DOI: 10.1055/s-00035024

Thrombosis and Haemostasis

Issue 10 · Volume 84 · 2000 DOI: 10.1055/s-008-36075

Commentary

  • 524
    Muszbek, L.:

    Deficiency Causing Mutations and Common Polymorphisms in the Factor XIII-A Gene

    • Review Article

  • 528
    Cines, Douglas B.; Konkle, Barbara A.; Furlan, Miha:

    Thrombotic Thrombocytopenic Purpura: A Paradigm Shift?

  • 536
    Baronciani, Luciano; Cozzi, Giovanna; Canciani, Maria Teresa; Peyvandi, Flora; Srivastava, Alok; Federici, Augusto Bramante; Mannucci, Pier Mannuccio:

    Molecular Characterization of a Multiethnic Group of 21 Patients with Type 3 von Willebrand Disease

  • 541
    Favaloro, Emmanuel J.; Henniker, Anthony; Facey, David; Hertzberg, Mark:

    Discrimination of von Willebrands Disease (VWD) Subtypes: Direct Comparison of von Willebrand Factor:Collagen Binding Assay (VWF:CBA) with Monoclonal Antibody (MAB) Based VWF-capture Systems

  • 548
    Wicki, Jacques; Perrier, Arnaud; Perneger, Thomas V.; Bounameaux, Henri; Junod, Alain François:

    Predicting Adverse Outcome in Patients with Acute Pulmonary Embolism: A Risk Score

  • 553
    Lowe, Gordon; Rumley, Ann; Norrie, John; Ford, Ian; Shepherd, James; Cobbe, Stuart; Macfarlane, Peter; Packard, Christopher; The West of Scotland Coronary Prevention Study Group; on behalf of:

    Blood Rheology, Cardiovascular Risk Factors, and Cardiovascular Disease: The West of Scotland Coronary Prevention Study

  • 559
    Veiga, F.; Escribá, A.; Maluenda, M. P.; Rubio, M. López; Margalet, I.; Lezana, A.; Gallego, J.; Ribera, J. M.:

    Low Molecular Weight Heparin (Enoxaparin) Versus Oral Anticoagulant Therapy (Acenocoumarol) in the Long-Term Treatment of Deep Venous Thrombosis in the Elderly: a Randomized Trial

  • 565
    Sechi, Leonardo A.; Zingaro, Laura; Catena, Cristiana; De Marchi, Sergio:

    Increased Fibrinogen Levels and Hemostatic Abnormalities in Patients with Arteriolar Nephrosclerosis: Association with Cardiovascular Events

  • 571
    Agewall, Stefan; Bokemark, Lena; Wikstrand, John; Lindahl, Anders; Fagerberg, Björn:

    Insulin Sensitivity and Hemostatic Factors in Clinically Healthy 58-year-old Men

  • 576
    de Franchis, Raffaella; Fermo, Isabella; Mazzola, Giuseppina; Sebastio, Gianfranco; Di Minno, Giovanni; Coppola, Antonio; Andria, Generoso; D’Angelo, Armando:

    Contribution of the Cystathionine β-Synthase Gene (844ins68) Polymorphism to the Risk of Early-onset Venous and Arterial Occlusive Disease and of Fasting Hyperhomocysteinemia

  • 583
    Maki, Masahiro; Kobayashi, Takao; Terao, Toshihiko; Ikenoue, Tsuyomu; Satoh, Kazuo; Nakabayashi, Masao; Sagara, Yusuke; Kajiwara, Yayoi; Urata, Masao; for BI51.017 Study Group:

    Antithrombin Therapy for Severe Preeclampsia

  • 591
    Anwar, Rashida; Gallivan, Louise; Miloszewski, Krzysztof J. A.; Markham, Alexander F.:

    Factor XIII Deficiency Causing Mutation, Ser295Arg, in Exon 7 of the Factor XIIIA Gene

  • 595
    Wartiovaara, U.; Mikkola, H.; Szôke, G.; Haramura, G.; Kárpáti, L.; Balogh, I.; Lassila, R.; Muszbek, L.; Palotie, A.:

    Effect of Val34Leu Polymorphism on the Activation of the Coagulation Factor XIII-A

  • 601
    Attié-Castro, Flávia A.; Zago, Marco A.; Lavinha, João; Elion, J.; Rodriguez-Delfin, L.; F.Guerreiro, João; Franco, Rendrik F.:

    Ethnic Heterogeneity of the Factor XIII Val34Leu Polymorphism

  • 604
    Morbœuf, Olivier; Borgel, Delphine; Gaussem, Pascale; Vincenot, Anne; Pittet, Jean-Louis; Aiach, Martine; Gandrille, Sophie:

