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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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Common large partial VWF gene deletion does not cause alloantibody formation in the Hungarian type 3 von Willebrand disease population

Journal of thrombosis and haemostasis, 2011-05, Vol.9 (5), p.945-952

2011

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P149 Case report: lymphomatoid granulomatosis transformed from CLL

Blood reviews, 2007, Vol.21, p.S134-S134

2007

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P046 The use of rotation thrombelastography in familial thrombophilia

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

2007

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O57 Autologous hematopoietic stem cell transplantation in T/0-cell non Hodgkin lymphoma. Single center experiences

Blood reviews, 2007, Vol.21, p.S84-S85

2007

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P060 Molecular genetic results of Transdanubian haemophilic patients

Blood reviews, 2007, Vol.21, p.S105-S105

2007

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P147 Multiple extranodal relapses in diffuse large B-cell lymphoma (case report)

Blood reviews, 2007, Vol.21, p.S133-S133

2007

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Two successful pregnancies following eight miscarriages in a patient with antithrombin deficiency

Gynecologic and obstetric investigation, 2006-01, Vol.61 (2), p.111

2006

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P061 Type 3 von Willebrand disease in Hungary: A partial large deletion is the most common genetic defect

Blood reviews, 2007, Vol.21, p.S105-S105

2007

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P171 Influence of favourable and unfavourable genetic prognostic markers and CD 38 expression in chronic lymphocytic leukemia on treatment free interval and overal survival. Single center experience between 2002 2006

Blood reviews, 2007, Vol.21, p.S140-S140

2007

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P202 Multidrug resistance in chronic lymphocytic leukemia

Blood reviews, 2007, Vol.21, p.S140-S140

2007

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Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene

Haemophilia : the official journal of the World Federation of Hemophilia, 2009-01, Vol.15 (1), p.267-280

2009

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Clinical phenotypes and factor VII genotype in congenital factor VII deficiency

Thrombosis and haemostasis, 2005-03, Vol.93 (3), p.481

2005

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Identification of mutations in 15 Hungarian families with hereditary protein C deficiency

British journal of haematology, 2000-10, Vol.111 (1), p.129-135

2000

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Hepatitis C virus infection associated with B-cell non-Hodgkin's lymphoma in Hungarian patients

British journal of haematology, 2000-08, Vol.110 (2), p.497-498

2000

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Molecular Biology and Clinical Manifestation of Hereditary Factor VII Deficiency

Seminars in thrombosis and hemostasis, 2000, Vol.26 (4), p.0393-0400

2000

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THE EFFECT OF ADP RECEPTOR ANTAGONISTS AND ASPIRIN ON WHOLE BLOOD PLATELET AGGREGATION MEASURED BY MULTIPLE ELECTRODE AGGREGOMETRY

Journal of thrombosis and haemostasis, 2007-07, Vol.5, p.P-T-360-P-T-360

2007

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Increased prevalence of factor V Leiden mutation in neonatal intracranial haemorrhage

European journal of pediatrics, 1998-03, Vol.157 (3), p.261-261

1998

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Karyotype complexity and VH gene status in B-cell chronic lymphocytic leukemia

Haematologica (Roma), 2006-10, Vol.91 (10), p.1430-1431

2006

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Increased incidence of monoclonal B-cell infiltrate in chronic myeloproliferative disorders

Modern pathology, 2004-12, Vol.17 (12), p.1521-1530

2004

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Current principles of diagnosis and treatment of chronic lymphocytic B-cell leukemia

Orvosi hetilap, 1998-03, Vol.139 (11), p.611

Losonczy, H

1998

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Effect of Pentosan Polysulfate on Activated Partial Thromboplastin Time, Thrombin Time, Euglobulin Clot Lysis, and on Tissue-Type Plasminogen Activator and Plasminogen Activator Inhibitor Activities in Patients with Thromboembolic Disease

Seminars in thrombosis and hemostasis, 1991-10, Vol.17 (4), p.394-398

1991

Volltextzugriff (PDF)

Variability of clinical manifestation of factor VII-deficiency in homozygous and heterozygous subjects of the European F7 gene mutation A294V

Haematologica (Roma), 2008-08, Vol.93 (8), p.1273-1275

2008

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Penile chloroma in a patient with secondary acute myeloid leukemia

European journal of haematology, 2002-05, Vol.68 (5), p.322-322

2002

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Detection of TNFα expression in the bone marrow and determination of TNFα production of peripheral blood mononuclear cells in myelodysplastic syndrome

Pathology oncology research, 2000, Vol.6 (1), p.18-23

2000

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

Common large partial VWF gene deletion does not cause alloantibody formation in the Hungarian type 3 von Willebrand disease population

P149 Case report: lymphomatoid granulomatosis transformed from CLL

P046 The use of rotation thrombelastography in familial thrombophilia

O57 Autologous hematopoietic stem cell transplantation in T/0-cell non Hodgkin lymphoma. Single center experiences

P060 Molecular genetic results of Transdanubian haemophilic patients

P147 Multiple extranodal relapses in diffuse large B-cell lymphoma (case report)

Two successful pregnancies following eight miscarriages in a patient with antithrombin deficiency

P061 Type 3 von Willebrand disease in Hungary: A partial large deletion is the most common genetic defect

P171 Influence of favourable and unfavourable genetic prognostic markers and CD 38 expression in chronic lymphocytic leukemia on treatment free interval and overal survival. Single center experience between 2002 2006

P202 Multidrug resistance in chronic lymphocytic leukemia

Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene

Clinical phenotypes and factor VII genotype in congenital factor VII deficiency

Identification of mutations in 15 Hungarian families with hereditary protein C deficiency

Hepatitis C virus infection associated with B-cell non-Hodgkin's lymphoma in Hungarian patients

Molecular Biology and Clinical Manifestation of Hereditary Factor VII Deficiency

THE EFFECT OF ADP RECEPTOR ANTAGONISTS AND ASPIRIN ON WHOLE BLOOD PLATELET AGGREGATION MEASURED BY MULTIPLE ELECTRODE AGGREGOMETRY

Increased prevalence of factor V Leiden mutation in neonatal intracranial haemorrhage

Karyotype complexity and VH gene status in B-cell chronic lymphocytic leukemia

Increased incidence of monoclonal B-cell infiltrate in chronic myeloproliferative disorders

Current principles of diagnosis and treatment of chronic lymphocytic B-cell leukemia

Effect of Pentosan Polysulfate on Activated Partial Thromboplastin Time, Thrombin Time, Euglobulin Clot Lysis, and on Tissue-Type Plasminogen Activator and Plasminogen Activator Inhibitor Activities in Patients with Thromboembolic Disease

Variability of clinical manifestation of factor VII-deficiency in homozygous and heterozygous subjects of the European F7 gene mutation A294V

Penile chloroma in a patient with secondary acute myeloid leukemia

Detection of TNFα expression in the bone marrow and determination of TNFα production of peripheral blood mononuclear cells in myelodysplastic syndrome

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