| Year |
Citation |
Score |
| 2014 |
Omarova F, Uitte de Willige S, Simioni P, Ariëns RA, Bertina RM, Rosing J, Castoldi E. Fibrinogen γ' increases the sensitivity to activated protein C in normal and factor V Leiden plasma. Blood. 124: 1531-8. PMID 24951429 DOI: 10.1182/Blood-2014-02-554055 |
0.554 |
|
| 2014 |
Medina P, Navarro S, Bonet E, Martos L, Estellés A, Bertina RM, Vos HL, España F. Functional analysis of two haplotypes of the human endothelial protein C receptor gene. Arteriosclerosis, Thrombosis, and Vascular Biology. 34: 684-90. PMID 24436369 DOI: 10.1161/Atvbaha.113.302518 |
0.321 |
|
| 2013 |
Omarova F, Uitte De Willige S, Ariëns RA, Rosing J, Bertina RM, Castoldi E. Inhibition of thrombin-mediated factor V activation contributes to the anticoagulant activity of fibrinogen γ'. Journal of Thrombosis and Haemostasis : Jth. 11: 1669-78. PMID 23848367 DOI: 10.1111/Jth.12354 |
0.496 |
|
| 2012 |
Bonet E, Medina P, Navarro S, Martos L, Estellés A, Bertina RM, España F. C0076 The endothelial protein C receptor is essential for protein C activation in vivo Thrombosis Research. 130: S110. DOI: 10.1016/J.Thromres.2012.08.028 |
0.345 |
|
| 2012 |
Bonet E, Navarro S, Medina P, Martos L, Ferrando F, Vayá A, Mira Y, Aznar JA, Estellés A, Bertina RM, España F. C0069 Association of haplotypes (H) 1 and 3 of the endothelial protein c receptor gene (PROCR) with venous thromboembolism Thrombosis Research. 130: S109-S110. DOI: 10.1016/J.Thromres.2012.08.027 |
0.327 |
|
| 2012 |
Martos L, Bonet E, Medina P, Navarro S, Zorio E, Rueda J, Aznar JA, Arnau MA, Osa AM, Estellés A, Bertina RM, España F. C0068 Haplotypes of the endothelial protein C receptor gene and circulating protein C levels Thrombosis Research. 130: S109. DOI: 10.1016/J.Thromres.2012.08.026 |
0.335 |
|
| 2008 |
van Vliet HA, Bertina RM, Dahm AE, Rosendaal FR, Rosing J, Sandset PM, Helmerhorst FM. Different effects of oral contraceptives containing different progestogens on protein S and tissue factor pathway inhibitor. Journal of Thrombosis and Haemostasis : Jth. 6: 346-51. PMID 18067603 DOI: 10.1111/J.1538-7836.2008.02863.X |
0.535 |
|
| 2007 |
Tchaikovski SN, van Vliet HA, Thomassen MC, Bertina RM, Rosendaal FR, Sandset PM, Helmerhorst FM, Tans G, Rosing J. Effect of oral contraceptives on thrombin generation measured via calibrated automated thrombography. Thrombosis and Haemostasis. 98: 1350-6. PMID 18064335 DOI: 10.1160/Th07-07-0439 |
0.493 |
|
| 2006 |
Tjernberg P, Castaman G, Vos HL, Bertina RM, Eikenboom JC. Homozygous C2362F von Willebrand factor induces intracellular retention of mutant von Willebrand factor resulting in autosomal recessive severe von Willebrand disease. British Journal of Haematology. 133: 409-18. PMID 16643449 DOI: 10.1111/J.1365-2141.2006.06055.X |
0.341 |
|
| 2005 |
de Visser MC, van Hylckama Vlieg A, Tans G, Rosing J, Dahm AE, Sandset PM, Rosendaal FR, Bertina RM. Determinants of the APTT- and ETP-based APC sensitivity tests. Journal of Thrombosis and Haemostasis : Jth. 3: 1488-94. PMID 15978106 DOI: 10.1111/J.1538-7836.2005.01430.X |
0.55 |
|
| 2004 |
Paffen E, Vos HL, Bertina RM. C-reactive protein does not directly induce tissue factor in human monocytes. Arteriosclerosis, Thrombosis, and Vascular Biology. 24: 975-81. PMID 15044210 DOI: 10.1161/01.Atv.0000126681.16619.69 |
