145 research outputs found
Search for a 33.9 MeV/c^2 Neutral Particle in Pion Decay
The E815 (NuTeV) neutrino experiment has performed a search for a 33.9
MeV/c^2 weakly-interacting neutral particle produced in pion decay. Such a
particle may be responsible for an anomaly in the timing distribution of
neutrino interactions in the KARMEN experiment. E815 has searched for this
particle's decays in an instrumented decay region; no evidence for this
particle was found. The search is sensitive to pion branching ratios as low as
10^-13.Comment: 4 pages; 5 figure
A scheme with two large extra dimensions confronted with neutrino physics
We investigate a particle physics model in a six-dimensional spacetime, where
two extra dimensions form a torus. Particles with Standard Model charges are
confined by interactions with a scalar field to four four-dimensional branes,
two vortices accommodating ordinary type fermions and two antivortices
accommodating mirror fermions. We investigate the phenomenological implications
of this multibrane structure by confronting the model with neutrino physics
data.Comment: LATEX, 24 pages, 9 figures, minor changes in the tex
Constraints on a Massive Dirac Neutrino Model
We examine constraints on a simple neutrino model in which there are three
massless and three massive Dirac neutrinos and in which the left handed
neutrinos are linear combinations of doublet and singlet neutrinos. We examine
constraints from direct decays into heavy neutrinos, indirect effects on
electroweak parameters, and flavor changing processes. We combine these
constraints to examine the allowed mass range for the heavy neutrinos of each
of the three generations.Comment: latex, 29 pages, 7 figures (not included), MIT-CTP-221
Clinically Feasible Microstructural MRI to Quantify Cervical Spinal Cord Tissue Injury Using DTI, MT, and T2*-Weighted Imaging:Assessment of Normative Data and Reliability
Forty healthy subjects underwent T2WI, DTI, magnetization transfer, and T2*WI at 3T in BACKGROUND AND PURPOSE: DTI, magnetization transfer, T2*-weighted imaging, and cross-sectional area can quantify aspects of spinal cord microstructure. However, clinical adoption remains elusive due to complex acquisitions, cumbersome analysis, limited reliability, and wide ranges of normal values. We propose a simple multiparametric protocol with automated analysis and report normative data, analysis of confounding variables, and reliability. MATERIALS AND METHODS: Forty healthy subjects underwent T2WI, DTI, magnetization transfer, and T2*WI at 3T in RESULTS: T2*WI WM/GM showed lower intersubject coefficient of variation (3.5%) compared with magnetization transfer ratio (5.8%), fractional anisotropy (6.0%), and cross-sectional area (12.2%). Linear correction of cross-sectional area with cervical cord length, fractional anisotropy with age, and magnetization transfer ratio with age and height led to decreased coefficients of variation (4.8%, 5.4%, and 10.2%, respectively). Acceptable reliability was achieved for all metrics/levels (test-retest coefficient of variation <5%), with T2*WI WM/GM comparing favorably with fractional anisotropy and magnetization transfer ratio. DTI with and without cardiac triggering showed no significant differences for fractional anisotropy and test-retest coefficient of variation. CONCLUSIONS: Reliable multiparametric assessment of spinal cord microstructure is possible by using clinically suitable methods. These results establish normalization procedures and pave the way for clinical studies, with the potential for improving diagnostics, objectively monitoring disease progression, and predicting outcomes in spinal pathologies
Spinal cord grey matter segmentation challenge
An important image processing step in spinal cord magnetic resonance imaging is the ability to reliably and accurately segment grey and white matter for tissue specific analysis. There are several semi- or fully-automated segmentation methods for cervical cord cross-sectional area measurement with an excellent performance close or equal to the manual segmentation. However, grey matter segmentation is still challenging due to small cross-sectional size and shape, and active research is being conducted by several groups around the world in this field. Therefore a grey matter spinal cord segmentation challenge was organised to test different capabilities of various methods using the same multi-centre and multi-vendor dataset acquired with distinct 3D gradient-echo sequences. This challenge aimed to characterize the state-of-the-art in the field as well as identifying new opportunities for future improvements. Six different spinal cord grey matter segmentation methods developed independently by various research groups across the world and their performance were compared to manual segmentation outcomes, the present gold-standard. All algorithms provided good overall results for detecting the grey matter butterfly, albeit with variable performance in certain quality-of-segmentation metrics. The data have been made publicly available and the challenge web site remains open to new submissions. No modifications were introduced to any of the presented methods as a result of this challenge for the purposes of this publication
