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4‐Thio‐deoxyuridylate‐modified thrombin aptamer and its inhibitory effect on fibrin clot formation, platelet aggregation and thrombus growth on subendothelial matrix

Journal of thrombosis and haemostasis, 2008-10, Vol.6 (10), p.1764-1771

2008

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Evaluation of Mannose-Binding Lectin is a Useful Approach to Predict the Risk of Infectious Complications Following Autologous Hematopoietic Stem Cell Transplantation

Transplantation proceedings, 2016-12, Vol.48 (10), p.3397-3405

2016

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P037 Haptoglobin polymorphism in patients with chronic lymphocytic leukemia

Blood reviews, 2007, Vol.21, p.S97-S98

2007

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AB0632 Assessment of vegf and other cytokines in the tear of patients with systemic sclerosis

Annals of the rheumatic diseases, 2017-06, Vol.76 (Suppl 2), p.1273

2017

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Haptoglobin (2-2) Polymorphism together with elevated homocystein level enhance the risk for subclinical atherosclerosis in type 2 diabetic men

Atherosclerosis, 2015-07, Vol.241 (1), p.e179-e180

2015

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The effect of haptoglobin polymorphism and rosiglitazone treatment on the carotid artery intima-media thickness in type 2 diabetic patients – A 7-year follow-up

Atherosclerosis, 2015-07, Vol.241 (1), p.e179-e179

2015

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Follow up of thrombin-generation after prostate cancer surgery

Thrombosis research, 2012-04, Vol.129, p.S190-S190

2012

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Increased platelet activation and decreased fibrinolysis in the pathogenesis of aseptic necrosis of the femoral head

Platelets (Edinburgh), 1998, Vol.9 (3-4), p.233-235

1998

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Identification of a VWF peptide antagonist that blocks platelet adhesion under high shear conditions by selectively inhibiting the VWF‐collagen interaction

Journal of thrombosis and haemostasis, 2009-10, Vol.7 (10), p.1680-1687

2009

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262 THE ALTERATIONS OF VON WILLEBRAND FACTOR AND ITS CLEAVING PROTEASE, ADAMTS-13 SHOW AN OPPOSITE CHANGE OF DIRECTION IN PATIENTS WITH LIVER CIRRHOSIS

Journal of hepatology, 2008, Vol.48, p.S106-S106

2008

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The most severe forms of Perthes' disease associated with the homozygous Factor V Leiden mutation

Journal of bone and joint surgery. British volume, 2004-04, Vol.86 (3), p.426-429

2004

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687 THE HAPTOGLOBIN 1–1 GENOTYPE HAS A POSSIBLE PROTECTIVE EFFECT AGAINST PRIMARY SCLEROSING CHOLANGITIS

Journal of hepatology, 2009, Vol.50, p.S252-S252

2009

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183 MANNOSE-BINDING LECTIN DEFICIENCY CONFERS RISK FOR INFECTIONS IN A LARGE HUNGARIAN COHORT OF PATIENTS WITH LIVER CIRRHOSIS

Journal of hepatology, 2010, Vol.52, p.S79-S79

2010

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Altered primary haemostasis in Conn's syndrome

Thrombosis research, 1992-09, Vol.67 (5), p.625-628

1992

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Factor XIII mediates adhesion of platelets to endothelial cells through αvβ3 and glycoprotein IIb/IIIa integrins

Thrombosis research, 2002-02, Vol.105 (4), p.317-323

2002

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Treatment of the severe bleeding episode in type III von Willebrand's disease by simultaneous administration of cryoprecipitate and platelet concentrate

Blood coagulation & fibrinolysis, 1991-12, Vol.2 (6), p.775

1991

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Cyclosporin treatment of a woman with acquired haemophilia due to factor VIII:C inhibitor

Postgraduate medical journal, 1989-06, Vol.65 (764), p.400-402

1989

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Selection of phages that inhibit vWF interaction with collagen under both static and flow conditions

Thrombosis and haemostasis, 2001-08, Vol.86 (2), p.630-635

2001

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A monoclonal antibody directed against human von Willebrand factor induces type 2B‐like alterations

