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Clinical significance of slightly reduced von Willebrand factor activity

Polskie archiwum medycyny wewne̦trznej, 2020-03, Vol.130 (3), p.225-231

2020

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Bleeding complications after arthroscopy in a JAK2V617F-positive patient with essential thrombocythemia and acquired von Willebrand syndrome (AVWS)

International journal of hematology, 2015-04, Vol.101 (4), p.405-410

2015

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Heyde's syndrome without a decrease in large von Willebrand factor multimers: a case of intestinal bleedings reversed by valve replacement in a patient with aortic stenosis

Thrombosis and haemostasis, 2009-04, Vol.101 (4), p.773

2009

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Clinical, Biochemical and Molecular Characteristics of the Main Types of Porphyria

Advances in clinical and experimental medicine : official organ Wroclaw Medical University, 2016-03, Vol.25 (2), p.361-368

2016

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Protein Z in young survivors of ischemic stroke

Thrombosis and haemostasis, 2002-09, Vol.88 (3), p.536

2002

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Increased thrombin generation and platelet activation are associated with deficiency in high molecular weight multimers of von Willebrand factor in patients with moderate-to-severe aortic stenosis

Heart (British Cardiac Society), 2011-12, Vol.97 (24), p.2023-2028

2011

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Factor V Leiden, Prothrombin Gene G20210A Variant, and Methylenetetrahydrofolate Reductase C677T Genotype in Young Adults With Ischemic Stroke

Clinical and applied thrombosis/hemostasis, 2001-10, Vol.7 (4), p.346-350

2001

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Prevention of bleeding and hemorrhagic complications in surgical patients with inherited factor VII deficiency

Blood coagulation & fibrinolysis, 2015-04, Vol.26 (3), p.324-330

2015

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Acquired thrombotic thrombocytopenic purpura (TTP) induced by silicone breast implants in 37-year old woman

Thrombosis research, 2013-05, Vol.131 (5), p.e223-e225

2013

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Von Willebrand factor propeptide (VWFpp) — potential biomarker in inherited von Willebrand disease and acquired von Willebrand syndrome

Journal of Transfusion Medicine, 2019-12, Vol.12 (4), p.176-190

2019

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Prevalence rate for inherited thrombophilia in patients with chronic and recurrent venous leg ulceration

Wound repair and regeneration, 2011-09, Vol.19 (5), p.552-558

2011

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Porphobilinogen deaminase gene mutations in Polish patients with non-erythroid acute intermittent porphyria

Advances in clinical and experimental medicine : official organ Wroclaw Medical University, 2015-01, Vol.24 (1), p.63-68

2015

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Wykrywanie mutacji inwersyjnych (INV22 oraz INV1) w genie F8 metodą IS-PCR u polskich chorych na ciężką hemofilię A

Acta haematologica polonica, 2015-11, Vol.46 (5), p.372-377

2015

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Wykrywanie mutacji inwersyjnych (INV22 oraz INV1) w genie F8 metodą IS-PCR u polskich chorych na ciężką hemofilię A

Acta haematologica polonica, 2015-11, Vol.46 (5), p.372-377

2015

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Perioperative bridging therapy with low molecular weight heparin for patients with inherited thrombophilia and antiphospholipid syndrome on long-term acenokumarol therapy

Blood coagulation & fibrinolysis, 2011-01, Vol.22 (1), p.34-39

2011

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Polymorphisms in the factor VII gene and ischemic stroke in young adults

Blood coagulation & fibrinolysis, 2010-07, Vol.21 (5), p.442-447

2010

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Zakrzepowa plamica małopłytkowa u 3-letniego chłopca – opis przypadku

Pediatria polska, 2012-11, Vol.87 (6), p.615-620

2012

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The first case of combined coagulation factor V and coagulation factor VIII deficiency in Poland due to a novel p.Tyr135Asn missense mutation in the MCFD2 gene

Blood coagulation & fibrinolysis, 2008-09, Vol.19 (6), p.431-534

2008

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JAK2 Mutational Status, Hemostatic Risk Factors and Thrombophilic Factors in Essential Thrombocythemia (ET) Patients

Blood, 2008-11, Vol.112 (11), p.4542-4542

2008

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The first case of combined coagulation factor V and coagulation factor VIII deficiency in Poland due to a novel p.Tyr135Asn missense mutation in the MCFD2 gene

