267 research outputs found

    Evidence-based approach to thrombophilia testing

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    Thrombophilia can be identified in about half of all patients presenting with VTE. Testing has increased tremendously for various indications, but whether the results of such tests help in the clinical management of patients has not been settled. I use evidence from observational studies to conclude that testing for hereditary thrombophilia generally does not alter the clinical management of patients with VTE, with occasional exceptions for women at fertile age. Because testing for thrombophilia only serves limited purpose this should not be performed on a routine basis

    Role of Steps in N

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    Using adsorption experiments and density functional calculations we show that N-2 dissociation on the Ru(0001) surface is totally dominated by steps. The measured adsorption rate at the steps is at least 9 orders of magnitude higher than on the terraces at 500 K, and the corresponding calculated difference in activation energy is 1.5 eV. The low barrier at the step is shown to be due to a combination of electronic and geometrical effects. The consequences for Ru as a catalyst for ammonia synthesis are discussed

    New Families with Factor XII Deficiency

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    Inherited Antithrombin Deficiency Causing Thrombophilia

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    Inherited Fibrinogen Abnormality Causing Thrombophilia

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    Factor XII Defect and Hemorrhage Evidence for a New Type of Hereditary Hemostatic Disorder

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