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  • 1985-1989  (2)
  • AMS(MOS): Primary 65k10  (1)
  • Diabetes mellitus  (1)
  • Nuclear reactions
Material
Years
  • 1985-1989  (2)
Year
Keywords
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Numerische Mathematik 51 (1987), S. 181-197 
    ISSN: 0945-3245
    Keywords: AMS(MOS): Primary 65k10 ; 49A10 ; 49D99 ; Secondary 73G05 ; CR: G1.6
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics
    Notes: Summary A numerical method for computing minimizers in one-dimensional problems of the calculus of variations is described. Such minimizers may have unbounded derivatives, even when the integrand is smooth and regular. In such cases, because of the Lavrentiev phenomenon, standard finite element methods may fail to converge to a minimizer. The scheme proposed is shown to converge to an absolute minimizer and is tested on an example. The effect of quadrature is analyzed. The implications for higher-dimensional problems, and in particular for fracture in nonlinear elasticity, are discussed.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-0428
    Keywords: Diabetes mellitus ; factor VIII ; ketoacidosis ; endothelial damage ; factor VIII multimers
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Factor VIII-related antigen and von Willebrand factor are synthesised by and released from vascular endothelium. Acute increases in the plasma concentration of these proteins may reflect endothelial cell damage. We have thus measured the plasma concentration of factor VIII-related antigen and von Willebrand factor, together with procoagulant factor VIII, during the course of acute diabetic ketoacidosis in seven patients. In addition, evidence for qualitative changes in the factor VIII complex was sought. Plasma factor VIII-related antigen and von Willebrand factor were markedly increased (plasma factor VIII-related antigen at presentation, median 2.75 U/ml; von Willebrand factor 2.95 U/ml) and returned toward normal with clinical and biochemical resolution (plasma factor VIII-related antigen at clinical recovery, median 1.80 U/ml; von Willebrand factor 2.05 U/ml). Plasma procoagulant factor VIII followed a similar pattern, but levels were less elevated (plasma procoagulant factor VIII, at presentation, median 1.6U/ml; at clinical recovery, 1.2U/ml). Crossed immunoelectrophoresis and sodium dodecyl sulphate-acrylamide electrophoresis with autoradiographic identification of multimeric structure revealed no evidence of structurally abnormal factor VIII-related antigen in diabetic ketoacidosis. However, an extra peak on crossed immunoelectrophoresis (“pre-peak”) was a feature in the acute phase ketoacidotic plasma in six subjects, and may represent aggregated factor VIII. Changes in plasma factor VIII are a feature of diabetic ketoacidosis and, whilst not specific to this condition, may be the result of endothelial cell damage.
    Type of Medium: Electronic Resource
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