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Founder effect is responsible for the p.Leu131Phe heparin‐binding‐site antithrombin mutation common in Hungary: phenotype analysis in a large cohort

Journal of thrombosis and haemostasis, 2016-04, Vol.14 (4), p.704-715

2016

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The involvement of blood coagulation factor XIII in fibrinolysis and thrombosis

Cardiovascular & hematological agents in medicinal chemistry, 2008-07, Vol.6 (3), p.190

2008

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Alloantibody developed in a factor XIII A subunit deficient patient during substitution therapy; characterization of the antibody

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-03, Vol.22 (2), p.268-275

2016

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Evidence for the founder effect of a novel ACVRL1 splice-site mutation in Hungarian hereditary hemorrhagic telangiectasia families

Clinical genetics, 2016-11, Vol.90 (5), p.466-467

2016

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First Report of Oidium longipes as the Causal Agent of Petunia Powdery Mildew in the United Kingdom

Plant disease, 2011-03, Vol.95 (3), p.361-361

2011

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The use of recombinant factor XIII in a major bleeding episode of a patient with congenital factor XIII deficiency - the first experience

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-01, Vol.21 (1), p.e118-e121

2015

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C0290: Diagnostic Considerations Based on the Experience of Genetic Analysis in Protein S Deficiency in the Hungarian Population with High Frequency of FV Leiden Mutation

Thrombosis research, 2014-05, Vol.133, p.S81-S81

2014

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C0384: High Prevalence of Antithrombin Budapest 3 Mutation in Hungary, Investigation of Founder Effect

Thrombosis research, 2014-05, Vol.133, p.S11-S12

2014

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Elevated factor XIII level and the risk of myocardial infarction in women

Haematologica (Roma), 2007-02, Vol.92 (2), p.287-288

2007

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Factor XIII deficiency: complete phenotypic characterization of two cases with novel causative mutations

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-01, Vol.20 (1), p.114-120

2014

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C0337: Molecular Characterization of Novel Protein C Mutations (p.Asp77Gly, p.Ala163Val and p.Ala163Glu) Causing Protein C Deficiency

Thrombosis research, 2014-05, Vol.133, p.S11-S11

2014

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Metabolic risk factors in patients with renal stones in KwaZulu Natal: an inter‐racial study (Asian and Whites)

BJU international, 2004-01, Vol.93 (1), p.120-123

2004

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PB1210 Incorporation of a2-Plasmin Inhibitor into Plasma Clots of Patients with Venous Thrombosis

Research and practice in thrombosis and haemostasis, 2023-10, Vol.7, p.101033, Article 101033

2023

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Factor XDebrecen: Gly204Arg mutation in factor X causes the synthesis of a non-secretable protein and severe factor X deficiency

Haematologica (Roma), 2008-02, Vol.93 (2), p.299-302

2008

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O2 Interaction between homocysteine and lipoprotein(a) increases the risk of coronary sclerosis/myocardial infarction in women

Thrombosis research, 2009, Vol.123, p.S131-S131

2009

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HAEMOSTASIS CHANGES AND ENDOTHELIUM ACTIVATION DURING PERCUTANEOUS TRANSCATHETER ISOLATION OF THE PULMONARY VEINS IN PATIENTS WITH ATRIAL FIBRILLATION

Canadian journal of cardiology, 2015, Vol.31 (10), p.S255-S255

2015

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PB1381 Value of Next-Generation Sequencing in the Diagnosis of Platelet Function Disorders

Research and practice in thrombosis and haemostasis, 2023-10, Vol.7, p.101526, Article 101526

2023

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The Tomato fer Gene Encoding a bHLH Protein Controls Iron-Uptake Responses in Roots

Proceedings of the National Academy of Sciences - PNAS, 2002-10, Vol.99 (21), p.13938-13943

2002

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Clinical Investigation of Hereditary and Acquired Thrombophilic Factors in Patients with Venous and Arterial Thromboembolism

International journal of general medicine, 2023-11, Vol.16, p.5425-5437

2023

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Differential Regulation of nramp and irt Metal Transporter Genes in Wild Type and Iron Uptake Mutants of Tomato

The Journal of biological chemistry, 2003-07, Vol.278 (27), p.24697-24704

2003

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10 Elevated factor XIII level represents an increased risk of myocardial infarction in women

Thrombosis research, 2007, Vol.119, p.S99-S100

2007

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P049 Could heparin-induced thrombocytopenia and thrombosis be a rare manifestation of antiphospholipid antibody syndrome?

