2,648 research outputs found

    Cardiovascular and cerebrovascular risk factors and events associated with second-generation antipsychotic compared to antidepressant use in a non-elderly adult sample: results from a claims-based inception cohort study

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    This is a study of the metabolic and distal cardiovascular/cerebrovascular outcomes associated with the use of second-generation antipsychotics (SGAs) compared to antidepressants (ADs) in adults aged 18-65 years, based on data from Thomson Reuters MarketScan (R) Research Databases 2006-2010, a commercial U.S. claims database. Interventions included clinicians\u27 choice treatment with SGAs (allowing any comedications) versus ADs (not allowing SGAs). The primary outcomes of interest were time to inpatient or outpatient claims for the following diagnoses within one year of SGA or AD discontinuation: hypertension, ischemic and hypertensive heart disease, cerebrovascular disease, diabetes mellitus, hyperlipidemia, and obesity. Secondary outcomes included the same diagnoses at last follow-up time point, i.e., not censoring observations at 365 days after SGA or AD discontinuation. Cox regression models, adjusted for age, gender, diagnosis of schizophrenia and mood disorders, and number of medical comorbidities, were run. Among 284,234 individuals, those within one year of exposure to SGAs versus ADs showed a higher risk of essential hypertension (adjusted hazard ratio, AHR=1.16, 95% CI: 1.12-1.21,

    A Zeeman Slower based on magnetic dipoles

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    A transverse Zeeman slower composed of an array of compact discrete neodymium magnets is considered. A simple and precise model of such a slower based on magnetic dipoles is developed. The theory of a general Zeeman slower is modified to include spatial nonuniformity of the slowing laser beam intensity due to its convergence and absorption by slowed atoms. The slower needs no high currents or water cooling and the spatial distribution of its magnetic field can be adjusted. In addition the slower provides a possibility to cool the slowed atoms transversally along the whole length of the slower. Such a slower would be ideal for transportable optical atomic clocks and their future applications in space physics.Comment: 17 pages, 9 figure

    Search for Λ + c → ϕ p π 0 and branching fraction measurement of Λ + c → K − π + p π 0

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    We have searched for the Cabibbo-suppressed decay Λ+c→ϕpπ0 in e+e− collisions using a data sample corresponding to an integrated luminosity of 915 fb−1. The data were collected by the Belle experiment at the KEKB e+e− asymmetric-energy collider running at or near the Υ(4S) and Υ(5S)resonances. No significant signal is observed, and we set an upper limit on the branching fraction of B(Λ+c→ϕpπ0)\u3c15.3×10−5 at 90% confidence level. The contribution of nonresonant Λ+c→K+K−pπ0 decays is found to be consistent with zero, and the corresponding upper limit on its branching fraction is set to be B(Λ+c→K+K−pπ0)NR\u3c6.3×10−5 at 90% confidence level. We also search for an intermediate hidden-strangeness pentaquark decay P+s→ϕp. We see no evidence for this intermediate decay and set an upper limit on the product branching fraction of B(Λ+c→P+sπ0)×B(P+s→ϕp)\u3c8.3×10−5 at 90% confidence level. Finally, we measure the branching fraction for the Cabibbo-favored decay Λ+c→K−π+pπ0; the result is B(Λ+c→K−π+pπ0)=(4.42±0.05(stat)±0.12(syst)±0.16(norm))%, which is the most precise measurement to date

    Towards many colors in FISH on 3D-preserved interphase nuclei

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    The article reviews the existing methods of multicolor FISH on nuclear targets, first of all, interphase chromosomes. FISH proper and image acquisition are considered as two related components of a single process. We discuss (1) M-FISH (combinatorial labeling + deconvolution + widefield microscopy); (2) multicolor labeling + SIM (structured illumination microscopy); (3) the standard approach to multicolor FISH + CLSM (confocal laser scanning microscopy; one fluorochrome - one color channel); (4) combinatorial labeling + CLSM; (5) non-combinatorial labeling + CLSM + linear unmixing. Two related issues, deconvolution of images acquired with CLSM and correction of data for chromatic Z-shift, are also discussed. All methods are illustrated with practical examples. Finally, several rules of thumb helping to choose an optimal labeling + microscopy combination for the planned experiment are suggested. Copyright (c) 2006 S. Karger AG, Basel