0.31 |
|
| 2004 |
Guimarães AH, van Tilburg NH, Vos HL, Bertina RM, Rijken DC. Association between thrombin activatable fibrinolysis inhibitor genotype and levels in plasma: comparison of different assays. British Journal of Haematology. 124: 659-65. PMID 14871254 DOI: 10.1111/J.1365-2141.2004.04824.X |
0.31 |
|
| 2004 |
van der Neut Kolfschoten M, Dirven RJ, Vos HL, Tans G, Rosing J, Bertina RM. Factor Va is inactivated by activated protein C in the absence of cleavage sites at Arg-306, Arg-506, and Arg-679. The Journal of Biological Chemistry. 279: 6567-75. PMID 14660667 DOI: 10.1074/Jbc.M308574200 |
0.538 |
|
| 2003 |
Tans G, van Hylckama Vlieg A, Thomassen MC, Curvers J, Bertina RM, Rosing J, Rosendaal FR. Activated protein C resistance determined with a thrombin generation-based test predicts for venous thrombosis in men and women. British Journal of Haematology. 122: 465-70. PMID 12877675 DOI: 10.1046/J.1365-2141.2003.04443.X |
0.515 |
|
| 2002 |
Van Hylckama Vlieg A, Komanasin N, Ariëns RA, Poort SR, Grant PJ, Bertina RM, Rosendaal FR. Factor XIII Val34Leu polymorphism, factor XIII antigen levels and activity and the risk of deep venous thrombosis. British Journal of Haematology. 119: 169-75. PMID 12358922 DOI: 10.1046/J.1365-2141.2002.03797.X |
0.319 |
|
| 2002 |
van der Neut Kolfschoten M, Dirven RJ, Tans G, Rosing J, Vos HL, Bertina RM. The activated protein C (APC)-resistant phenotype of APC cleavage site mutants of recombinant factor V in a reconstituted plasma model. Blood Coagulation & Fibrinolysis : An International Journal in Haemostasis and Thrombosis. 13: 207-15. PMID 11943934 DOI: 10.1097/00001721-200204000-00006 |
0.503 |
|
| 2002 |
Curvers J, Christella M, Thomassen LG, de Ronde H, Bertina RM, Rosendaal FR, Tans G, Rosing J. Effects of (pre-)analytical variables on activated protein C resistance determined via a thrombin generation-based assay. Thrombosis and Haemostasis. 87: 483-92. PMID 11924538 DOI: 10.1055/S-0037-1613029 |
0.536 |
|
| 2001 |
Høibraaten E, Mowinckel MC, de Ronde H, Bertina RM, Sandset PM. Hormone replacement therapy and acquired resistance to activated protein C: results of a randomized, double-blind, placebo-controlled trial. British Journal of Haematology. 115: 415-20. PMID 11703344 DOI: 10.1046/J.1365-2141.2001.03111.X |
0.363 |
|
| 2001 |
Lensen R, Bertina RM, Vandenbroucke JP, Rosendaal FR. High factor VIII levels contribute to the thrombotic risk in families with factor V Leiden. British Journal of Haematology. 114: 380-6. PMID 11529860 DOI: 10.1046/J.1365-2141.2001.02946.X |
0.356 |
|
| 1998 |
Van Wijnen M, Van 't Veer C, Meijers JCM, Bertina RM, Bouma BN. A plasma coagulation assay for an activated protein C-independent anticoagulant activity of protein S Thrombosis and Haemostasis. 80: 930-935. PMID 9869163 DOI: 10.1055/S-0037-1615391 |
0.428 |
|
| 1998 |
Fernández JA, Griffin JH, Chang GTG, Stam J, Reitsma PH, Bertina RM, Bouma BN. Involvement of amino acid residues 423-429 of human protein S in binding to C4b-binding protein Blood Cells, Molecules and Diseases. 24: 101-113. PMID 9628846 DOI: 10.1006/Bcmd.1998.0175 |
0.349 |
|
| 1998 |
