Zobrazeno 1 - 10
of 220
pro vyhledávání: '"Loeliger, Ea"'
Autor:
Loeliger Ea
Publikováno v:
Annals of hematology. 64(2)
Careful scrutiny of relevant thrombosis prevention studies in the light of recent knowledge on the responsiveness to the anticoagulant defect of the various prothrombin time assays used in these studies casts serious doubts on the adequacy of the so-
Publikováno v:
Thrombosis and Haemostasis. 32:483-491
SummaryThe present study concerned the reproducibility of the so-called prothrombin time as assessed with a series of more commonly used modifications of the Quick’s onestage assay procedure, i.e. the British comparative reagent, homemade human bra
Publikováno v:
Thrombosis and Haemostasis. 35:289-294
SummaryTwo patients with severe factor VII deficiency appeared to be different with respect to the presence of inactive factor VH-like material in their plasma.The inactive material, demonstrated in one patient’s plasma and adsorbable onto BaSO4, i
Autor:
Loeliger Ea
Publikováno v:
Acta Haematologica. 74:125-131
Autor:
Loeliger Ea
Publikováno v:
Thrombosis and Haemostasis. 28:109-119
SummaryIt should be realized that the quality of oral anticoagulation depends on thorough pharmacological knowledge of coumarin congeners, skilled clinical supervision of the patient and well-standardized laboratory control of patients’ blood. Resu
Publikováno v:
Thrombosis and Haemostasis. :256-266
SummaryInnerfield’s method of determining antithrombin III using plasma “defibrinated” by thrombin is submitted to criticsm. This method proves to involve insufficient defibrination: the higher the fibrinogen concentration of the plasma to be t
Autor:
Loeliger Ea, Cleton Fj
Publikováno v:
Thrombosis and Haemostasis. :087-092
SummaryThe inheritance of congenital factor VII deficiency was investigated in 2 unrelated families. Out of 68 individuals, 4 (3 proven and 1 highly probable) were found to have severe factor VII deficiency (
Publikováno v:
Thrombosis and Haemostasis. 13:008-011
SummaryA case of “moderate” factor XII deficiency, with 3.6% factor XII activity, is reported. Because the activity of factor XII found in the parents of the patient is consistent with heterozygousity, the defect may be considered hereditary.
Autor:
Loeliger Ea
Publikováno v:
Acta medica Scandinavica. Supplementum. 651
Evidence in favour of oral anticoagulant therapy (OAT) in patients suffering from an acute myocardial infarction has been published in 1977 by Chalmers and co-workers (New Engl. J. Med. 297, 1091). For OAT after discharge an International Review Grou
Publikováno v:
Scandinavian journal of haematology. Supplementum. 37
The thromboplastin concept of standardization of the prothrombin-time according to Biggs and Denson survived criticism, obtained support from many countries, and recently proved to be applicable in the clinical practice of monitoring long-term oral a