Blood reviews, 2007, Vol.21, p.S101-S102

2007

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OC 17.3 Prothrombotic Polymorphisms FV Leiden and Prothrombin G20210A in 699 Unrelated Patients with Congenital Antithrombin Deficiency: More than a Prognostic Value

Research and practice in thrombosis and haemostasis, 2023-10, Vol.7, p.100627, Article 100627

2023

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HAEMOSTASIS CHANGES AND ENDOTHELIUM ACTIVATION DURING PERCUTANEOUS TRANSCATHETER ISOLATION OF THE PULMONARY VEINS IN PATIENTS WITH ATRIAL FIBRILLATION

Canadian journal of cardiology, 2015-10, Vol.31 (10), p.S255-S255

2015

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PS1577 PLATELET COUNT AND MEAN PLATELET VOLUME IN ACUTE STROKE: A SYSTEMATIC REVIEW AND META‐ANALYSIS

HemaSphere, 2019-06, Vol.3 (S1), p.726-727

2019

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Founder effect is responsible for the p.Leu131Phe heparin‐binding‐site antithrombin mutation common in Hungary: phenotype analysis in a large cohort

The involvement of blood coagulation factor XIII in fibrinolysis and thrombosis

Alloantibody developed in a factor XIII A subunit deficient patient during substitution therapy; characterization of the antibody

Evidence for the founder effect of a novel ACVRL1 splice-site mutation in Hungarian hereditary hemorrhagic telangiectasia families

First Report of Oidium longipes as the Causal Agent of Petunia Powdery Mildew in the United Kingdom

The use of recombinant factor XIII in a major bleeding episode of a patient with congenital factor XIII deficiency - the first experience

C0290: Diagnostic Considerations Based on the Experience of Genetic Analysis in Protein S Deficiency in the Hungarian Population with High Frequency of FV Leiden Mutation

C0384: High Prevalence of Antithrombin Budapest 3 Mutation in Hungary, Investigation of Founder Effect

Elevated factor XIII level and the risk of myocardial infarction in women

Factor XIII deficiency: complete phenotypic characterization of two cases with novel causative mutations

C0337: Molecular Characterization of Novel Protein C Mutations (p.Asp77Gly, p.Ala163Val and p.Ala163Glu) Causing Protein C Deficiency

Metabolic risk factors in patients with renal stones in KwaZulu Natal: an inter‐racial study (Asian and Whites)

PB1210 Incorporation of a2-Plasmin Inhibitor into Plasma Clots of Patients with Venous Thrombosis

Factor XDebrecen: Gly204Arg mutation in factor X causes the synthesis of a non-secretable protein and severe factor X deficiency

O2 Interaction between homocysteine and lipoprotein(a) increases the risk of coronary sclerosis/myocardial infarction in women

HAEMOSTASIS CHANGES AND ENDOTHELIUM ACTIVATION DURING PERCUTANEOUS TRANSCATHETER ISOLATION OF THE PULMONARY VEINS IN PATIENTS WITH ATRIAL FIBRILLATION

PB1381 Value of Next-Generation Sequencing in the Diagnosis of Platelet Function Disorders

The Tomato fer Gene Encoding a bHLH Protein Controls Iron-Uptake Responses in Roots

Clinical Investigation of Hereditary and Acquired Thrombophilic Factors in Patients with Venous and Arterial Thromboembolism

Differential Regulation of nramp and irt Metal Transporter Genes in Wild Type and Iron Uptake Mutants of Tomato

10 Elevated factor XIII level represents an increased risk of myocardial infarction in women

P049 Could heparin-induced thrombocytopenia and thrombosis be a rare manifestation of antiphospholipid antibody syndrome?

OC 17.3 Prothrombotic Polymorphisms FV Leiden and Prothrombin G20210A in 699 Unrelated Patients with Congenital Antithrombin Deficiency: More than a Prognostic Value

HAEMOSTASIS CHANGES AND ENDOTHELIUM ACTIVATION DURING PERCUTANEOUS TRANSCATHETER ISOLATION OF THE PULMONARY VEINS IN PATIENTS WITH ATRIAL FIBRILLATION

PS1577 PLATELET COUNT AND MEAN PLATELET VOLUME IN ACUTE STROKE: A SYSTEMATIC REVIEW AND META‐ANALYSIS

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