Doggen CJM, Cats VM, Bertina RM, Rosendaal FR. Interaction of coagulation defects and cardiovascular risk factors: Increased risk of myocardial infarction associated with factor V Leiden or prothrombin 20210A Circulation. 97: 1037-1041. PMID 9531249 DOI: 10.1161/01.Cir.97.11.1037 |
0.308 |
|
| 1998 |
Van Wijnen M, Stam JG, Chang GTG, Meijers JCM, Reitsma PH, Bertina RM, Bouma BN. Characterization of mini-protein S, a recombinant variant of protein S that lacks the sex hormone binding globulin-like domain Biochemical Journal. 330: 389-396. PMID 9461535 DOI: 10.1042/Bj3300389 |
0.405 |
|
| 1997 |
Bernardi F, Arcieri P, Bertina RM, Chiarotti F, Corral J, Pinotti M, Prydz H, Samama M, Sandset PM, Strom R, Vicente Garcia V, Mariani G. Contribution of factor VII genotype to activated FVII levels: Differences in genotype frequencies between northern and southern European populations Arteriosclerosis, Thrombosis, and Vascular Biology. 17: 2548-2553. PMID 9409226 DOI: 10.1161/01.Atv.17.11.2548 |
0.306 |
|
| 1997 |
Van 'T Veer C, Golden NJ, Kalafatis M, Simioni P, Bertina RM, Mann KG. An in vitro analysis of the combination of hemophilia A and factor V(LEIDEN) Blood. 90: 3067-3072. PMID 9376587 DOI: 10.1182/Blood.V90.8.3067 |
0.397 |
|
| 1997 |
Van 't Veer C, Kalafatis M, Bertina RM, Simioni P, Mann KG. Increased tissue factor-initiated prothrombin activation as a result of the Arg506 → Gln mutation in factor V(LEIDEN) Journal of Biological Chemistry. 272: 20721-20729. PMID 9252393 DOI: 10.1074/Jbc.272.33.20721 |
0.338 |
|
| 1997 |
Haan J, Kappelle LJ, De Ronde H, Ferrari MD, Bertina RM. The factor V leiden mutation (R506Q) is not a major risk factor for migrainous cerebral infarction Cephalalgia. 17: 605-607. PMID 9251878 DOI: 10.1046/J.1468-2982.1997.1705605.X |
0.342 |
|
| 1996 |
Poort SR, Rosendaal FR, Reitsma PH, Bertina RM. A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis Blood. 88: 3698-3703. PMID 8916933 DOI: 10.1182/Blood.V88.10.3698.Bloodjournal88103698 |
0.326 |
|
| 1996 |
Van Wijnen M, Stam JG, Van't Veer C, Meijers JCM, Reitsma PH, Bertina RM, Bouma BN. The interaction of protein S with the phospholipid surface is essential for the activated protein C-independent activity of protein S Thrombosis and Haemostasis. 76: 397-403. PMID 8883277 DOI: 10.1055/S-0038-1650590 |
0.393 |
|
| 1996 |
Holmes ZR, Bertina RM, Reitsma PH. Characterization of a large chromosomal deletion in the PROS1 gene of a patient with protein S deficiency type I using long PCR British Journal of Haematology. 92: 986-991. PMID 8616098 DOI: 10.1046/J.1365-2141.1996.403943.X |
0.304 |
|
| 1995 |
Spek CA, Koster T, Rosendaal FR, Bertina RM, Reitsma PH. Genotypic variation in the promoter region of the protein C gene is associated with plasma protein C levels and thrombotic risk. Arteriosclerosis, Thrombosis, and Vascular Biology. 15: 214-8. PMID 7749828 DOI: 10.1161/01.ATV.15.2.214 |
0.306 |
|
| 1995 |
Kalafatis M, Lu D, Bertina RM, Long GL, Mann KG. Biochemical prototype for familial thrombosis. A study combining a functional protein C mutation and factor V Leiden. Arteriosclerosis, Thrombosis, and Vascular Biology. 15: 2181-7. PMID 7489240 DOI: 10.1161/01.Atv.15.12.2181 |
0.307 |
|
| 1995 |
Gomez E, Poort SR, Bertina RM, Reitsma PH. Identification of eight point mutations in protein S deficiency type I: Analysis of 15 pedigrees Thrombosis and Haemostasis. 73: 750-755. PMID 7482398 DOI: 10.1055/S-0038-1653863 |