    Characterization of Cleaved Plasma Protein S with a Monoclonal Antibody-based Assay

  • 611
    Vogel, Gerard M. T.; van Amsterdam, Ronald G. M.; van Dinther, Theo G.; Tromp, Marijke; Meuleman, Dirk G.:

    Pre-Clinical Pharmacological Profile of the Novel Glycoconjugate Org 36764 with both Factor Xa and Thrombin (IIa) Inhibitory Activities

  • 621
    Vanhoorelbeke, K.; van der Plas, R. M.; Vandecasteele, G.; Vauterin, S.; Huizinga, E. G.; Sixma, J. J.; Deckmyn, H.:

    Sequence Alignment between vWF and Peptides Inhibiting the vWF-collagen Interaction Does not Result in the Identification of a Collagen-binding Site in vWF

  • 626
    Wu, Pai-Chih; Hamaguchi, N.; Yu, Yi-Shing; Shen, Ming-Ching; Lin, Shu-Wha:

    Hemophilia B with Mutations at Glycine-48 of Factor IX Exhibited Delayed Activation by the Factor VIIa-tissue Factor Complex

  • 635
    Peyvandi, Flora; Mannucci, Pier M.; Jenkins, P. Vince; Lee, Anselm; Coppola, Raffaella; Perry, David J.:

    Homozygous 2bp Deletion in the Human Factor VII Gene: A Non-Lethal Mutation that Is Associated with a Complete Absence of Circulating Factor VII

  • 638
    Keularts, Irene M. L. W.; Hamulyak, K.; Hemker, H.C.; Béguin, Suzette:

    The Effect of DDAVP Infusion on Thrombin Generation in Platelet-rich Plasma of von Willebrand Type 1 and in Mild Haemophilia A Patients

  • 643
    Reding, Mark T.; Wu, Huiyun; Krampf, Mark; Okita, David K.; Diethelm-Okita, Brenda M.; Christie, Beverly A.; Key, Nigel S.; Conti-Fine, Bianca M.:

    Sensitization of CD4+ T Cells to Coagulation Factor VIII: Response in Congenital and Acquired Hemophilia Patients and in Healthy Subjects

  • 653
    Salemink, Irene; Blezer, Ron; Willems, George M.; Galli, Monica; Bevers, Edouard; Lindhout, Theo:

    Antibodies to β2-Glycoprotein I Associated with Antiphospholipid Syndrome Suppress the Inhibitory Activity of Tissue Factor Pathway Inhibitor

  • 657
    Carson, Steven D.; Bromberg, Michael E.:

    Tissue Factor Encryption/de-encryption Is not Altered in the Absence of the Cytoplasmic Domain

  • 664
    van den Besselaar, A. M. H. P.; Chantarangkul, V.; Tripodi, A.:

    A Comparison of Two Sodium Citrate Concentrations in Two Evacuated Blood Collection Systems for Prothrombin Time and ISI Determination

  • 668
    Hérault, J. P.; Perrin, B.; Jongbloet, C.; Pflieger, A. M.; Bernat, A.; Herbert, J. M.:

    Effect of Factor Xa Inhibitors on the Platelet-derived Microparticles Procoagulant Activity In Vitro> and In Vivo in Rats

  • 675
    Shigekiyo, Toshio; Yoshida, Hidemasa; Kanagawa, Yasuhiko; Satoh, Koichi; Wakabayashi, Sadao; Matsumoto, Toshio; Koide, Takehiko:

    Histidine-rich Glycoprotein (HRG) Tokushima 2: Novel HRG Deficiency, Molecular and Cellular Characterization

  • 680
    Ganné, Florence; Vasse, Marc; Beaudeux, Jean-Louis; Peynet, Jacqueline; François, Arnaud; Mishal, Zohar; Chartier, Antoine; Tobelem, Gérard; Vannier, Jean-Pierre; Soria, Jeannette; Soria, Claudine:

    Cerivastatin, an Inhibitor of HMG-CoA Reductase, Inhibits Urokinase/Urokinase-receptor Expression and MMP-9 Secretion by Peripheral Blood Monocytes

  • 689
    Michelson, Alan D.; Rajasekhar, Damodara; Bednarek, Francis J.; Barnard, Marc R.:

    Platelet and Platelet-derived Microparticle Surface Factor V/Va Binding in Whole Blood: Differences between Neonates and Adults

  • 695
    Bar, J.; Lahav, J.; Hod, M.; Ben-Rafael, Z.; Weinberger, I.; Brosens, J.:

