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Increased plasma-levels of molecular markers of coagulation activation and secondary fibrinolysis in peripheral arterial occlusive disease
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HAPTOGLOBIN POLYMORPHISM AND COMPLICATIONS IN ESTABLISHED ESSENTIAL ARTERIAL-HYPERTENSION.
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Prothrombin activation fragment 1+2, thrombin-antithrombin III complex and D-dimer determinations in peripheral arterial occlusive disease - influence of treadmill exercise.
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Haptoglobin 2-2, a genetic marker for therapy resistance in established essential hypertension
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The relation between haptoglobin polymorphism and therapeutic needs in essential arterial hypertension.
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Haptoglobin 2-2, a genetic marker for therapy resistance in established essential hypertension. Eur. Heart J., 1992, 13 (Abstract Supplement), p. 85.
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Haptoglobin phenotype 2-2: agenetic marker for therapy - resistant essential hypertension
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Basal fibrinolysis in essential hypertension and peripheral arterial disease
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Activation of the clotting cascade in peripheral arterial occlusive disease. Abstract of the 12th International Congress on Thrombosis
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Fibrinolytische parameters tijdens coronaire angioplastiek