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KOHLSCHUTTER A
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ZOLLER B
NORLUND L
LEKSELL H
NILSSON JE
VONSCHENCK H
ROSEN U
JEPSSON JO
DAHLBACK B
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Authors:
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ROSEN S
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RABE F
ZOLLER B
DAHLBACK B
Citation: Ne. Andersson et al., METHODOLOGICAL CONSIDERATIONS ON THE DETERMINATION OF THE APC RESPONSE IN PLASMA, Infusionstherapie und Transfusionsmedizin, 22, 1995, pp. 80-82
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Citation: B. Zoller et al., RESISTANCE TO ACTIVATED PROTEIN-C AS AN ADDITIONAL RISK FACTOR IN HEREDITARY-DEFICIENCY OF PROTEINS, Thrombosis and haemostasis, 73(6), 1995, pp. 1360-1360
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Citation: B. Zoller et al., HOMOZYGOUS APC-RESISTANCE COMBINED WITH INHERITED TYPE-I PROTEIN-S DEFICIENCY IN A YOUNG BOY WITH SEVERE THROMBOTIC DISEASE, Thrombosis and haemostasis, 73(5), 1995, pp. 743-745
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Authors:
ZOLLER B
BERNTSDOTTER A
DEFRUTOS PG
DAHLBACK B
Citation: B. Zoller et al., RESISTANCE TO ACTIVATED PROTEIN-C AS AN ADDITIONAL GENETIC RISK FACTOR IN HEREDITARY-DEFICIENCY OF PROTEIN-S, Blood, 85(12), 1995, pp. 3518-3523
Citation: B. Zoller et al., EVALUATION OF THE RELATIONSHIP BETWEEN PROTEIN-S AND C4B-BINDING PROTEIN ISOFORMS IN HEREDITARY PROTEIN-S DEFICIENCY DEMONSTRATING TYPE-I AND TYPE-III DEFICIENCIES TO BE PHENOTYPIC VARIANTS OF THE SAME GENETIC-DISEASE, Blood, 85(12), 1995, pp. 3524-3531
Citation: B. Zoller et B. Dahlback, LINKAGE BETWEEN INHERITED RESISTANCE TO ACTIVATED PROTEIN-C AND FACTOR-V GENE MUTATION IN VENOUS THROMBOSIS, Lancet, 343(8912), 1994, pp. 1536-1538
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Authors:
DEFRUTOS PG
ALIM RIM
HARDIG Y
ZOLLER B
DAHLBACK B
Citation: Pg. Defrutos et al., DIFFERENTIAL REGULATION OF ALPHA-CHAIN AND BETA-CHAIN OF C4B-BINDING PROTEIN DURING ACUTE-PHASE RESPONSE RESULTING IN STABLE PLASMA-LEVELS OF FREE ANTICOAGULANT PROTEIN-S, Blood, 84(3), 1994, pp. 815-822
Citation: A. Thern et al., THE LACK OF COMPLEXES BETWEEN PROTEIN-S AND C4B-BINDING PROTEIN IN BOVINE PLASMA IS EXPLAINED BY THE PRIMARY STRUCTURE OF THE BETA-CHAIN OFBOVINE C4B-BINDING PROTEIN, Thrombosis and haemostasis, 69(6), 1993, pp. 932-932
Citation: B. Zoller et B. Dahlback, PROTEIN-S DEFICIENCY IN A LARGE FAMILY WITH THROMBOPHILIA PREVIOUSLY CHARACTERIZED AS HAVING AN INHERITED FIBRINOLYTIC DEFECT, Thrombosis and haemostasis, 69(6), 1993, pp. 1256-1256