    Regulation of Platelet Aggregation and Adenosine Triphosphate Release In Vitro by 17β-Estradiol and Medroxyprogesterone Acetate in Postmenopausal Women

  • 701
    Ikari, Yuji; Yee, Karen O.; Schwartz, Stephen M.:

    Role of α5β1 and αvβ3 Integrins on Smooth Muscle Cell Spreading and Migration in Fibrin Gels

  • 706
    Dichtl, Wolfgang; Ares, Mikko P. S.; Stollenwerk, Maria; Giachelli, Cecilia M.; Scatena, Marta; Hamsten, Anders; Eriksson, Per; Nilsson, Jan:

    In Vivo Stimulation of Vascular Plasminogen Activator Inhibitor-1 Production by very Low-Density Lipoprotein Involves Transcription Factor Binding to a VLDL-Responsive Element

  • 712
    Ishii, Hidemi; Takada, Kimihiko; Higuchi, Toshiyuki; Sugiyama, Junichi:

    Verotoxin-1 Induces Tissue Factor Expression in Human Umbilical Vein Endothelial Cells through Activation of NF-κB/Rel and AP-1

    • Letters to the Editor

  • 722
    Arnaud, Emmanuel; Poirier, Odette; MONICA Members Group; Aiach, Martine; Cambien, Françcois:

    The -506I/D Polymorphism of the Thrombin Receptor (PAR-1) Gene Is not Related to Myocardial Infarction in the ECTIM Study

  • 723
    Mikovic, Danijela; Rakicevic, Ljiljana; Kovac, Mirjana; Radojkovic, Dragica:

    Prevalence of Factor V Leiden Mutation in Yugoslav Thrombophilic Patients and Its Relationship to the Laboratory Diagnosis of APC Resistance

  • 724
    Hessner, Martin J.; Luhm, Robert A.:

    The C536T Transition in the Tissue Factor Pathway Inhibitor (TFPI) Gene Does not Contribute to Risk of Venous Thrombosis among Carriers of Factor V Leiden

  • 726
    Margaglione, Maurizio; Di Castelnuovo, Augusto; Totaro, Angela; Iacoviello, Licia; Di Minno, Giovanni:

    Risk of Myocardial Infarction in Carriers of Mutations in the Hemochromatosis-associated Gene

  • 727
    Veyradier, Agnès; Fressinaud, Edith; Boyer-Neumann, Catherine; Trossaert, Marc; Meyer, Dominique:

    von Willebrand Factor Ristocetin Cofactor Activity Correlates with Platelet Function in a High Shear Stress System

  • 729
    Castaman, Giancarlo; Eikenboom, Jeroen C. J.; Lattuada, Antonella; Rodeghiero, Francesco:

    Grossly Abnormal Proteolysis of von Willebrand Factor (VWF) in a Patient Heterozygous for a Gene Deletion and Mutation in the Dimerization Area of VWF

  • 730
    Lowe, Gordon; Rumley, Ann; Woodward, Mark; Vessey, Martin:

    C-reactive Protein, Idiopathic Venous Thromboembolism and Hormone Replacement Therapy

  • 731
    Osmanovic, Nada; Romijn, Fred P. H. T. M.; Joop, Karin; Sturk, Augueste; Nieuwland, Rienk:

    Soluble Selectins in Sepsis: Microparticle-associated, but only to a Minor Degree

  • 733
    Rommel, Franz; Toepfer, Marcell; Eberle, Josef; Schiffl, Helmut; Spannagl, Michael; Schramm, Wolfgang:

    Reactivation of Chronic Hepatitis C Virus Infection by Immunoadsorption in Factor VIII Inhibitor Haemophilia

  • 734
    De Curtis, Amalia; D’Adamo, Maria Cristina; Amore, Concetta; Donati, Maria Benedetta; Iacoviello, Licia:

    Effects of Dyslipidemia on t-PA Release in Rats

  • 735
    Moore, J.; Aboud, M.; Ma, D.:

    Adult Transient Lupus Anticoagulant Patients Maintain an Acquired Activated Protein C Resistance Profile

  • 736
    Kawasaki, T.; Fujimura, H.; Kakinoki, E.; Uemichi, A.; Miyata, T.:

    Is there a Role for Genetic Polymorphism of C677T Methylenetetrahydrofolate Reductase (MTHFR) in Buerger’s Disease?

  • 737
    Kelly, Peter J.; Furie, Karen L.:

    Hyperhomocyst(e)inemia, MTHFR 677C→T Polymorphism and Folate Status in Acute Coronary Disease

  • 738
    Planes, A.:

    Prevention of Deep Vein Thrombosis after Hip Replacement - Reply