Biochemical and Functional Properties of Factor XI and Prekallikrein von Mannhalter, Christine H.

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Mean platelet volume is an independent risk factor for myocardial infarction but not for coronary artery disease von Endler, Georg, Klimesch, Alexandra, Sunder‐Plassmann, Heike, Schillinger, Martin, Exner, Markus, Mannhalter, Christine, Jordanova, Nelli, Christ, Günter, Thalhammer, Renate, Huber, Kurt, Sunder‐Plassmann, Raute

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Temporary increase in the risk for recurrence during pregnancy in women with a history of venous thromboembolism von Pabinger, Ingrid, Grafenhofer, Helga, Kyrle, Paul A., Quehenberger, Peter, Mannhalter, Christine, Lechner, Klaus, Kaider, Alexandra

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EVI1 and MDS1/EVI1 Expression During Primary Human Hematopoietic Progenitor Cell Differentiation into Various Myeloid Lineages von STEINLEITNER, Katarina, RAMPETSREITER, Paulina, KÖFFEL, Rene, RAMANATHAN, Gajalakshmi, MANNHALTER, Christine, STROBL, Herbert, WIESER, Rotraud

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The effect of p22-PHOX (CYBA) polymorphisms on premature coronary artery disease (≤ 40 years of age) von Goliasch, Georg, Wiesbauer, Franz, Grafl, Andreas, Ponweiser, Elisabeth, Blessberger, Hermann, Tentzeris, Ioannis, Wojta, Johann, Schillinger, Martin, Huber, Kurt, Maurer, Gerald, Mannhalter, Christine, Sunder-Plaßmann, Raute

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Risk of recurrence after a first venous thromboembolic event in young women von Laczkovics, Clarissa, Grafenhofer, Helga, Kaider, Alexandra, Quehenberger, Peter, Simanek, Ralph, Mannhalter, Christine, Lechner, Klaus, Pabinger, Ingrid

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A Meta-Analysis of Candidate Gene Polymorphisms and Ischemic Stroke in 6 Study Populations : Association of Lymphotoxin-Alpha in Nonhypertensive Patients von XINGYU WANG, SUZANNE CHENG, KESSLER, Christof, LUEDEMANN, Jan, LINDPAINTNER, Klaus, LISHENG LIU, RIDKER, Paul M, ZEE, Robert Y. L, COOK, Nancy R, BROPHY, Victoria H, ERLICH, Henry A, MANNHALTER, Christine, BERGER, Klaus, LALOUSCHEK, Wolfgang, BROWNER, Warren S, YU SHI, BERND RINGELSTEIN, E

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A Single Genetic Origin for the Common Prothrombotic G20210A Polymorphism in the Prothrombin Gene von Zivelin, Ariella, Rosenberg, Nurit, Faier, Shlomit, Kornbrot, Nurit, Peretz, Hava, Mannhalter, Christine, Horellou, Marie Helene, Seligsohn, Uri

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Abstract TMP50: A Polymorphism in HDAC9 was Associated with Large Vessel Stroke in the Vienna and German Stroke Studies von Luke, May M, Tong, Carmen H, Catanese, Joseph J, Devlin, James J, Mannhalter, Christine, Berger, Klaus

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Spectrum of causative mutations in patients with haemophilia A in Austria von Reitter, Sylvia, Sturn, Rümuth, Horvath, Birgit, Freitag, Renate, Male, Christoph, Muntean, Wolfgang, Streif, Werner, Pabinger, Ingrid, Mannhalter, Christine

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Protein C promoter polymorphisms associate with sepsis in children with systemic meningococcemia von BINDER, Alexander, ENDLER, Georg, RIEGER, Sandra, GEISHOFER, Gotho, RESCH, Bernhard, MANNHALTER, Christine, ZENZ, Werner

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Donor heme oxygenase-1 genotype is associated with renal allograft function von EXNER, Markus, BOHMIG, Georg A, SCHILLINGER, Martin, REGELE, Heinz, WATSCHINGER, Bruno, HÖRL, Walter H, RAITH, Marianne, MANNHALTER, Christine, WAGNER, Oswald F

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Most CD56 + Intestinal Lymphomas Are CD8 +CD5 − T-Cell Lymphomas of Monomorphic Small to Medium Size Histology von Chott, Andreas, Haedicke, Wolfgang, Mosberger, Isabella, Födinger, Manuela, Winkler, Karin, Mannhalter, Christine, Müller-Hermelink, Hans-Konrad

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Heme oxygenase-1 gene promoter polymorphism is associated with abdominal aortic aneurysm von Schillinger, Martin, Exner, Markus, Mlekusch, Wolfgang, Domanovits, Hans, Huber, Kurt, Mannhalter, Christine, Wagner, Oswald, Minar, Erich

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Fractalkine receptor polymorphisms V249I and T280M as genetic risk factors for restenosis von Niessner, Alexander, Marculescu, Rodrig, Kvakan, Heda, Haschemi, Arvand, Endler, Georg, Weyand, Cornelia M., Maurer, Gerald, Mannhalter, Christine, Wojta, Johann, Wagner, Oswald, Huber, Kurt

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Factor V Leiden mutation carriership and venous thromboembolism in polycythemia vera and essential thrombocythemia von Ruggeri, Marco, Gisslinger, Heinz, Tosetto, Alberto, Rintelen, Claudia, Mannhalter, Christine, Pabinger, Ingrid, Heis, Navide, Castaman, Giancarlo, Missiaglia, Edoardo, Lechner, Klaus, Rodeghiero, Francesco

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A Single Genetic Origin for the Common Prothrombotic G20210A Polymorphism in the Prothrombin Gene von Zivelin, Ariella, Rosenberg, Nurit, Faier, Shlomit, Kornbrot, Nurit, Peretz, Hava, Mannhalter, Christine, Horellou, Marie Helene, Seligsohn, Uri

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Preeclampsia and Fetal Loss in Women With a History of Venous Thromboembolism von Pabinger, Ingrid, Grafenhofer, Helga, Kaider, Alexandra, Ilic, Adriana, Eichinger, Sabine, Quehenberger, Peter, Husslein, Peter, Mannhalter, Christine, Lechner, Klaus

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ABO mismatch increases transplant-related morbidity and mortality in patients given nonmyeloablative allogeneic HPC transplantation von Worel, Nina, Kalhs, Peter, Keil, Felix, Prinz, Erika, Moser, Karin, Schulenburg, Axel, Mitterbauer, Margit, Mannhalter, Christine, Mayr, Wolfgang R., Schwarzinger, Ilse, Höcker, Paul, Lechner, Klaus, Greinix, Hildegard T.

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Donor leukocyte infusion for leukemic relapse after allogeneic marrow transplantation : Lack of residual donor hematopoiesis predicts aplasia von KEIL, F, HAAS, O. A, FRITSCH, G, KALHS, P, LECHNER, K, MANNHALTER, C, REITER, E, NIEDERWIESER, D, HOECKER, P, GREINIX, H. T

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