Lista de obras -

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

artículo científico publicado en 2013

Alterations of blood platelet function induced by neutral proteases from human leukocytes

artículo científico publicado en 1985

Anticoagulant properties of extracellular slime substance produced by Staphylococcus epidermidis.

artículo científico publicado en 1985

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

artículo científico publicado en 2014

Characterization of a plasminogen activator secreted by cultured bovine aortic endothelial cells

scientific article published on 01 April 1982

Clinical significance of slightly reduced von Willebrand factor activity

scientific article published on 28 January 2020

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

artículo científico publicado en 2016

Cryoprecipitate of intermediate purity produced in a closed thaw-siphon system from DDAVP stimulated blood donor plasma

artículo científico publicado el 1 de enero de 1990

Degradation of glycophorin A of human erythrocytes in patients with myelo- or lymphoproliferative disorders: possible role of neutrophil proteases

artículo científico publicado en 1997

Degradation of human erythrocyte surface components by human neutrophil elastase and cathepsin G: preferential digestion of glycophorins

scientific article published on 01 August 1993

Detection of Hemophilia A carrier state

artículo científico publicado el 1 de julio de 1977

Differences between Type I Autoimmune Inhibitors of Fibrin Stabilization in Two Patients with Severe Hemorrhagic Disorder ⬇️

artículo científico publicado el 1 de mayo de 1978

Different effects of human neutrophil elastase on platelet glycoproteins IIb and IIIa of resting and stimulated platelets

artículo científico publicado en 1990

Effect of Toxic Shock Syndrome Toxin 1 on Human Platelets

artículo científico publicado en 1989

Effect of neutral proteases from blood leukocytes on human platelets

artículo científico publicado el 30 de diciembre de 1983

Effect of proteolysis on quantitation of plasma fibronectin concentration by two immunoassays (electroimmunoassay and immunoturbidimetric technique)

artículo científico publicado en 1985

Effects of human neutrophil elastase and cathepsin G on the reactivity of platelets with antiplatelet antibodies

artículo científico publicado el 1 de enero de 1995

Effects of neutral proteases from human leukocytes on structure and biological properties of human factor VIII

artículo científico publicado el 15 de julio de 1980

Factor V Leiden, prothrombin gene G20210A variant, and methylenetetrahydrofolate reductase C677T genotype in young adults with ischemic stroke.

artículo científico publicado en 2001

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.

artículo científico publicado en 2009

Human platelets release alpha-6-L-fucosyltransferase upon activation

scientific article published on 01 February 1989

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

artículo científico publicado en 2011

Isolation and some properties of factor VIII (antihemophilic factor)

artículo científico publicado el 1 de octubre de 1976

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

artículo científico publicado en 2011

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

artículo científico publicado en 1999

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

artículo científico publicado en 2011

Phenotype-genotype correlation in eight Polish patients with inherited Factor XIII deficiency: identification of three novel mutations.

artículo científico publicado en 2007

Physiochemical properties and structure of factor VIII

artículo científico publicado el 1 de enero de 1977

Plasma fibronectin concentrations in healthy and septic infants

scientific article published on 01 May 1985

Plasma fibronectin in acute leukaemias and during streptokinase therapy

artículo científico publicado en 1988

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

artículo científico publicado en 2010

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

artículo científico publicado en 2015

Prevalence of heparin cofactor II deficiency in patients with a history of venous thrombosis

scientific article published on 01 January 1996

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

scientific article published on 01 September 2011

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

artículo científico publicado en 2015

Protein Z in young survivors of ischemic stroke

artículo científico publicado en 2002

Purification and characterization of the plasminogen activator secreted by a rat brain tumor cell line in culture

scientific article published on 01 October 1981

Quinidine-induced thrombocytopenia

artículo científico publicado en 1991

Role of serpins in regulation of hemostasis

artículo científico publicado el 1 de enero de 1992

Secretory response of the vessel wall to DDAVP and venous occlusion in von Willebrand's disease

artículo científico publicado en 1994

Separation of human antihemophilic factor (AHF, factor VIII) from fibrinogen by means of defibrase

artículo científico publicado en 1975

Suppressive effect of low molecular weight fibrinogen degradation products on human and rat lymphocytes

artículo científico publicado el 1 de marzo de 1978

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.