0.361 |
|
| 1994 |
Bertina RM, Koeleman BP, Koster T, Rosendaal FR, Dirven RJ, de Ronde H, van der Velden PA, Reitsma PH. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature. 369: 64-7. PMID 8164741 DOI: 10.1038/369064a0 |
0.344 |
|
| 1994 |
Poort SR, Michiels JJ, Reitsma PH, Bertina RM. Homozygosity for a Novel Missense Mutation in the Prothrombin Gene Causing a Severe Bleeding Disorder Thrombosis and Haemostasis. 72: 819-824. DOI: 10.1055/S-0038-1648968 |
0.323 |
|
| 1994 |
Chang GTG, Aaldering L, Hackeng TM, Reitsma PH, Bertina RM, Bouma BN. Construction and Characterization of Thrombin-resistant Variants of Recombinant Human Protein S Thrombosis and Haemostasis. 72: 693-697. DOI: 10.1055/S-0038-1648944 |
0.405 |
|
| 1994 |
Chang GTG, Maas BHA, Amstel HKPv, Reitsma PH, Bertina RM, Bouma BN. Studies of the Interaction between Human Protein S and Human C4b-Binding Protein Using Deletion Variants of Recombinant Human Protein S Thrombosis and Haemostasis. 71: 461-467. DOI: 10.1055/S-0038-1642461 |
0.398 |
|
| 1993 |
Bakker HM, Tans G, Yukelson LY, Janssen-Claessen TW, Bertina RM, Hemker HC, Rosing J. Protein C activation by an activator purified from the venom of Agkistrodon halys halys Blood Coagulation and Fibrinolysis. 4: 605-614. PMID 8218858 DOI: 10.1097/00001721-199308000-00012 |
0.631 |
|
| 1993 |
Koster T, Vandenbroucke J, Rosendaal F, Ronde Hd, Briët E, Bertina R. Venous thrombosis due to poor anticoagulant response to activated protein C: Leiden Thrombophilia Study The Lancet. 342: 1503-1506. PMID 7902898 DOI: 10.1016/S0140-6736(05)80081-9 |
0.311 |
|
| 1993 |
Boyer-Neumann C, Bertina RM, Tripodi A, D'Angelo A, Wolf M, D'Angelo SV, Mannucci PM, Meyer D, Larrieu MJ. Comparison of Functional Assays for Protein S: European Collaborative Study of Patients with Congenital and Acquired Deficiency Thrombosis and Haemostasis. 70: 0946-0950. DOI: 10.1055/S-0038-1649705 |
0.396 |
|
| 1992 |
Conard J, Horellou MH, van Dreden P, Samama M, Reitsma PH, Poort S, Bertina RM. Homozygous protein C deficiency with late onset and recurrent coumarin-induced skin necrosis. Lancet (London, England). 339: 743-4. PMID 1347608 DOI: 10.1016/0140-6736(92)90641-F |
0.322 |
|
| 1992 |
Chang GTG, Ploos van Amstel HK, Hessing M, Reitsma PH, Bertina RM, Bouma BN. Expression and Characterization of Recombinant Human Protein S in Heterologous Cells - Studies of the Interaction of Amino Acid Residues Leu-608 to Glu-612 with Human C4b-Binding Protein Thrombosis and Haemostasis. 67: 526-532. DOI: 10.1055/S-0038-1648487 |
0.394 |
|
| 1991 |
Reitsma P, Poort S, Allaart C, Briet E, Bertina R. The spectrum of genetic defects in a panel of 40 Dutch families with symptomatic protein C deficiency type I: heterogeneity and founder effects Blood. 78: 890-894. DOI: 10.1182/Blood.V78.4.890.Bloodjournal784890 |
0.377 |
|
| 1990 |
Deutz-Terlouw PP, Ballering L, van Wijngaarden A, Bertina RM. Two ELISA's for measurement of protein S, and their use in the laboratory diagnosis of protein S deficiency. Clinica Chimica Acta; International Journal of Clinical Chemistry. 186: 321-34. PMID 2138066 DOI: 10.1016/0009-8981(90)90318-M |
0.389 |
|
| 1990 |