Journal of thrombosis and haemostasis, 2004-09, Vol.2 (9), p.1622-1628

2004

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Follow-up of thrombin generation after prostate cancer surgery: global test for increased hypercoagulability

PloS one, 2012-12, Vol.7 (12), p.e51299-e51299

2012

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The subendothelium of the HMEC-1 cell line supports thrombus formation in the absence of von Willebrand factor and collagen types I, III and VI

Thrombosis and haemostasis, 2001-03, Vol.85 (3), p.552-559

2001

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Shear-dependent morphology of von Willebrand factor bound to immobilized collagen

Blood, 2002-03, Vol.99 (6), p.2070-2076

2002

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Thrombotic changes in haemostasis following intravenous streptokinase treatment for acute myocardial infarction

Thrombosis and haemostasis, 1990, Vol.63 (1), p.146-147

1990

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Alterations of primary haemostasis in mixed connective tissue disease (MCTD)

Thrombosis research, 1991-08, Vol.63 (3), p.281-286

1991

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Endothelium releases more von Willebrand factor and tissue-type plasminogen activator upon venous occlusion in patients with liver cirrhosis than in normals

Haemostasis, 1993, Vol.23 (1), p.58-64

1993

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4‐Thio‐deoxyuridylate‐modified thrombin aptamer and its inhibitory effect on fibrin clot formation, platelet aggregation and thrombus growth on subendothelial matrix

Evaluation of Mannose-Binding Lectin is a Useful Approach to Predict the Risk of Infectious Complications Following Autologous Hematopoietic Stem Cell Transplantation

P037 Haptoglobin polymorphism in patients with chronic lymphocytic leukemia

AB0632 Assessment of vegf and other cytokines in the tear of patients with systemic sclerosis

Haptoglobin (2-2) Polymorphism together with elevated homocystein level enhance the risk for subclinical atherosclerosis in type 2 diabetic men

The effect of haptoglobin polymorphism and rosiglitazone treatment on the carotid artery intima-media thickness in type 2 diabetic patients – A 7-year follow-up

Follow up of thrombin-generation after prostate cancer surgery

Increased platelet activation and decreased fibrinolysis in the pathogenesis of aseptic necrosis of the femoral head

Identification of a VWF peptide antagonist that blocks platelet adhesion under high shear conditions by selectively inhibiting the VWF‐collagen interaction

262 THE ALTERATIONS OF VON WILLEBRAND FACTOR AND ITS CLEAVING PROTEASE, ADAMTS-13 SHOW AN OPPOSITE CHANGE OF DIRECTION IN PATIENTS WITH LIVER CIRRHOSIS

The most severe forms of Perthes' disease associated with the homozygous Factor V Leiden mutation

687 THE HAPTOGLOBIN 1–1 GENOTYPE HAS A POSSIBLE PROTECTIVE EFFECT AGAINST PRIMARY SCLEROSING CHOLANGITIS

183 MANNOSE-BINDING LECTIN DEFICIENCY CONFERS RISK FOR INFECTIONS IN A LARGE HUNGARIAN COHORT OF PATIENTS WITH LIVER CIRRHOSIS

Altered primary haemostasis in Conn's syndrome

Factor XIII mediates adhesion of platelets to endothelial cells through αvβ3 and glycoprotein IIb/IIIa integrins

Treatment of the severe bleeding episode in type III von Willebrand's disease by simultaneous administration of cryoprecipitate and platelet concentrate

Cyclosporin treatment of a woman with acquired haemophilia due to factor VIII:C inhibitor

Selection of phages that inhibit vWF interaction with collagen under both static and flow conditions

A monoclonal antibody directed against human von Willebrand factor induces type 2B‐like alterations

Follow-up of thrombin generation after prostate cancer surgery: global test for increased hypercoagulability

The subendothelium of the HMEC-1 cell line supports thrombus formation in the absence of von Willebrand factor and collagen types I, III and VI

Shear-dependent morphology of von Willebrand factor bound to immobilized collagen

Thrombotic changes in haemostasis following intravenous streptokinase treatment for acute myocardial infarction

Alterations of primary haemostasis in mixed connective tissue disease (MCTD)

Endothelium releases more von Willebrand factor and tissue-type plasminogen activator upon venous occlusion in patients with liver cirrhosis than in normals

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