DOI: 10.1055/s-00035024

Thrombosis and Haemostasis

Issue 09 · Volume 98 · 2007 DOI: 10.1055/s-008-36077

Theme Issue Editorial

  • 483
    Herwald, Heiko:

    Haemostasis, vascular biology, and infectious agents

  • 485
    Frutos, Pablo García de:

    Mechanisms of thrombophilia

    • Theme Issue Article

  • 488
    Nitsche-Schmitz, Patric D.; Rohde, Manfred; Chhatwal, Gursharan S.:

    Invasion mechanisms of Gram-positive pathogenic cocci

  • 497
    Frick, Inga-Maria; Björck, Lars; Herwald, Heiko:

    The dual role of the contact system in bacterial infectious disease

  • 503
    Rivera, Jose; Vannakambadi, Ganesh; Höök, Magnus; Speziale, Pietro:

    Fibrinogen-binding proteins of Gram-positive bacteria

  • 512
    Bergmann, Simone; Hammerschmidt, Sven:

    Fibrinolysis and host response in bacterial infections

  • 521
    Aepfelbacher, Martin; Trasak, Claudia; Ruckdeschel, Klaus:

    Effector functions of pathogenic Yersinia species

  • 530
    Segers, Kenneth; Dahlbäck, Björn; Nicolaes, Gerry A. F.:

    Coagulation factor V and thrombophilia: Background and mechanisms

  • 543
    Frutos, Pablo García de; Fuentes-Prior, Pablo; Hurtado, Begoña; Sala, Núria:

    Molecular basis of protein S deficiency

  • 557
    Hernández-Espinosa, David; Ordóñez, Adriana; Vicente, Vicente; Corral, Javier:

    Factors with conformational effects on haemostatic serpins: Implications in thrombosis

  • 564
    Medina, Pilar; Navarro, Silvia; Estellés, Amparo; España, Francisco:

    Polymorphisms in the endothelial protein C receptor gene and thrombophilia

  • 570
    Oldenburg, Johannes; Bevans, Carville G.; Fregin, Andreas; Geisen, Christof; Müller-Reible, Clemens; Watzka, Matthias:

    Current pharmacogenetic developments in oral anticoagulation therapy: The influence of variant VKORC1 and CYP2C9 alleles

    • Review Article

  • 579
    Cornet, Alexander D.; Smit, Ellen G. M.; Beishuizen, Albertus; Groeneveld, A. B. Johan:

    The role of heparin and allied compounds in the treatment of sepsis

    • Blood Coagulation, Fibrinolysis and Cellular Haemostasis

  • 587
    Hasstedt, Sandra J.; Scott, Bruce T.; Rosendaal, Frits R.; Callas, Peter W.; Vossen, Carla Y.; Long, George L.; Bovill, Edwin G.:

    Exclusion of the α2 subunit of platelet-activating factor acetylhydrolase 1b (PAFAH1B2) as a prothrombotic gene in a protein C-deficient kindred and population-based case-control sample

  • 593
    Hommais, Antoine; Rayes, Julie; Houllier, Anne; Obert, Bernadette; Legendre, Paulette; Veyradier, Agnes; Girma, Jean-Pierre; Ribba, Anne-Sophie:

    Molecular characterization of four ADAMTS13 mutations responsible for congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome)

  • 600
    Devreese, Katrien; Wijns, Walter; Combes, Isabelle; Vankerckhoven, Soetkin; Hoylaerts, Marc F.:

    Thrombin generation in plasma of healthy adults and children: Chromogenic versus fluorogenic thrombogram analysis

  • 614
    Desbuards, Nicolas; Rochefort, Gaël Y.; Schlecht, Deborah; Machet, Marie-Christine; Halimi, Jean-Michel; Eder, Véronique; Hyvelin, Jean-Marc; Antier, Daniel:

    Heme oxygenase-1 inducer hemin prevents vascular thrombosis

  • 621
    Vayá, Amparo; Falcó, Cristina; Simó, María; Ferrando, Fernando; Mira, Yolanda; Todolí, José; España, Francisco; Corella, Dolores:

    Influence of lipids and obesity on haemorheological parameters in patients with deep vein thrombosis

    • Endothelium and Vascular Development

  • 627
    Iakhiaev, Alexei V.; Rezaie, Alireza R.; Idell, Steven:

    Thrombomodulin-mediated catabolism of protein C by pleural mesothelial and vascular endothelial cells

  • 635
    Iorio, Alfonso; Federici, Marco Orsini; Mourvaki, Evangelia; Ferolla, Piero; Piroddi, Marta; Stabile, Anna; Timi, Alessandra; Celleno, Roberta; Benedetti, Massimo Massi:

    Impaired endothelial antithrombotic activity following short-term interruption of continuous subcutaneous insulin infusion in type1 diabetic patients

    • Cardiovascular Biology and Cell Signalling

  • 642
    Nisio, Marcello Di; Febbo, Concetta Di; Moretta, Valeria; Guglielmi, Maria Domenica; Stuppia, Liborio; Cuccurullo, Franco; Porreca, Ettore:

