Search Results - "Bykowska, Ksenia"
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Bleeding complications after arthroscopy in a JAK2V617F-positive patient with essential thrombocythemia and acquired von Willebrand syndrome (AVWS)
Published in International journal of hematology (01-04-2015)“…Acquired von Willebrand syndrome (AVWS) is an acquired bleeding disorder with clinical and laboratory features similar to those of the inherited form of the…”
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Protein Z in young survivors of ischemic stroke
Published in Thrombosis and haemostasis (01-09-2002)Get more information
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Clinical significance of slightly reduced von Willebrand factor activity
Published in Polskie archiwum medycyny wewne̦trznej (27-03-2020)“…Von Willebrand disease (VWD) is the most common congenital bleeding disorder, with a clinical presentation of mucocutaneous and surgical bleeding varying from…”
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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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Clinical, Biochemical and Molecular Characteristics of the Main Types of Porphyria
Published in Advances in clinical and experimental medicine : official organ Wroclaw Medical University (01-03-2016)“…Porphyrias are diverse disorders that arise from various inherited enzyme defects in the heme biosynthesis pathway, except for porphyria cutanea tarda (PCT),…”
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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
Published in Heart (British Cardiac Society) (01-12-2011)“…High molecular weight von Willebrand factor (vWF) multimers (HMWM) are often deficient in patients with severe aortic stenosis (AS) owing to shear…”
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Prevention of bleeding and hemorrhagic complications in surgical patients with inherited factor VII deficiency
Published in Blood coagulation & fibrinolysis (01-04-2015)“…Inherited factor VII (FVII) deficiency is a rare autosomal recessive hemorrhagic disorder. The major clinical symptoms includebleeding from the oral cavity,…”
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Acquired thrombotic thrombocytopenic purpura (TTP) induced by silicone breast implants in 37-year old woman
Published in Thrombosis research (01-05-2013)Get full text
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Prevalence rate for inherited thrombophilia in patients with chronic and recurrent venous leg ulceration
Published in Wound repair and regeneration (01-09-2011)“…The aim of the study was to determine the prevalence rate for inherited thrombophilia (IT) in patients with chronic (CVU) and recurrent venous leg ulceration…”
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Porphobilinogen deaminase gene mutations in Polish patients with non-erythroid acute intermittent porphyria
Published in Advances in clinical and experimental medicine : official organ Wroclaw Medical University (01-01-2015)“…Acute intermittent porphyria (AIP) is an metabolic disorder characterized by a partial deficiency of the porphobilinogen deaminase, the enzyme of heme…”
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Wykrywanie mutacji inwersyjnych (INV22 oraz INV1) w genie F8 metodą IS-PCR u polskich chorych na ciężką hemofilię A
Published in Acta haematologica polonica (01-11-2015)“…Hemophilia A is a genetically determined bleeding disorder, caused by deficiency, lack or dysfunction of plasma coagulation factor VIII. Approximately in…”
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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
Published in Blood coagulation & fibrinolysis (01-01-2011)“…The aim of the study is to present our own perioperative bridging therapy with low molecular weight heparin (LMWH) for surgical patients with thrombophilia on…”
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Polymorphisms in the factor VII gene and ischemic stroke in young adults
Published in Blood coagulation & fibrinolysis (01-07-2010)“…Polymorphic configurations of the coagulation factor VII gene (F7) are associated with plasma levels of FVII antigen (FVII:Ag) and FVII coagulant activity…”
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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
Published in Blood coagulation & fibrinolysis (01-09-2008)“…Congenital combined coagulation factor V and coagulation factor VIII deficiency (F5F8D) is a rare bleeding disorder due to mutations in the LMAN1 or MCFD2…”
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JAK2 Mutational Status, Hemostatic Risk Factors and Thrombophilic Factors in Essential Thrombocythemia (ET) Patients
Published in Blood (16-11-2008)“…The recently discovered JAK 2 V617F activating tyrosine-kinase mutation has been found in 50–70% of Essential Thrombocythemia (ET) patients. Increased risk of…”
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JAK2 mutation status, hemostatic risk factors and thrombophilic factors in essential thrombocythemia (ET) patients
Published in Folia histochemica et cytobiologica (01-01-2011)“…The recently discovered JAK2 V617F point mutation, found in 50-60% of ET patients, has been reported to be associated with a higher risk of thrombotic events…”
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JAK2 mutation status, hemostatic risk factors and thrombophilic factors in essential thrombocythemia (ET) patients
Published in Folia histochemica et cytobiologica (01-07-2011)“…The recently discovered JAK2 V617F point mutation, found in 50–60% of ET patients, has been reported to be associated with a higher risk of thrombotic…”
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