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2008: The lisp API, Autodesk Exchange, and Exchange APIs (C++ and Visual LISP) are removed, and the.NET API is deprecated. The Visual Studio Add-in and Visual LISP is deprecated in favour of the.NET API. As Autodesk Exchange 2007 (C++, Visual LISP and Visual Studio Add-in) is discontinued, the C++ and Visual LISP SDKs for 2007 are no longer available for download. See also Autodesk References External links Category:Autodesk Category:Autodesk softwareRetrospective comparison of platelet functions during non-cardiogenic pulmonary oedema in septic shock: No reduction of platelet reactivity. In patients with septic shock, thrombocytopenia is an important indicator for poor outcome. In contrast, platelet dysfunction might be associated with increased morbidity and mortality. The aim of this study was to investigate platelet function during non-cardiogenic pulmonary oedema (NCPO) in septic shock. The platelet number (PLT) and platelet function were assessed in 35 septic shock patients with NCPO (≥1.5 kPa), and in 40 septic shock patients without NCPO (NC), and in 17 patients without shock (no shock) during pulmonary oedema (NO). In patients with NCPO, there were no differences in platelet number (PLT), or in platelet function between severe/moderate shock and septic shock, or between patients with and without NCPO. Interestingly, platelet reactivity to several platelet agonists in patients with NCPO (TOF, TRAP, AA, or collagen) was significantly higher compared to the NO and NC groups. Platelet reactivity in NCPO was highest in patients without shock or severe/moderate shock, respectively. However, platelet reactivity to TOF and AA in patients with NCPO was significantly reduced compared to NO. Platelet aggregation of TOF and TRAP was significantly lower in patients with NCPO compared to NO and NC. PLT number and platelet function were not reduced in patients with NCPO, indicating that there is no "sublethal"-platelet dysfunction during NCPO. However, a higher platelet reactivity might indicate a thrombocytotoxic effect of NCPO. Platelet aggregation e315de8065
[The prevalence of HBV infection in patients with alcohol-induced liver disease in Japan]. The prevalence of HBV infection in patients with alcoholic liver disease was evaluated in our clinic. In all 14 patients with alcoholic liver disease, the serum HBsAg was negative and the serum HBeAg was positive in 8 of them. The positivity of HBsAg or HBeAg was found in 20.6% (22/104) of the patients with primary biliary cirrhosis, 15.3% (4/26) of the patients with chronic persistent hepatitis, 4.7% (1/21) of the patients with alcoholic hepatitis, 5.7% (1/17) of the patients with liver cirrhosis. The prevalence of HBsAg or HBeAg in the patients with alcoholic liver disease was significantly higher than that of the patients with primary biliary cirrhosis (p less than 0.05, p less than 0.02) or chronic persistent hepatitis (p less than 0.001). The positivity of HBsAg was in relation to the duration of drinking. The patients with chronic alcohol abuse showed a higher prevalence of the positivity than the patients with chronic alcoholism (chi 2 test; p less than 0.05). The HBeAg titers in the patients with alcoholic liver disease were higher than those in the patients with primary biliary cirrhosis (p less than 0.05), but were lower than those in the patients with chronic persistent hepatitis. These results suggest that the patients with alcoholic liver disease might be at risk of developing chronic HBV infection and the progression of the disease.[Serologic markers of Chlamydia trachomatis infection in patients with non-gonococcal urethritis]. Chlamydia trachomatis is a gram-negative intracellular pathogen which colonizes the mucosal surface of the urogenital tract. C. trachomatis is the most common bacterial cause of nongonococcal urethritis. The aim of this study was to determine serologic markers of C. trachomatis in serum of patients with nongonococcal urethritis. One hundred and forty-one samples of serum from hospitalized patients were tested for the presence of IgG and IgM specific anti-C. trachomatis antibodies by EIA. All sera were also tested for other important sexually transmitted agents including T. vaginalis, N. gonorrhoeae and V. vul
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