Results 191 to 200 of about 22,631 (237)
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Antithrombin III deficiency

Blood Reviews, 1988
A moderate reduction of plasma antithrombin activity is an uncommon but clinically important cause of severe thromboembolic disease. In recent years the molecule responsible for the major part of this activity (antithrombin III) has been extensively characterised and the mode of inheritance of familial deficiencies worked out.
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Antithrombin III Concentrates

Hematology/Oncology Clinics of North America, 1992
The general characteristics of antithrombin III (AT III) concentrates available in the United States are described in this article. The effectiveness of AT III concentrates in the prevention and treatment of thrombotic episodes in patients with hereditary AT III deficiency are summarized, and the use of this product in various conditions with acquired ...
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Abnormal Antithrombin III (Antithrombin III ‘Budapest’) as a Cause of a Familial Thrombophilia

Thrombosis and Haemostasis, 1974
SummaryA family with a high incidence of spontaneous thromboembolism has been investigated and those members affected were found to have significantly depressed levels of plasma and serum heparin cofactor activity; i.e., antithrombin III and anti-Xa activity.
G, Sas   +4 more
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Antithrombin III concentrate: its catabolism in health and in antithrombin III deficiency

Scandinavian Journal of Clinical and Laboratory Investigation, 1981
The catabolism of purified radiolabelled antithrombin III (AT III) concentrate was studied in two normals and two patients with congenital AT III deficiency both alone and combined with warfarin. The radiolabelling with iodine monochloride did not change the quality of the concentrate. The half-life varied between 3.4 and 4.8 days.
L, Tengborn   +3 more
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Isolation and characterization of a hereditary abnormal antithrombin III ‘antithrombin III toyama’

Thrombosis Research, 1983
A hereditary abnormal antithrombin III (AT-III) 'Antithrombin III Toyama' was purified from the plasma of a patient with recurrent thrombophlebitis by a procedure involving barium chloride and ammonium sulfate fractionations, affinity chromatography on anti-AT-III-Sepharose gel, and DEAE-Sephadex chromatography. Purified abnormal AT-III was shown to be
T, Koide   +4 more
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Microheterogeneity of Human Antithrombin III

British Journal of Haematology, 1978
Summary. Antithrombin purified from normal human plasma has been separated into two fractions by isoelectric focusing in a pH 4‐6 gradient. These fractions were homogeneous by polyacrylamide gel electrophoresis, had similar amino acid composition and the same specific activity. Both of them cross reacted with antiserum against antithrombin.
A, Borsodi, T R, Narasimhan
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Detection of antithrombin III microheterogeneity

Thrombosis Research, 1985
Antithrombin III microheterogeneity was investigated by isoelectric focusing and immunofixation in healthy individuals and in patients with clinical conditions in which antithrombin III is known to vary (liver disease, nephrotic syndrome, after surgery and anticoagulant therapy). In normal plasma microheterogeneity was present with ten bands of varying
A E, Milner   +3 more
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Antithrombin III in normal pregnancy

Thrombosis Research, 1982
Plasma antithrombin III (AT III) was determined in 94 women during and after normal pregnancy employing an automated amidolytic technique. The patients were selected on the following criteria: no toxaemia, spontaneous delivery at term, birth-weight above the 10th percentile and discharged with a healthy baby.
G H, Weenink   +3 more
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Antithrombin III

International Journal of Biochemistry, 1990
C H, Beresford, M C, Owen
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ANTITHROMBIN III AND HEPARIN

British Medical Bulletin, 1978
T W, Barrowcliffe   +2 more
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