artículo científico publicado en 2008

Venostasis but not DDAVP infusion provokes the plasma fibronectin increase

artículo científico publicado en 1990

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

artículo científico publicado en 2012

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

artículo científico publicado en 2015

Zakrzepowa plamica małopłytkowa u 3-letniego chłopca – opis przypadku

artículo científico publicado en 2012

[Evaluation of the stability of lyophilized factor IX concentrate]

scientific article published on 01 July 1985

[Platelet receptors for adhesive proteins and their clinical significance]

artículo científico publicado en 1993

[Prevalence of G20210A prothrombin gene mutation in Poland]

artículo científico publicado en 2000

[Variant of von Willebrand's disease in 3 Polish families]

artículo científico publicado en 1980

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

artículo científico publicado en 2013

Lista de obras de

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

Alterations of blood platelet function induced by neutral proteases from human leukocytes

Anticoagulant properties of extracellular slime substance produced by Staphylococcus epidermidis.

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

Characterization of a plasminogen activator secreted by cultured bovine aortic endothelial cells

Clinical significance of slightly reduced von Willebrand factor activity

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

Cryoprecipitate of intermediate purity produced in a closed thaw-siphon system from DDAVP stimulated blood donor plasma

Degradation of glycophorin A of human erythrocytes in patients with myelo- or lymphoproliferative disorders: possible role of neutrophil proteases

Degradation of human erythrocyte surface components by human neutrophil elastase and cathepsin G: preferential digestion of glycophorins

Detection of Hemophilia A carrier state

Differences between Type I Autoimmune Inhibitors of Fibrin Stabilization in Two Patients with Severe Hemorrhagic Disorder ⬇️

Different effects of human neutrophil elastase on platelet glycoproteins IIb and IIIa of resting and stimulated platelets

Effect of Toxic Shock Syndrome Toxin 1 on Human Platelets

Effect of neutral proteases from blood leukocytes on human platelets

Effect of proteolysis on quantitation of plasma fibronectin concentration by two immunoassays (electroimmunoassay and immunoturbidimetric technique)

Effects of human neutrophil elastase and cathepsin G on the reactivity of platelets with antiplatelet antibodies

Effects of neutral proteases from human leukocytes on structure and biological properties of human factor VIII

Factor V Leiden, prothrombin gene G20210A variant, and methylenetetrahydrofolate reductase C677T genotype in young adults with ischemic stroke.

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.

Human platelets release alpha-6-L-fucosyltransferase upon activation

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

Isolation and some properties of factor VIII (antihemophilic factor)

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

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

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

Phenotype-genotype correlation in eight Polish patients with inherited Factor XIII deficiency: identification of three novel mutations.

Physiochemical properties and structure of factor VIII

Plasma fibronectin concentrations in healthy and septic infants

Plasma fibronectin in acute leukaemias and during streptokinase therapy

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

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

Prevalence of heparin cofactor II deficiency in patients with a history of venous thrombosis

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

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

Protein Z in young survivors of ischemic stroke

Purification and characterization of the plasminogen activator secreted by a rat brain tumor cell line in culture

Quinidine-induced thrombocytopenia

Role of serpins in regulation of hemostasis

Secretory response of the vessel wall to DDAVP and venous occlusion in von Willebrand's disease

Separation of human antihemophilic factor (AHF, factor VIII) from fibrinogen by means of defibrase

Suppressive effect of low molecular weight fibrinogen degradation products on human and rat lymphocytes

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.

Venostasis but not DDAVP infusion provokes the plasma fibronectin increase

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

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

Zakrzepowa plamica małopłytkowa u 3-letniego chłopca – opis przypadku

[Evaluation of the stability of lyophilized factor IX concentrate]

[Platelet receptors for adhesive proteins and their clinical significance]

[Prevalence of G20210A prothrombin gene mutation in Poland]

[Variant of von Willebrand's disease in 3 Polish families]

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