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Factor XIII: novel structural and functional aspects

Journal of thrombosis and haemostasis, 2011-01, Vol.9 (1), p.9-20

2011

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Auto‐ and alloantibodies against factor XIII: laboratory diagnosis and clinical consequences

Journal of thrombosis and haemostasis, 2018-05, Vol.16 (5), p.822-832

2018

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Diagnosis and classification of factor XIII deficiencies

Journal of thrombosis and haemostasis, 2011-07, Vol.9 (7), p.1404-1406

2011

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Mechanism of the irreversible inhibition of human cyclooxygenase-1 by aspirin as predicted by QM/MM calculations

Journal of molecular graphics & modelling, 2013-03, Vol.40, p.99-109

2013

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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.190-205

2008

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Minimal factor XIII activity level to prevent major spontaneous bleeds

Journal of thrombosis and haemostasis, 2017-09, Vol.15 (9), p.1728-1736

2017

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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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Neutralizing autoantibody against factor XIII A subunit resulted in severe bleeding diathesis with a fatal outcome – characterization of the antibody

Journal of thrombosis and haemostasis, 2016-08, Vol.14 (8), p.1517-1520

2016

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Factor XIII: recommended terms and abbreviations

Journal of thrombosis and haemostasis, 2007-01, Vol.5 (1), p.181-183

2007

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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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Prophylactic and perioperative replacement therapy for acquired factor XIII deficiency: a rebuttal

Journal of thrombosis and haemostasis, 2004-11, Vol.2 (11), p.2075-2077

2004

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Severe bleeding diatheses in an elderly patient with combined type autoantibody against factor XIII A subunit; novel approach to the diagnosis and classification of anti‐factor XIII antibodies

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-07, Vol.23 (4), p.590-597

2017

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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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Plasma clot properties in patients with a mild-to-moderate bleeding tendency of unknown cause

Annals of hematology, 2015-08, Vol.94 (8), p.1301-1310

2015

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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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Molecular mechanism of the interaction between activated factor XIII and its glutamine donor peptide substrate

Journal of thrombosis and haemostasis, 2009-04, Vol.7 (4), p.627-633

2009

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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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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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A Modified, Optimized Kinetic Photometric Assay for the Determination of Blood Coagulation Factor XIII Activity in Plasma

Clinical chemistry (Baltimore, Md.), 2000-12, Vol.46 (12), p.1946-1955

2000

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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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Evaluation of clinical and laboratory features of antiphospholipid syndrome: a retrospective study of 637 patients

Lupus, 2003-01, Vol.12 (4), p.302-307

2003

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T239 Von Willebrand factor levels in patients with systemic lupus erythematosus and antiphospholipid syndrome

Clinica chimica acta, 2022-05, Vol.530, p.S176-S176

2022

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Factor XIII: novel structural and functional aspects

Auto‐ and alloantibodies against factor XIII: laboratory diagnosis and clinical consequences

Diagnosis and classification of factor XIII deficiencies

Mechanism of the irreversible inhibition of human cyclooxygenase-1 by aspirin as predicted by QM/MM calculations

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

Minimal factor XIII activity level to prevent major spontaneous bleeds

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

Neutralizing autoantibody against factor XIII A subunit resulted in severe bleeding diathesis with a fatal outcome – characterization of the antibody

Factor XIII: recommended terms and abbreviations

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

Prophylactic and perioperative replacement therapy for acquired factor XIII deficiency: a rebuttal

Severe bleeding diatheses in an elderly patient with combined type autoantibody against factor XIII A subunit; novel approach to the diagnosis and classification of anti‐factor XIII antibodies

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

Plasma clot properties in patients with a mild-to-moderate bleeding tendency of unknown cause

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

Molecular mechanism of the interaction between activated factor XIII and its glutamine donor peptide substrate

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

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

A Modified, Optimized Kinetic Photometric Assay for the Determination of Blood Coagulation Factor XIII Activity in Plasma

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

Evaluation of clinical and laboratory features of antiphospholipid syndrome: a retrospective study of 637 patients

T239 Von Willebrand factor levels in patients with systemic lupus erythematosus and antiphospholipid syndrome

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