Search Results - "ŁOpaciuk, S."
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1
Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-09-2006)“…Inherited factor X deficiency (FXD) is a rare (1:1 000 000) recessive bleeding disorder. The clinical and laboratory phenotypes of FXD are poorly correlated…”
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2
Low molecular weight heparin versus acenocoumarol in the secondary prophylaxis of deep vein thrombosis
Published in Thrombosis and haemostasis (01-01-1999)“…The aim of this study was to determine the efficacy and safety of subcutaneous weight-adjusted dose low molecular weight heparin (LMWH) compared with oral…”
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3
Degradation of glycophorin A of human erythrocytes in patients with myelo‐ or lymphoproliferative disorders: possible role of neutrophil proteases
Published in British journal of haematology (01-03-1997)“…We have previously reported that glycophorin A (GPA) of human erythrocytes (carrying blood group M and N determinants) was totally digested by incubation of…”
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4
An ultrapure plasma-derived monoclonal antibody-purified factor IX concentrate (Nonafact®), results of phase III and IV clinical studies
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-05-2011)“…Nonafact®, an ultrapure, monoclonal antibody‐purified factor IX concentrate (FIX) was developed to minimize risk of thrombotic complications and viral…”
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5
Haemophilia in Poland
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-01-2006)“…The primary aim of this study was to analyse the data on 2269 haemophilic patients in the Polish National Register of Inherited Bleeding Disorders – 1953…”
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6
Consensus perspectives on surgery in haemophilia patients with inhibitors: summary statement
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-09-2004)“…Participants in an international workshop on surgery in haemophilia patients with inhibitors developed a consensus summary of the findings and conclusions of…”
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7
Alterations of blood platelet function induced by neutral proteases from human leukocytes
Published in Thrombosis research (01-06-1985)“…Washed human platelets are damaged by two neutral proteases from human leukocytes (elastase-like protease, ELP and chymotrypsin-like protease, CLP). The damage…”
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8
Factor V Leiden, prothrombin gene G20210A variant, and methylenetetrahydrofolate reductase C677T genotype in young adults with ischemic stroke
Published in Clinical and applied thrombosis/hemostasis (01-10-2001)“…Ischemic stroke in young adults is a well-known disease, but despite extensive clinical and laboratory investigations, its etiology remains unclear in…”
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9
Clinical efficacy, safety and pharmacokinetic properties of the factor VIII concentrate Haemoctin® SDH in previously treated patients with severe haemophilia A
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-09-2004)“…Clinical efficacy, safety and pharmacokinetic properties of the high‐purity double‐virus inactivated plasma‐derived factor VIII concentrate Haemoctin® SDH…”
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10
Subcutaneous low molecular weight heparin versus subcutaneous unfractionated heparin in the treatment of deep vein thrombosis: a Polish multicenter trial
Published in Thrombosis and haemostasis (06-07-1992)“…In a prospective multicenter trial, 149 consecutive patients with phlebographically proven proximal and/or distal deep vein thrombosis of the leg were randomly…”
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11
Prevalence of factor V Leiden mutation in various populations
Published in Genetic epidemiology (1997)“…Resistance to activated protein C (APC) is the most common inherited risk factor for venous thrombosis. Most cases of APC resistance are caused by the point…”
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12
Bovine platelet proteins. II. Purification of platelet fibrinogen
Published in Thrombosis et diathesis haemorrhagica (15-06-1969)Get more information
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13
Inherited thrombophilia and complications of pregnancy
Published in Polskie archiwum medycyny wewne̦trznej (2001)Get more information
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14
Inherited thrombophilia: pathogenesis, clinical and treatment aspects
Published in Polskie archiwum medycyny wewne̦trznej (01-11-2000)Get more information
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15
Monocytes of patients congenitally deficient in plasma factor XIII lack factor XIII subunit a antigen and transglutaminase activity
Published in Thrombosis and haemostasis (08-04-1988)“…Monocytes isolated from patients with severe deficiency in plasma Factor XIII of blood coagulation (FXIII) were tested for FXIII antigen and transglutaminase…”
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16
Venostasis but not DDAVP infusion provokes the plasma fibronectin increase
Published in Thrombosis and haemostasis (22-10-1990)“…Plasma fibronectin (pFN), von Willebrand factor antigen (vWf:Ag), factor VIII procoagulant activity, fibrinogen, euglobulin lysis time (ELT) and hematocrit…”
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17
Different effects of human neutrophil elastase on platelet glycoproteins IIb and IIIa of resting and stimulated platelets
Published in Thrombosis and haemostasis (13-08-1990)“…The effect of human neutrophil elastase (HNE) on the structure and receptor activity of platelet glycoprotein IIb/IIIa complex was studied. Resting platelets,…”
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18
Prevalence of G20210A prothrombin gene mutation in Poland
Published in Polskie archiwum medycyny wewne̦trznej (01-11-2000)“…The G20210A mutation of the prothrombin (PT) gene has recently been identified as a risk factor for venous thromboembolism (VTE). This mutation was shown to be…”
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19
Effects of human neutrophil elastase and cathepsin G on the reactivity of platelets with antiplatelet antibodies
Published in Acta haematologica polonica (1995)“…Two human neutrophil serine proteases, elastase (HNE) and cathepsin G (CathG), are known to change the structure and hemostatic function of platelet surface…”
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Subcellular distribution of fibrinogen and factor XIII in human blood platelets
Published in Thrombosis research (1976)Get more information
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