Neutrino energy reconstruction from one muon and one proton events

We propose a new method of selection of high purity charge current quasielastic neutrino events with a good reconstruction of interacting neutrino energy. Performance of the method was verified with several tests using GENIE, NEUT and NuWro Monte Carlo events generators with carbon and argon targets. The method can be useful in neutrino oscillation studies with a few GeV energy beams.Comment: 8 pages, 5 figure

Matrix exponential via Clifford algebras

We use isomorphism $\varphi$ between matrix algebras and simple orthogonal Clifford algebras \cl(Q) to compute matrix exponential ${e}^{A}$ of a real, complex, and quaternionic matrix A. The isomorphic image $p=\varphi(A)$ in \cl(Q), where the quadratic form $Q$ has a suitable signature $(p,q),$ is exponentiated modulo a minimal polynomial of $p$ using Clifford exponential. Elements of \cl(Q) are treated as symbolic multivariate polynomials in Grassmann monomials. Computations in \cl(Q) are performed with a Maple package `CLIFFORD'. Three examples of matrix exponentiation are given

Kappa-contraction from SUq(2)SU_q(2) to Eκ(2)E_{\kappa}(2)

We present contraction prescription of the quantum groups: from $SU_q(2)$ to $E_{\kappa}(2)$. Our strategy is different then one chosen in ref. [P. Zaugg, J. Phys. A {\bf 28} (1995) 2589]. We provide explicite prescription for contraction of $a, b, c$ and $d$ generators of $SL_q(2)$ and arrive at $^*$ Hopf algebra $E_{\kappa}(2)$.Comment: 3 pages, plain TEX, harvmac, to be published in the Proceedings of the 4-th Colloqium Quantum Groups and Integrable Systems, Prague, June 1995, Czech. J. Phys. {\bf 46} 265 (1996

Spectral functions for medium-sized nuclei

The spectral functions for calcium and argon are constructed. It is verified that their predictions for the quasielastic electron-nucleus cross sections in the energy range ~1 GeV agree with the data. The argon spectral function is then used to obtain the quasielastic neutrino-nucleus cross section.Comment: 3 pages, 3 figures, presented at 5th International Workshop on Neutrino-Nucleus Interactions in the Few-GeV Region (NuInt07), Fermilab, USA, 30.05-3.06.200

Factors influencing transfusion-associated HLA sensitization in patients bridged to heart transplantation using ventricular assist device.

BackgroundBridging heart failure patients with mechanical ventricular assist devices (VAD) enables access to transplantation. However, VAD is associated with increased risk for anti-HLA antibodies associated with rejection of subsequent allografts. Factors determining alloantibody formation in these patients remain undefined.MethodsWe performed a single-center retrospective cohort study of 164 patients undergoing heart transplantation from 2014 to 2017. Medical records including use of VAD, transfused blood products, anti-HLA antibody testing, crossmatch, and time to transplant were evaluated.ResultsPatients received an average of 13.8 red blood cell and 1.9 single-donor platelet units associated with VAD. There was a 28.7% increase in the incidence of anti-HLA antibodies after VAD. Development of anti-HLA antibodies did not correlate with volume or type of blood products, but with pre-VAD HLA sensitization status; relative risk of new alloantibodies in patients with pre-VAD antibodies was 3.5-fold higher than those without prior antibodies (P = .008). Development of new anti-HLA antibodies was associated with an increased time to transplant (169 vs 330 days, P = .013).ConclusionsOur findings indicate that the presence of anti-HLA antibodies pre-VAD was the most significant risk factor for developing additional antibodies post-VAD, suggesting that a subset of patients may be predisposed to alloantibody formation

C5AC_5^A axial form factor from bubble chamber experiments

A careful reanalysis of both Argonne National Laboratory and Brookhaven National Laboratory data for weak single pion production is done. We consider deuteron nuclear effects and normalization (flux) uncertainties in both experiments. We demonstrate that these two sets of data are in good agreement. For the dipole parametrization of $C_5^A(Q^2)$, we obtain $C_5^A(0)=1.19\pm 0.08$, $M_A=0.94\pm 0.03$ GeV. As an application we present the discussion of the uncertainty of the neutral current 1$\pi^0$ production cross section, important for the T2K neutrino oscillation experiment.Comment: 16 pages, 8 figures, 2 table

The analysis of renal artery cross-section area and kidney volume in computed tomography angiography

Background: The purpose of this study was to assess the relationship between renal artery cross-section area and kidney volume with consideration of anatomical variants of renal arteries, sexual dimorphism and lateralisation. Materials and methods: Two hundred and two patients, 104 women and 98 men, aged 57.3 ± 16 years were examined using computed tomography angiography (CTA) of abdominal aorta for various reasons. The cross-section areas of renal arteries were measured automatically with a vessel tracking programme and summed up on each side in case of the presence of additional renal arteries. The kidneys were measured manually. Results: Additional renal arteries (ARA) were found in 68 (33.7%) patients. Fifty-three (77.9%) of them had one, 11 (16.2%) two and 4 (5.9%) three ARAs. Bilateral ARAs occurred in 10 cases (14.7% patients with ARA). Proximal branching of renal artery occurred in 36 (8.4%) renal arteries. The cross-section area of the largest renal artery depended on the number of ipsilateral renal arteries. Mean cross-section area of the main left renal artery was larger than on the right side (28.52 mm2 vs. 25.36 mm2, p < 0.01) in the whole analysed group. Strong sexual dimorphism in renal artery cross-section area was observed (p < 0.01) in favour of men (31.3 mm2 in men and 22.9 mm2 in women). Mean total renal artery cross-section area has positively correlated with kidney volume (p < 10–13) in both sexes with Pearson correlation value of 0.5. Conclusions: The cross-section area of renal arteries correlated positively with kidney volume in both sexes. Presence of ARAs does not influence the sum of cross-section areas of renal arteries. In case of a difference between left and right renal artery cross-section area with symmetrical kidneys, it is necessary to look for ARA