Correct Hardware Design and Verification Methods: IFIP WG by Hardi Hungar, Orna Grumberg (auth.), Paolo E. Camurati, Hans

By Hardi Hungar, Orna Grumberg (auth.), Paolo E. Camurati, Hans Eveking (eds.)

This publication constitutes the refereed complaints of the IFIP WG10.5 complicated study operating convention on right layout Methodologies, CHARME '95, held in Frankfurt, Germany, in October 1995.
The 20 revised complete papers provided have been conscientiously chosen by means of this system committee and deal with all present elements of analysis and complex functions within the box of formal verification of undefined. one of the themes lined are version checking, theorem proving, officially proven synthesis, procedure algebras, finite country structures, verification environments, language containment, and VHDL.

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Extra info for Correct Hardware Design and Verification Methods: IFIP WG 10.5 Advanced Research Working Conference, CHARME '95 Frankfurt/Main, Germany, October 2–4, 1995 Proceedings

Sample text

On the other hand, fibrin is a kind of adhesive Horm Res 1998;50(suppl 2):37–45 43 Fig. 9. Adhesion system model at the implantation site. protein. It has adhesive sites for another fibrin and fibronectin. Normal plasma Fg ranges from 200 to 400 mg/dl. 5 times (35 wGF). A minimum concentration for hemostasis is 100 mg/dl. Plasma Fg half-life is 96 h. Blood coagulation factor X III is a transglutaminase which works at the final stage of blood coagulation. It is present in plasma, platelet and monocyte/macrophage.

However, in cases of special adhesive proteins, such as fibrinogen (Fg) ABC © 1998 S. com/karger and blood coagulation factor X III, congenital deficiencies and pregnancy cases are present. As to congenital afibrinogenemia, 2 cases were reported [1, 2] as summarized in table 1. Their pregnancies resulted in spontaneous abortions without any replacement therapy. Inamoto and Terao [3] reported a precise review of pregnancy cases of afibrinogenemia and hypofibrinogenemia, and also showed their own first case of delivery with replacement therapy.

In 1982 the patient became pregnant. At 5 weeks and 2 days’ gestation (5w2dG), genital bleeding occurred. She was hospitalized and 3 g of Fg was administrated. Bleeding stopped. After hospitalization, 8 g of Fg was administrated per week (8 g/w). Thereafter the administration volume decreased to 4 g/w after 9 wG, and 2 g/w after 15 wG. The patient’s plasma concentration of Fg (plasma Fg) ranged from 5 to 40 mg/dl. At 21w1dG, genital bleeding occurred, and then plasma Fg was 40 mg/dl. Thereafter, administration volume was increased to 12 g/w.

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