Poort SR, Briët E, Bertina RM, Reitsma PH. Two Mutations of the Factor IX Gene Including a Donor Splice Consensus Deletion and a Point Mutation in a Dutch Patient with Severe Hemophilia B Thrombosis and Haemostasis. 64: 379-384. DOI: 10.1055/S-0038-1647323 |
0.301 |
|
| 1990 |
Allaart CF, Aronson DC, Ruys T, Rosendaal FR, van Bockel JH, Bertina RM, Briët E. Hereditary Protein S Deficiency in Young Adults with Arterial Occlusive Disease Thrombosis and Haemostasis. 64: 206-210. DOI: 10.1055/S-0038-1647286 |
0.369 |
|
| 1990 |
Bom VJJ, Reinalda-Poot JH, Cupers R, Bertina RM. Extrinsic Activation of Human Blood Coagulation Factors IX and X Thrombosis and Haemostasis. 63: 224-230. DOI: 10.1055/S-0038-1645199 |
0.356 |
|
| 1989 |
Reitsma P, Mandalaki T, Kasper C, Bertina R, Briet E. Two novel point mutations correlate with an altered developmental expression of blood coagulation factor IX (hemophilia B Leyden phenotype) Blood. 73: 743-746. DOI: 10.1182/Blood.V73.3.743.Bloodjournal733743 |
0.332 |
|
| 1989 |
Ploos van Amstel H, Huisman M, Reitsma P, Wouter ten Cate J, Bertina R. Partial protein S gene deletion in a family with hereditary thrombophilia Blood. 73: 479-483. DOI: 10.1182/Blood.V73.2.479.Bloodjournal732479 |
0.359 |
|
| 1988 |
Poort SR, Deutz-Terlouw PP, van Wijngaarden A, Bertina RM. Immunoradiometric assays for the Ca(II)-dependent and Ca(II)-independent conformation of human protein C. Thrombosis Research. 52: 87-100. PMID 3194894 DOI: 10.1016/0049-3848(88)90087-4 |
0.313 |
|
| 1988 |
Reitsma P, Bertina R, Ploos van Amstel J, Riemens A, Briet E. The putative factor IX gene promoter in hemophilia B Leyden Blood. 72: 1074-1076. DOI: 10.1182/Blood.V72.3.1074.Bloodjournal7231074 |
0.329 |
|
| 1987 |
Bom VJ, Reinalda-Poot HH, Poort SR, Cupers R, Bertina RM. Solid phase immunoradiometric assay of activated human coagulation factor IX. Thrombosis Research. 45: 661-7. PMID 3495901 DOI: 10.1016/0049-3848(87)90328-8 |
0.354 |
|
| 1987 |
Broekmans AW, van Rooyen W, Westerveld BD, Briët E, Bertina RM. Mesenteric vein thrombosis as presenting manifestation of hereditary protein S deficiency. Gastroenterology. 92: 240-2. PMID 2946623 DOI: 10.1016/0016-5085(87)90867-5 |
0.38 |
|
| 1987 |
Broekmans AW, Conard J, van Weyenberg RG, Horellou MH, Kluft C, Bertina RM. Treatment of Hereditary Protein C Deficiency with Stanozolol Thrombosis and Haemostasis. 57: 020-024. DOI: 10.1055/S-0038-1651054 |
0.453 |
|
| 1987 |
Poort SR, Deutz-Terlouw PP, van Wijngaarden A, Bertina RM. Immunoradiometric Assay for the Calcium-Stabilized Conformation of Human Protein S Thrombosis and Haemostasis. 58: 0998-1004. DOI: 10.1055/S-0038-1646044 |
0.326 |
|
| 1986 |
Bom VJ, Ram IE, Alderkamp GH, Reinalda-Poot HH, Bertina RM. Application of factor VII-Sepharose affinity chromatography in the purification of human tissue factor apoprotein. Thrombosis Research. 42: 635-43. PMID 3715822 DOI: 10.1016/0049-3848(86)90342-7 |
0.352 |
|
| 1986 |
Bom VJJ, van Tilburg NH, Es CK, Bertina RM. Immunoradiometric Assays for Human Coagulation Factor VII Using Polyclonal Antibodies Against the Ca(II)-Dependent and Ca(II)-Independent Conformation Thrombosis and Haemostasis. 56: 343-348. DOI: 10.1055/S-0038-1666778 |
0.365 |
|
| 1986 |
Poort SR, Linden IKvd, Es CK, Briët E, Bertina RM. Rabbit Polyclonal Antibodies Against the Calcium-Dependent Conformation of Factor IX and Their Application in Solid Phase Immunoradiometric Assays Thrombosis and Haemostasis. 55: 122-128. DOI: 10.1055/S-0038-1661461 |
