmetry for B0→J/ψπ0 decays using a data sample of 711 fb−1 collected on the Υ(4S) resonance by the Belle experiment running at the KEKB e+e− collider. The branching fraction is measured to be B(B0→J/ψπ0)=[1.62±0.11(stat)±0.06(syst)]×10−5, which is the most precise measurement to date. The measured CP asymmetry parameters are S=−0.59±0.19(stat)±0.03(syst) and A=−0.15±0.14(stat)
+0.04
−0.03(syst). The mixing-induced CP asymmetry (S) differs from the case of no CP violation by 3.0 standard deviations, and the direct CP asymmetry (A) is consistent with zero
Measurement of B(B →dX) with B semileptonic tagging
We report the first direct measurement of the inclusive branching fraction B(B →DX) via B tagging in ee→Υ(5S) events. Tagging is accomplished through a partial reconstruction of semileptonic decays B→DXℓν, where X denotes unreconstructed additional hadrons or photons and ℓ is an electron or muon. With 121.4 fb of data collected at the Υ(5S) resonance by the Belle detector at the KEKB asymmetric-energy ee collider, we obtain B(B →DX)=(60.2±5.8±2.3)%, where the first uncertainty is statistical and the second is systematic
Observation of ee -> πππχ(1) and search for ee -> ϕχ(1) at = 10.9611.05 GeV
We report searches for the processes ee → πππχ and ee → ϕχ (J=1, 2) based on data samples collected by the Belle experiment at the KEKB collider. We report the first observation of the process ee → ππ and first evidence for ee → ωχbJ in the vicinity of the Υ(11020) resonance, with center-of-mass energies from 10.96 to 11.05 GeV. The significances for ππ and ωχbJ are greater than 5.3σ and 4.0σ, respectively. We also investigate the energy dependence of the ee →ππχbJ cross section, but we cannot determine whether the contributions are from the Υ(10860) and Υ(11020) resonances or nonresonant continuum processes. The signals for ee → ϕ are not significant, and the upper limits of the Born cross sections at the 90% confidence level are 0.7 and 1.0 pb for ee$^{-} → ϕχb1 and ϕχb2, respectively, for center-of-mass energies from 10.96 to 11.05 GeV
Measurement of the branching fraction of at Belle
Based on a data sample of 983 fb collected with the Belle detector at
the KEKB asymmetric-energy collider, we present the study of the
heavy-flavor-conserving decay with
reconstructed via its decay mode. The
branching fraction ratio is measured
to be . Combing with the world average value of
, the branching fraction
is deduced to be . Here, the uncertainties above are statistical,
systematic, and from , respectively.Comment: 5 pages, 4 figure
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