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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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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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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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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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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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Hepatitis C virus presumably associated bilateral consecutive anterior ischemic optic neuropathy

European journal of ophthalmology, 2008-03, Vol.18 (2), p.313-315

2008

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Anti‐factor V auto‐antibody in the plasma and platelets of a patient with repeated gastrointestinal bleeding

Journal of thrombosis and haemostasis, 2003-05, Vol.1 (5), p.943-949

2003

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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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P163 Sequential and comparative Zap-70 and CD38 analysis in chronic lymphoid leukemia patients

Blood reviews, 2007, Vol.21, p.S137-S138

2007

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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

2001

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High prevalence of factor V Leiden mutation and 20210A prothrombin variant in Hungary

Thrombosis and haemostasis, 1999-04, Vol.81 (4), p.660

1999

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Val34Leu polymorphism of plasma factor XIII: biochemistry and epidemiology in familial thrombophilia

Blood, 2000-10, Vol.96 (7), p.2479-2486

2000

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Identification of novel germline mutations in the VHL gene in Hungarian von Hippel‐Lindau patients

Acta ophthalmologica (Oxford, England), 2011-09, Vol.89 (s248), p.0-0

2011

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Association of ANCA-associated vasculitis-rheumatoid arthritis overlap syndrome in four patients: Rituximab may be the right choice?

Autoimmunity (Chur, Switzerland), 2012-06, Vol.45 (4), p.304-309

2012

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Attempted Suicide With Pilocarpine Eyedrops

American journal of ophthalmology, 1995-09, Vol.120 (3), p.399-400

1995

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The platelet insulin receptor: Detection, partial characterization, and search for a function

Biochemical and biophysical research communications, 1988-12, Vol.157 (3), p.1190-1196

1988

Volltextzugriff (PDF)

Trombophilic screening for nonarteritic anterior ischemic optic neuropathy

Graefe's archive for clinical and experimental ophthalmology, 2006-01, Vol.244 (1), p.3-8

2006

Volltextzugriff (PDF)

Low molecular weight heparin as thromboprophylaxis in familial thrombophilia during the whole period of pregnancy

Thrombosis and haemostasis, 1996, Vol.76 (1), p.128

1996

Volltextzugriff (PDF)

Variable response of Hermansky-Pudlak syndrome to prophylactic administration of 1-desamino 8D-arginine in subsequent pregnancies

European journal of obstetrics & gynecology and reproductive biology, 2002-09, Vol.104 (2), p.165

2002

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Low Molecular Weight Heparin as Thromboprophylaxis Throughout Pregnancy in Heritable Thrombophilic Women

Clinical and applied thrombosis/hemostasis, 1999-07, Vol.5 (3), p.198-199

1999

Volltextzugriff (PDF)

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

Blood coagulation & fibrinolysis, 1991-12, Vol.2 (6), p.775-778

1991

Volltextzugriff (PDF)

HODGKIN'S DISEASE AND MEMORY LOSS: ANOTHER CASE OF THE OPHELIA SYNDROME

British journal of haematology, 1990-02, Vol.74 (2), p.232-232

1990

Volltextzugriff (PDF)

Targeting platelets containing electro-encapsulated iloprost to balloon injured aorta in rats

Thrombosis and haemostasis, 1995-03, Vol.73 (3), p.535

1995

Volltextzugriff (PDF)

Behçet's Disease in a Patient With Myelodysplastic Syndrome

Clinical lymphoma & myeloma, 2009-12, Vol.9 (6), p.459-461

2009

Volltextzugriff (PDF)

Inhibition of platelet recruitment to arterial lesions by predeposition of platelets containing encapsulated iloprost

Thrombosis and haemostasis, 1994-10, Vol.72 (4), p.604

1994

Volltextzugriff (PDF)

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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

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

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

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

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

Hepatitis C virus presumably associated bilateral consecutive anterior ischemic optic neuropathy

Anti‐factor V auto‐antibody in the plasma and platelets of a patient with repeated gastrointestinal bleeding

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

P163 Sequential and comparative Zap-70 and CD38 analysis in chronic lymphoid leukemia patients

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

High prevalence of factor V Leiden mutation and 20210A prothrombin variant in Hungary

Val34Leu polymorphism of plasma factor XIII: biochemistry and epidemiology in familial thrombophilia

Identification of novel germline mutations in the VHL gene in Hungarian von Hippel‐Lindau patients

Association of ANCA-associated vasculitis-rheumatoid arthritis overlap syndrome in four patients: Rituximab may be the right choice?

Attempted Suicide With Pilocarpine Eyedrops

The platelet insulin receptor: Detection, partial characterization, and search for a function

Trombophilic screening for nonarteritic anterior ischemic optic neuropathy

Low molecular weight heparin as thromboprophylaxis in familial thrombophilia during the whole period of pregnancy

Variable response of Hermansky-Pudlak syndrome to prophylactic administration of 1-desamino 8D-arginine in subsequent pregnancies

Low Molecular Weight Heparin as Thromboprophylaxis Throughout Pregnancy in Heritable Thrombophilic Women

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

HODGKIN'S DISEASE AND MEMORY LOSS: ANOTHER CASE OF THE OPHELIA SYNDROME

Targeting platelets containing electro-encapsulated iloprost to balloon injured aorta in rats

Behçet's Disease in a Patient With Myelodysplastic Syndrome

Inhibition of platelet recruitment to arterial lesions by predeposition of platelets containing encapsulated iloprost

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