    Clinical response to long-term propranolol therapy in hyperthyroidism

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    Urethral metastasis from non-seminomatous germ cell tumor: a case report

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    <p>Abstract</p> <p>Introduction</p> <p>We present a case of nonseminomatous germ cell tumor of the testes with acute urinary retention secondary to urethral metastasis. This presentation, and similar cases of urethral metastasis from this tumor, have not been reported previously.</p> <p>Case presentation</p> <p>A 35-year-old Caucasian man presented to hospital with a history of acute urinary retention. On examination he was found to have right testicular enlargement with raised β-human chorionic gonadotrophin, serum α-fetoprotein and lactate dehydrogenase levels. He underwent radical left inguinal orchidectomy and histology confirmed a nonseminomatous germ cell tumor of the testes. Cystoscopy carried out due to urinary retention showed penile metastasis and the biopsy confirmed metastatic malignant undifferentiated teratoma. Staging computed tomography scan and magnetic resonance imaging of the pelvis showed pulmonary, pelvic nodal, ischial and penile metastasis. The diagnosis of the International Germ Cell Cancer Collaborative Group of poor prognosis metastatic nonseminomatous germ cell tumor was made, following which he received four cycles of bleomycin, etoposide and cisplatin chemotherapy with curative intent. He had a complete marker and an excellent radiological response. He is currently under follow up.</p> <p>Conclusion</p> <p>The unusual presentation of lymphovascular spread in this case of nonseminomatous germ cell tumor highlights the need to include routine pelvic imaging in the assessment and follow up of testicular cancer.</p

    The Color Dipole Picture of low-x DIS: Model-Independent and Model-Dependent Results

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    We present a detailed examination of the color-dipole picture (CDP) of low-xx deep inelastic scattering. We discriminate model-independent results, not depending on a specific parameterization of the dipole cross section, from model-dependent ones. The model-independent results include the ratio of the longitudinal to the transverse photoabsorption cross section at large Q2Q^2, or equivalently the ratio of the longitudinal to the unpolarized proton structure function, FL(x,Q2)=0.27F2(x,Q2)F_L (x,Q^2)=0.27 F_2 (x, Q^2), as well as the low-xx scaling behavior of the total photoabsorption cross section σγp(W2,Q2)=σγp(η(W2,Q2))\sigma_{\gamma^*p} (W^2, Q^2)=\sigma_{\gamma^*p} (\eta (W^2, Q^2)) as log(1/η(W2,Q2))\log (1 / \eta (W^2, Q^2)) for η(W2,Q2)<1\eta (W^2, Q^2) <1, and as 1/η(W2,Q2)1/\eta (W^2, Q^2) for η(W2,Q2)1\eta (W^2, Q^2) \gg 1. Here, η(W2,Q2)\eta (W^2, Q^2) denotes the low-xx scaling variable, η(W2,Q2)=(Q2+m02)/Λsat2(W2)\eta (W^2, Q^2)=(Q^2 + m^2_0) / \Lambda^2_{sat} (W^2) with Λsat2(W2)\Lambda^2_{sat} (W^2) being the saturation scale. The model-independent analysis also implies limW2,Q2fixedσγp(W2,Q2)/σγp(W2)1\lim\limits_{W^2\rightarrow\infty, Q^2 {\rm fixed}} \sigma_{\gamma^*p} (W^2, Q^2) / \sigma_{\gamma p} (W^2) \rightarrow 1 at any Q2Q^2 for asymptotically large energy, WW. Consistency with pQCD evolution determines the underlying gluon distribution and the numerical value of C2=0.29C_2 = 0.29 in the expression for the saturation scale, Λ2(W2)(W2)C2\Lambda^2 (W^2) \sim (W^2)^{C_2}. In the model-dependent analysis, by restricting the mass of the actively contributing qqˉq \bar q fluctuations by an energy-dependent upper bound, we extend the validity of the color-dipole picture to xQ2/W20.1x \cong Q^2 / W^2 \le 0.1. The theoretical results agree with the world data on DIS for 0.036GeV2Q2316GeV20.036 {\rm GeV}^2 \le Q^2 \le 316 {\rm GeV}^2.Comment: 77 pages, 30 figure
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