Search Results - "Bykowska, Ksenia"

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    Clinical significance of slightly reduced von Willebrand factor activity by Bykowska, Ksenia, Ceglarek, Bernadeta

    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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    Journal Article
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    Clinical, Biochemical and Molecular Characteristics of the Main Types of Porphyria by Szlendak, Urszula, Bykowska, Ksenia, Lipniacka, Agnieszka

    “…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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    Prevention of bleeding and hemorrhagic complications in surgical patients with inherited factor VII deficiency by Wiszniewski, Adam, Szczepanik, Andrzej, Misiak, Andrzej, Bykowska, Ksenia, Szopiński, Piotr

    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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    Prevalence rate for inherited thrombophilia in patients with chronic and recurrent venous leg ulceration by Wiszniewski, Adam, Bykowska, Ksenia, Bilski, Radoslaw, Jaśkowiak, Wojciech, Proniewski, Jacek

    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 by Szlendak, Urszula, Lipniacka, Agnieszka, Bianketti, Jolanta, Podolak-Dawidziak, Maria, Bykowska, Ksenia

    “…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 by Odnoczko, Edyta, Stefańska-Windyga, Ewa, Baran, Beata, Górska-Kosicka, Magdalena, Sowińska, Joanna, Bykowska, Ksenia, Windyga, Jerzy

    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 by Wiszniewski, Adam, Szopiński, Piotr, Ratajczak, Jerzy, Bilski, Radosław, Bykowska, Ksenia

    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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    Journal Article
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    Polymorphisms in the factor VII gene and ischemic stroke in young adults by Lopaciuk, Stanislaw, Windyga, Jerzy, Watala, Cezary W, Bykowska, Ksenia, Pietrucha, Tadeusz, Kwiecinski, Hubert, Czlonkowska, Anna, Kuczynska-Zardzewialy, Arleta, Jackson, Audrey A, Carew, Josephine A, Bauer, Kenneth A

    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 by Ivaskevicius, Vytautas, Windyga, Jerzy, Baran, Beata, Bykowska, Ksenia, Daugela, Laurynas, Watzka, Matthias, Seifried, Erhard, Oldenburg, Johannes

    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 by Sokolowska, Bozena, Nowaczynska, Aleksandra, Bykowska, Ksenia, Chocholowska, Sylwia, Wejksza, Katarzyna, Walter-Cronack, Adam, Kandefer-Szerszen, Martyna, Gromek, Tomasz, Kowalska, M. Anna, Dmoszynska, Anna

    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 by Anna Dmoszyńska, Martyna Kandefer-Szerszeń, Anna M. Kowalska, Tomasz Gromek, Adam Walter-Croneck, Katarzyna Wejksza, Sylwia Chocholska, Ksenia Bykowska, Aleksandra Nowaczyńska, Bożena Sokołowska

    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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    Journal Article