Blood coagulation & fibrinolysis, 2008-06, p.1

2008

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JAK2 mutation status, hemostatic risk factors and thrombophilic factors in essential thrombocythemia (ET) patients

Folia histochemica et cytobiologica, 2011-01, Vol.49 (2), p.267-271

2011

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JAK2 mutation status, hemostatic risk factors and thrombophilic factors in essential thrombocythemia (ET) patients

Folia histochemica et cytobiologica, 2011-07, Vol.49 (2), p.267-271

2011

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Łagodna hiperhomocysteinemia u chorych z nadpłytkowością samoistną (NS), związek z mutacją genu MTHFR i poziomem kwasu foliowego

Acta haematologica polonica, 2013-07, Vol.44 (3), p.333-339

2013

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Wtórne nowotwory u chorych z nadpłytkowością samoistną leczonych w Klinice Hematoonkologii i Transplantacji Szpiku UM w Lublinie

Acta haematologica polonica, 2012, Vol.43 (3), p.299-303

2012

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Molecular analysis of hemophilia B in Poland: 12 novel mutations of the factor IX gene

Acta biochimica polonica, 1999-01, Vol.46 (3), p.721-726

1999

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Clinical significance of slightly reduced von Willebrand factor activity

Bleeding complications after arthroscopy in a JAK2V617F-positive patient with essential thrombocythemia and acquired von Willebrand syndrome (AVWS)

Heyde's syndrome without a decrease in large von Willebrand factor multimers: a case of intestinal bleedings reversed by valve replacement in a patient with aortic stenosis

Clinical, Biochemical and Molecular Characteristics of the Main Types of Porphyria

Protein Z in young survivors of ischemic stroke

Increased thrombin generation and platelet activation are associated with deficiency in high molecular weight multimers of von Willebrand factor in patients with moderate-to-severe aortic stenosis

Factor V Leiden, Prothrombin Gene G20210A Variant, and Methylenetetrahydrofolate Reductase C677T Genotype in Young Adults With Ischemic Stroke

Prevention of bleeding and hemorrhagic complications in surgical patients with inherited factor VII deficiency

Acquired thrombotic thrombocytopenic purpura (TTP) induced by silicone breast implants in 37-year old woman

Von Willebrand factor propeptide (VWFpp) — potential biomarker in inherited von Willebrand disease and acquired von Willebrand syndrome

Prevalence rate for inherited thrombophilia in patients with chronic and recurrent venous leg ulceration

Porphobilinogen deaminase gene mutations in Polish patients with non-erythroid acute intermittent porphyria

Wykrywanie mutacji inwersyjnych (INV22 oraz INV1) w genie F8 metodą IS-PCR u polskich chorych na ciężką hemofilię A

Wykrywanie mutacji inwersyjnych (INV22 oraz INV1) w genie F8 metodą IS-PCR u polskich chorych na ciężką hemofilię A

Perioperative bridging therapy with low molecular weight heparin for patients with inherited thrombophilia and antiphospholipid syndrome on long-term acenokumarol therapy

Polymorphisms in the factor VII gene and ischemic stroke in young adults

Zakrzepowa plamica małopłytkowa u 3-letniego chłopca – opis przypadku

The first case of combined coagulation factor V and coagulation factor VIII deficiency in Poland due to a novel p.Tyr135Asn missense mutation in the MCFD2 gene

JAK2 Mutational Status, Hemostatic Risk Factors and Thrombophilic Factors in Essential Thrombocythemia (ET) Patients

The first case of combined coagulation factor V and coagulation factor VIII deficiency in Poland due to a novel p.Tyr135Asn missense mutation in the MCFD2 gene

JAK2 mutation status, hemostatic risk factors and thrombophilic factors in essential thrombocythemia (ET) patients

JAK2 mutation status, hemostatic risk factors and thrombophilic factors in essential thrombocythemia (ET) patients

Łagodna hiperhomocysteinemia u chorych z nadpłytkowością samoistną (NS), związek z mutacją genu MTHFR i poziomem kwasu foliowego

Wtórne nowotwory u chorych z nadpłytkowością samoistną leczonych w Klinice Hematoonkologii i Transplantacji Szpiku UM w Lublinie

Molecular analysis of hemophilia B in Poland: 12 novel mutations of the factor IX gene

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