    Effects of toll-like receptor-4 gene polymorphisms on soluble P-selectin and von Willebrand factor levels in hypercholesterolemic patients

  • 648
    Castelnuovo, Augusto Di; Quacquaruccio, Gianni; Jozef, Arnout; Cappuccio, Francesco Paolo; Lorgeril, Michel de; Dirckx, Carla; Donati, Maria Benedetta; Krogh, Vittorio; Siani, Alfonso; van Dongen, Marten C. J. M.; Zito, Francesco; Gaetano, Giovanni de; Iacoviello, Licia; European Collaborative Group of the Project; on behalf of:

    Cardiovascular risk factors and global risk of fatal cardiovascular disease are positively correlated between partners of 802 married couples from different European countries

    • Cellular Proteolysis and Oncology

  • 656
    Seddighzadeh, Ali; Shetty, Ranjith; Goldhaber, Samuel Z.:

    Venous thromboembolism in patients with active cancer

    • Animal Models

  • 662
    Vilahur, Gemma; Casaní, Laura; Badimon, Lina:

    A thromboxane A2/prostaglandin H2 receptor antagonist (S18886) shows high antithrombotic efficacy in an experimental model of stent-induced thrombosis

  • 670
    Spek, Arnold C.; ten Kate, Fiebo J. W.; te Velde, Anje A.:

    Factor V Leiden and the etiology of inflammatory bowel disease

    • New Technologies, Diagnostic Tools and Drugs

  • 674
    Dommke, Christoph; Haase, Karl K.; Süselbeck, Tim; Streitner, Ines; Haghi, Dariush; Metz, Jürgen; Borggrefe, Martin; Herdeg, Christian:

    Local paclitaxel delivery after coronary stenting in an experimental animal model

    • Case Report

  • 681
    Plumé, Gema; Vayá, Amparo; Ferrando, Fernando; Mira, Yolanda; Orbis, Francisco:

    JAK2V617F mutation as a marker of a latent myeloproliferative disorder in a patient with Budd-Chiari syndrome and factor V Leiden mutation

    • Letters to the Editor

  • 683
    Cai, Xiao-Hong; Wang, Xue-Feng; Ding, Qiu-Lan; Fu, Qi-Hua; Wang, Hong-Li:

    FactorV C1149G and 5609–10INSCGTGGTT causing factor V deficiency: Molecular characterization by in-vitro expression

  • 685
    Milojkovic, Dragana; Patel, Raj; Ford, Elizabeth; Arya, Roopen; Mufti, Ghulam:

    Acquired factor V inhibitor after haematopoietic stem cell transplantation

  • 687
    Zhidong, Wang; Xiaojun, Huang:

    Severe factor VII deficiency caused by a novel point mutation (Arg353Pro) combined with a rare Cys22Arg mutation

  • 689
    Hanss, Michel; Chevreaud, Caroline; French, Patrick; Négrier, Claude; Mazancourt, Philippe de:

    Clinical and biological features of 3 cases of hypofibrinogenemia associated with three different mutations(γAla341Thr, Bβ Tyr326Cys and Aα Asp496Asn)

  • 691
    Gatt, Alex; van Veen, Joost J.; Cooper, Peter; Kitchen, Steve; Makris, Michael:

    Protein C deficiency screening using a thrombin generation assay – An upgrade

  • 693
    André, Elisabeth; Hacquard, Marie; Alnot, Yveline; Maistre, Emmanuel de; Lecompte, Thomas:

    Activated protein C resistance test using factor VIII-deficient plasma: A new approach to the venous thrombotic risk?

  • 695
    Rossi, Elena; Chiusolo, Patrizia; Za, Tommaso; Marietti, Sara; Ciminello, Angela; Leone, Giuseppe; Stefano, Valerio De:

    Report of a novel kindred with antithrombin heparin-binding site variant (47 Arg to His): Demand for an automated progressive antithrombin assay to detect molecular variants with low thrombotic risk

  • 697
    Stankiewicz, Adrian; Gromotowicz, Anna; Szemraj, Janusz; Wojewódzka-Źelezniakowicz, Marzena; Skrzypkowski, Przemyslaw; Chabielska, Ewa:

    Acute aldosterone infusion enhances thrombosis development in normotensive rats

  • 699
    Poulou, Loukia S.; Vakrinos, George; Pomoni, Anastasia; Michalakis, Kostis; Karianakis, George; Voulgarelis, Michael; Ziakas, Panayiotis D.:

    Stroke in paroxysmal nocturnal haemoglobinuria: Patterns of disease and outcome

  • 702
    Randi, Maria L.; Lombardi, Anna Maria; Scapin, Margherita; Tezza, Fabiana; Scandellari, Raffaella; Ruzzon, Elisabetta; Duner, Elena; Fabris, Fabrizio:

    Haemostatic proteins gene polymorphisms in patients with unusual vein thrombosis and Ph-myeloproliferative disorders