309 research outputs found

    Economic policy during the long 19th century

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    This chapter provides an overview of the political decision-making process and the modernisation of the state apparatus during the 19th century. It discusses the legal capacity of the states which acted either as a constraint on policymakers or enabled them to pursue and enforce a certain set of economic decisions. At the beginning of the 19th century, the region was divided up among the Austrian Empire, the Ottoman Empire, and the Russian Empire. The late 19th century and the remaining time up to the war saw a rise in protectionism, a growing share of state ownership in infrastructure, and a growing government share in gross domestic product (GDP). In Russia, where serfs belonged either to the state or to private persons and accounted for more than half the population at the beginning of the 19th century, the emancipation of state serfs started in the 1840s, and that of serfs in the private sector followed in 1861

    Reliable Sequential Activation of Neural Assemblies by Single Pyramidal Cells in a Three-Layered Cortex

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    Recent studies reveal the occasional impact of single neurons on surround firing statistics and even simple behaviors. Exploiting the advantages of a simple cortex, we examined the influence of single pyramidal neurons on surrounding cortical circuits. Brief activation of single neurons triggered reliable sequences of firing in tens of other excitatory and inhibitory cortical neurons, reflecting cascading activity through local networks, as indicated by delayed yet precisely timed polysynaptic subthreshold potentials. The evoked patterns were specific to the pyramidal cell of origin, extended over hundreds of micrometers from their source, and unfolded over up to 200 ms. Simultaneous activation of pyramidal cell pairs indicated balanced control of population activity, preventing paroxysmal amplification. Single cortical pyramidal neurons can thus trigger reliable postsynaptic activity that can propagate in a reliable fashion through cortex, generating rapidly evolving and non-random firing sequences reminiscent of those observed in mammalian hippocampus during "replay" and in avian song circuits

    Reconstruction of human thorax from CT images

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    3D printing, as a rapid prototyping method is become more common nowadays world widely, including medicine too. The purpose of this article is to reveal the potential of using 3D printing in medicine, especially with a specific example of making a human thorax model from the very beginning of imaging diagnose to the physical model. There will be shown in details how the model of bones, lungs and heart had been created. The circumstances of the 3D printing will be discussed too

    Egyedi kĂ©zrögzĂ­tƑ fejlesztĂ©se Ă©s gyĂĄrtĂĄsa 3D nyomtatĂĄssal

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    Az additív gyártástechnológiák napjainkban egyre több területen jelennek meg, melyek közül az egyik legfontosabb az egészségügy. Segítségével egyedi tervezésƱ, személyre szabott kezelést nyújthatunk a betegeknek, ami a modern orvostudomány egyik alapja. A napjainkban alkalmazott törésrögzítés több szempontból is elavult, de a rendszer mérete, valamint az eljárás alacsony ára miatt nehezen fejleszthetƑ. A hagyományos módszer sokszor kényelmetlen, nehézkes és kellemetlen. Ezt a törésrögzítési folyamatot egyedivé és könnyebbé teszi az additív gyártástechnológia és az eredményeképpen elkészült gyógyászati segédeszköz. A kutatás célja egy olyan eljárás kidolgozása, amely a mai egészségügyi rendszerben alkalmazott törésrögzítésre alternatívát nyújt. A hagyományos és a mƱanyag gipszkötés is számos hátránnyal rendelkezik, melyek az egyedi tervezésƱ és gyártású rögzítƑvel kiküszöbölhetƑvé válhatnak. A cél egy olyan eljárás és a folyamat során létrehozott termék bemutatása, amely a beteg státuszának felvételétƑl a kész ortézis kézhezvételéig tart. A rögzítƑ elkészítésének fƑbb folyamatpontjai: a beteg státuszának felvétele, kéz digitális letapogatása, 3D-s modell elkészítése, optimalizálása, a rögzítƑ nyomtatása, utómunkálatok elvégzése, tesztelése, majd végül a beteg tájékoztatása a használattal kapcsolatban

    Serum sclerostin levels in renal cell carcinoma patients with bone metastases

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    Sclerostin has been proposed as a potent inhibitor of bone formation. Sclerostin antibodies are under clinical development to treat osteoporosis and metastatic bone disease. Serum sclerostin level is elevated in multiple myeloma, an osteolytic malignancy, where it might serve as predictive marker for the use of sclerostin-directed antibodies. As renal cell carcinoma (RCC) patients often present with osteolytic metastases, we aimed to investigate serum sclerostin levels in RCC patients. Our study included 53 RCC patients (19 with bone metastases, 25 with visceral metastases and 9 with localized disease) and 53 age- and gender-matched non-osteoporotic controls. Frozen serum samples were subjected to sclerostin quantitative sandwich ELISA. The mean serum sclerostin levels of RCC patients and controls were 45.8 pmol/l and 45.1 pmol/l, respectively (p = 0.86). Analysis of variance showed no difference between the subgroups of RCC patients with regard to visceral or bone metastases or localized disease (p = 0.22). There was no significant association between eGFR (estimated glomerular filtration rate) and serum sclerostin levels in RCC patients (r = 0.05; p = 0.74) and controls (r = 0.06; p = 0.68). Our results indicate that serum sclerostin levels appear not to be a valuable biomarker to assess the occurrence of bone metastases in RCC patients