Primordial Nucleosynthesis with a Decaying Tau Neutrino
A comprehensive study of the effect of an unstable tau neutrino on primordial
nucleosynthesis is presented. The standard code for nucleosynthesis is modified
to allow for a massive decaying tau neutrino whose daughter products include
neutrinos, photons, pairs, and/or noninteracting (sterile) daughter
products. Tau-neutrino decays influence primordial nucleosynthesis in three
distinct ways: (i) the energy density of the decaying tau neutrino and its
daughter products affect the expansion rate tending to increase He, D, and
He production; (ii) electromagnetic (EM) decay products heat the EM plasma
and dilute the baryon-to-photon ratio tending to decrease He production and
increase D and He production; and (iii) electron neutrinos and
antineutrinos produced by tau-neutrino decays increase the weak rates that
govern the neutron-to-proton ratio, leading to decreased He production for
short lifetimes (\la 30\sec) and masses less than about 10\MeV and
increased He production for long lifetimes or large masses. The precise
effect of a decaying tau neutrino on the yields of primordial nucleosynthesis
and the mass-lifetime limits that follow depend crucially upon decay mode. We
identify four generic decay modes that serve to bracket the wider range of
possibilities:Comment: 27 pages, Latex, 12 Figures avaiable on request, FNAL--Pub--93/236-
Open-access quantitative MRI data of the spinal cord and reproducibility across participants, sites and manufacturers
In a companion paper by Cohen-Adad et al. we introduce the spine generic quantitative MRI protocol that provides valuable metrics for assessing spinal cord macrostructural and microstructural integrity. This protocol was used to acquire a single subject dataset across 19 centers and a multi-subject dataset across 42 centers (for a total of 260 participants), spanning the three main MRI manufacturers: GE, Philips and Siemens. Both datasets are publicly available via git-annex. Data were analysed using the Spinal Cord Toolbox to produce normative values as well as inter/intra-site and inter/intra-manufacturer statistics. Reproducibility for the spine generic protocol was high across sites and manufacturers, with an average inter-site coefficient of variation of less than 5% for all the metrics. Full documentation and results can be found at https://spine-generic.rtfd.io/. The datasets and analysis pipeline will help pave the way towards accessible and reproducible quantitative MRI in the spinal cord
Generic acquisition protocol for quantitative MRI of the spinal cord
Quantitative spinal cord (SC) magnetic resonance imaging (MRI) presents many challenges, including a lack of standardized imaging protocols. Here we present a prospectively harmonized quantitative MRI protocol, which we refer to as the spine generic protocol, for users of 3T MRI systems from the three main manufacturers: GE, Philips and Siemens. The protocol provides guidance for assessing SC macrostructural and microstructural integrity: T1-weighted and T2-weighted imaging for SC cross-sectional area computation, multi-echo gradient echo for gray matter cross-sectional area, and magnetization transfer and diffusion weighted imaging for assessing white matter microstructure. In a companion paper from the same authors, the spine generic protocol was used to acquire data across 42 centers in 260 healthy subjects. The key details of the spine generic protocol are also available in an open-access document that can be found at https://github.com/spine-generic/protocols. The protocol will serve as a starting point for researchers and clinicians implementing new SC imaging initiatives so that, in the future, inclusion of the SC in neuroimaging protocols will be more common. The protocol could be implemented by any trained MR technician or by a researcher/clinician familiar with MRI acquisition
Author Correction: Open-access quantitative MRI data of the spinal cord and reproducibility across participants, sites and manufacturers
- …