0.324 |
|
| 1986 |
Michiels J, Bertina R, Broekmans A. Effectiveness of longterm oral anticoagulant treatment in preventing thrombosis in hereditary protein S deficiency Thrombosis Research. 41: 136. DOI: 10.1016/0049-3848(86)91617-8 |
0.331 |
|
| 1985 |
Conard J, Horellou MH, Teger-Nilsson AC, Bertina RM, Samama M. The fibrinolytic system in patients with congenital protein C deficiency. Thrombosis Research. 36: 363-7. PMID 6549234 DOI: 10.1016/0049-3848(84)90328-1 |
0.354 |
|
| 1985 |
Klingemann HG, Broekmans AW, Bertina RM, Egbring R, Loeliger EA. [Protein C deficiency--a risk factor for venous thrombosis]. Klinische Wochenschrift. 62: 975-8. PMID 6548780 DOI: 10.1007/Bf01728427 |
0.432 |
|
| 1985 |
Bertina RM, Cupers R, van Wijngaarden A. Factor IXa protects activated factor VIII against inactivation by activated protein C. Biochemical and Biophysical Research Communications. 125: 177-83. PMID 6439201 DOI: 10.1016/S0006-291X(84)80351-4 |
0.417 |
|
| 1985 |
Bertina RM. Hereditary protein S deficiency. Haemostasis. 15: 241-6. PMID 2931333 DOI: 10.1159/000215155 |
0.327 |
|
| 1985 |
Broekmans AW, Bertina RM, Reinalda-Poot J, Engesser L, Muller HP, Leeuw JA, Michiels JJ, Brommer EJP, Briët E. Hereditary Protein S Deficiency and Venous Thrombo-Embolism Thrombosis and Haemostasis. 53: 273-277. DOI: 10.1055/S-0038-1661292 |
0.362 |
|
| 1985 |
Bertina RM, van Wijngaarden A, Reinalda-Poot J, Poort SR, Bom VJJ. Determination of Plasma Protein S - The Protein Cofactor of Activated Protein C Thrombosis and Haemostasis. 53: 268-272. DOI: 10.1055/S-0038-1661291 |
0.404 |
|
| 1985 |
Mertens K, van Wijngaarden A, Bertina RM. The Role of Factor VIII in the Activation of Human Blood Coagulation Factor X by Activated Factor IX Thrombosis and Haemostasis. 54: 654-660. DOI: 10.1055/S-0038-1660091 |
0.35 |
|
| 1985 |
Mertens K, van Wijngaarden A, Bertina RM, Veltkamp JJ. The Functional Defect of Factor VIII Leiden, a Genetic Variant of Coagulation Factor VIII Thrombosis and Haemostasis. 54: 650-653. DOI: 10.1055/S-0038-1660090 |
0.376 |
|
| 1985 |
Blamey SL, Lowe GDO, Bertina RM, Kluft C, Sue-Ling HM, Davies JA, Forbes CD. Protein C Antigen Levels in Major Abdominal Surgery: Relationships to Deep Vein Thrombosis, Malignancy and Treatment with Stanozolol Thrombosis and Haemostasis. 54: 622-625. DOI: 10.1055/S-0038-1660084 |
0.354 |
|
| 1984 |
Kluft C, Bertina RM, Preston FE, Malia RG, Blamey SL, Lowe GD, Forbes CD. Protein C, an anticoagulant protein, is increased in healthy volunteers and surgical patients after treatment with stanozolol. Thrombosis Research. 33: 297-304. PMID 6546815 DOI: 10.1016/0049-3848(84)90165-8 |
0.37 |
|
| 1984 |
Brommer EJ, Kluft C, Bertina RM, Alderkamp GH. Effect of DDAVP on plasma levels of factor VII and XII. British Journal of Haematology. 57: 173-5. PMID 6426497 DOI: 10.1111/J.1365-2141.1984.Tb02878.X |
0.331 |
|
| 1984 |
Kluft C, Preston FE, Malia RG, Bertina RM, Wijngaards G, Greaves M, Verheijen JH, Dooijewaard G. Stanozolol-Induced Changes in Fibrinolysis and Coagulation in Healthy Adults Thrombosis and Haemostasis. 51: 157-164. DOI: 10.1055/S-0038-1661049 |
0.356 |
|
| 1984 |