    Denosumab compared with risedronate in postmenopausal women suboptimally adherent to alendronate therapy: Efficacy and safety results from a randomized open-label study

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    Denosumab has been shown to reduce new vertebral, nonvertebral, and hip fractures in postmenopausal women with osteoporosis. In subjects who were treatment-naive or previously treated with alendronate, denosumab was associated with greater gains in bone mineral density (BMD) and decreases in bone turnover markers when compared with alendronate-treated subjects. This trial was designed to compare the efficacy and safety of denosumab with risedronate over 12 months in postmenopausal women who transitioned from daily or weekly alendronate treatment and were considered to be suboptimally adherent to therapy. In this randomized, open-label study, postmenopausal women aged ≄55 years received denosumab 60 mg subcutaneously every 6 months or risedronate 150 mg orally every month for 12 months. Endpoints included percentage change from baseline in total hip BMD (primary endpoint), femoral neck, and lumbar spine BMD at month 12, and percentage change from baseline in sCTX-1 at months 1 and 6. Safety was also assessed. A total of 870 subjects were randomized (435, risedronate; 435, denosumab) who had a mean (SD) age of 67.7 (6.9) years, mean (SD) BMD T-scores of -1.6 (0.9), -1.9 (0.7), and -2.2 (1.2) at the total hip, femoral neck, and lumbar spine, respectively, and median sCTX-1 of 0.3 ng/mL at baseline. At month 12, denosumab significantly increased BMD compared with risedronate at the total hip (2.0% vs 0.5%), femoral neck (1.4% vs 0%), and lumbar spine (3.4% vs 1.1%; p<0.0001 at all sites). Denosumab significantly decreased sCTX-1 compared with risedronate at month 1 (median change from baseline of -78% vs -17%; p<0.0001) and month 6 (-61% vs -23%; p<0.0001). Overall and serious adverse events were similar between groups. In postmenopausal women who were suboptimally adherent to alendronate therapy, transitioning to denosumab was well tolerated and more effective than risedronate in increasing BMD and reducing bone turnover

    Rechargeable Batteries of the Future—The State of the Art from a BATTERY 2030+ Perspective

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    The development of new batteries has historically been achieved through discovery and development cycles based on the intuition of the researcher, followed by experimental trial and error—often helped along by serendipitous breakthroughs. Meanwhile, it is evident that new strategies are needed to master the ever-growing complexity in the development of battery systems, and to fast-track the transfer of findings from the laboratory into commercially viable products. This review gives an overview over the future needs and the current state-of-the art of five research pillars of the European Large-Scale Research Initiative BATTERY 2030+, namely 1) Battery Interface Genome in combination with a Materials Acceleration Platform (BIG-MAP), progress toward the development of 2) self-healing battery materials, and methods for operando, 3) sensing to monitor battery health. These subjects are complemented by an overview over current and up-coming strategies to optimize 4) manufacturability of batteries and efforts toward development of a circular battery economy through implementation of 5) recyclability aspects in the design of the battery

    Relationship between bone turnover and left ventricular function in primary hyperparathyroidism: The EPATH trial

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    Observational studies suggested a link between bone disease and left ventricular (LV) dysfunction that may be pronounced in hyperparathyroid conditions. We therefore aimed to test the hypothesis that circulating markers of bone turnover correlate with LV function in a cohort of patients with primary hyperparathyroidism (pHPT). Cross-sectional data of 155 subjects with pHPT were analyzed who participated in the \uaaEplerenone in Primary Hyperparathyroidism \uba (EPATH) Trial. Multivariate linear regression analyses with LV ejection fraction (LVEF, systolic function) or peak early transmitral filling velocity (e', diastolic function) as dependent variables and N-terminal propeptide of procollagen type 1 (P1NP), osteocalcin (OC), bone-specific alkaline phosphatase (BALP), or beta-crosslaps (CTX) as the respective independent variable were performed. Analyses were additionally adjusted for plasma parathyroid hormone, plasma calcium, age, sex, HbA1c, body mass index, mean 24-hours systolic blood pressure, smoking status, estimated glomerular filtration rate, antihypertensive treatment, osteoporosis treatment, 25-hydroxy vitamin D and N-terminal probrain B-type natriuretic peptide. Independent relationships were observed between P1NP and LVEF (adjusted \u3b2-coefficient = 0.201, P = 0.035) and e' (\u3b2 = 0.188, P = 0.042), respectively. OC (\u3b2 = 0.192, P = 0.039) and BALP (\u3b2 = 0.198, P = 0.030) were each independently related with e'. CTX showed no correlations with LVEF or e'. In conclusion, high bone formation markers were independently and paradoxically related with better LV diastolic and, partly, better systolic function, in the setting of pHPT. Potentially cardio-protective properties of stimulated bone formation in the context of hyperparathyroidism should be explored in future studies
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