Bertina RM, Broekmans AW, Es CK, Wijngaarden Av. The Use of a Functional and Immunologic Assay for Plasma Protein C in the Study of the Heterogeneity of Congenital Protein C Deficiency Thrombosis and Haemostasis. 51: 001-005. DOI: 10.1055/S-0038-1660995 |
0.415 |
|
| 1983 |
Broekmans AW, Veltkamp JJ, Bertina RM. Congenital protein C deficiency and venous thromboembolism. A study of three Dutch families. The New England Journal of Medicine. 309: 340-4. PMID 6688122 DOI: 10.1056/NEJM198308113090604 |
0.308 |
|
| 1983 |
Pabinger-Fasching I, Bertina RM, Lechner K, Niessner H, Korninger C. Protein C Deficiency in Two Austrian Families Thrombosis and Haemostasis. 50: 810-813. DOI: 10.1055/S-0038-1665318 |
0.378 |
|
| 1982 |
Mertens K, Wortelboer M, van Dieijen G, Bertina RM. Proteolysis of blood coagulation factor X by activated factor X: difference between the bovine and human proteins. Febs Letters. 139: 174-6. PMID 7075771 DOI: 10.1016/0014-5793(82)80844-2 |
0.357 |
|
| 1982 |
van den Besselaar AMHP, Ram IE, Alderkamp GHJ, Bertina RM. The Role of Factor IX in Tissue Thromboplastin Induced Coagulation Thrombosis and Haemostasis. 48: 054-058. DOI: 10.1055/S-0038-1657215 |
0.384 |
|
| 1982 |
Bertina RM, Broekmans AW, van der Linden IK, Mertens K. Protein C Deficiency in a Dutch Family with Thrombotic Disease Thrombosis and Haemostasis. 48: 001-005. DOI: 10.1055/S-0038-1657202 |
0.408 |
|
| 1982 |
Bertina RM. More Than One Type of Factor X in Plasma of Patients Using Oral Anticoagulants Thrombosis and Haemostasis. 47: 187-187. DOI: 10.1055/S-0038-1657161 |
0.328 |
|
| 1982 |
Bertina RM, Linden IKvd. Factor IX Deventer-Evidence for the Heterogeneity of Hemophilia BM Thrombosis and Haemostasis. 47: 136-140. DOI: 10.1055/S-0038-1657148 |
0.357 |
|
| 1982 |
Mertens K, Bertina RM. Activation of Human Coagulation Factor VIII by Activated Factor X, the Common Product of the Intrinsic and the Extrinsic Pathway of Blood Coagulation Thrombosis and Haemostasis. 47: 096-100. DOI: 10.1055/S-0038-1657137 |
0.351 |
|
| 1981 |
Terwiel J, Veltkamp JJ, Bertina RM, Muller HP. Coagulation factors in the human fetus of about 20 weeks of gestational age. British Journal of Haematology. 45: 641-50. PMID 7426442 DOI: 10.1111/J.1365-2141.1980.Tb07187.X |
0.352 |
|
| 1981 |
Bertina RM, Westhoek-Kuipers MEJ, Alderkamp GHJ. The Inhibitor of Prothrombin Conversion in Plasma of Patients on Oral Anticoagulant Treatment Thrombosis and Haemostasis. 45: 237-241. DOI: 10.1055/S-0038-1650178 |
0.363 |
|
| 1975 |
Bertina RM, Slater EC. The effects of phosphate and electron transport on the carbonyl cyanide m-chlorophenylhydrazone-induced ATPase of rat-liver mitochondria. Biochimica Et Biophysica Acta. 376: 492-504. PMID 123770 DOI: 10.1016/0005-2728(75)90170-X |
0.438 |
|
| 1974 |
Bertina RM, Steenstra JA, Slater EC. The mechanism of inhibition by oligomycin of oxidative phosphorylation in mitochondria. Biochimica Et Biophysica Acta. 368: 279-97. PMID 4451653 DOI: 10.1016/0005-2728(74)90175-3 |
0.39 |
|
| 1973 |
Bertina RM, Schrier PI, Slater EC. The binding of aurovertin to mitochondria, and its effect on mitochondrial respiration. Biochimica Et Biophysica Acta. 305: 503-18. PMID 4270153 DOI: 10.1016/0005-2728(73)90072-8 |
0.402 |
|
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