Search Results - "Dobrotova Miroslava"

Comparison of clinical phenotype with genetic and laboratory results in 31 patients with congenital dysfibrinogenemia in northern Slovakia by Simurda, Tomas, Zolkova, Jana, Kolkova, Zuzana, Loderer, Dusan, Dobrotova, Miroslava, Skornova, Ingrid, Brunclíkova, Monika, Grendar, Marian, Lasabova, Zora, Stasko, Jan, Kubisz, Peter

“…Congenital dysfibrinogenemia (CD) is a rare disorder of hemostasis. The majority of cases are caused by heterozygous missense mutations in one of the three…”
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Apixaban - Metabolism, Pharmacologic Properties and Drug Interactions by Kubisz, Peter, Stanciakova, Lucia, Dobrotova, Miroslava, Samos, Matej, Mokan, Marian, Stasko, Jan

“…Apixaban is an oral, potent, highly selective, reversible and direct inhibitor of activated coagulation factor X, that is the end point of the intrinsic and…”
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How can Secondary Thromboprophylaxis in High-Risk Pregnant Patients be Improved? by Stanciakova, Lucia, Dobrotova, Miroslava, Holly, Pavol, Zolkova, Jana, Vadelova, Lubica, Skornova, Ingrid, Ivankova, Jela, Samos, Matej, Bolek, Tomas, Grendar, Marian, Danko, Jan, Kubisz, Peter, Stasko, Jan

“…Low-molecular-weight heparin (LMWH) is suggested for thromboprophylaxis in pregnant women with previous venous thromboembolism (VTE). Anyway, there is only…”
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Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory and Genetic Testing in Rare Bleeding Disorders with Life-Threatening Clinical Manifestations and Challenging Management by Simurda, Tomas, Asselta, Rosanna, Zolkova, Jana, Brunclikova, Monika, Dobrotova, Miroslava, Kolkova, Zuzana, Loderer, Dusan, Skornova, Ingrid, Hudecek, Jan, Lasabova, Zora, Stasko, Jan, Kubisz, Peter

“…Congenital fibrinogen disorders are rare pathologies of the hemostasis, comprising quantitative (afibrinogenemia, hypofibrinogenemia) and qualitative…”
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A Novel Nonsense Mutation in FGB (c.1421G>A; p.Trp474Ter) in the Beta Chain of Fibrinogen Causing Hypofibrinogenemia with Bleeding Phenotype by Simurda, Tomas, Vilar, Rui, Zolkova, Jana, Ceznerova, Eliska, Kolkova, Zuzana, Loderer, Dusan, Neerman-Arbez, Marguerite, Casini, Alessandro, Brunclikova, Monika, Skornova, Ingrid, Dobrotova, Miroslava, Grendar, Marian, Stasko, Jan, Kubisz, Peter

“…Congenital hypofibrinogenemia is a rare bleeding disorder characterized by a proportional decrease of functional and antigenic fibrinogen levels…”
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At-risk Pregnant Woman with Sticky Platelet Syndrome, Previous Recurrent Preeclampsia, and Current Proteinuria - A Rare Experience by Stančiaková, Lucia, Dobrotová, Miroslava, Ivanková, Jela, Škorňová, Ingrid, Bolek, Tomáš, Brunclíková, Monika, Samoš, Matej, Danko, Ján, Škereňová, Mária, Kubisz, Peter, Staško, Ján

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Association of Genetic Variability in Selected Genes with Platelet Hyperaggregability and Arterial Thrombosis by Brunclikova Monika, Ivankova Jela, Skerenova, Maria, Simurda Tomas, Stanciakova Lucia, Skornova Ingrid, Sterankova Miroslava, Zolkova Jana, Dobrotova Miroslava, Pavol, Holly, Kubisz, Peter, Stasko, Jan

“…Introduction: Inherited platelet hyperaggregability, so called “Sticky platelet syndrome” (SPS), is a prothrombotic platelet disorder. The syndrome contributes…”
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Monitoring of dabigatran therapy using Hemoclot® Thrombin Inhibitor assay in patients with atrial fibrillation by Samoš, Matej, Stančiaková, Lucia, Ivanková, Jela, Staško, Ján, Kovář, František, Dobrotová, Miroslava, Galajda, Peter, Kubisz, Peter, Mokáň, Marián

“…Dabigatran, a new direct thrombin inhibitor, achieves strong anticoagulation that is more predictable than warfarin. Nevertheless, a patient on dabigatran…”
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Multimer Analysis of Von Willebrand Factor in Von Willebrand Disease with a Hydrasys Semi-Automatic Analyzer-Single-Center Experience by Skornova, Ingrid, Simurda, Tomas, Stasko, Jan, Zolkova, Jana, Sokol, Juraj, Holly, Pavol, Dobrotova, Miroslava, Plamenova, Ivana, Hudecek, Jan, Brunclikova, Monika, Stryckova, Alena, Kubisz, Peter

“…von Willebrand disease (VWD) is reportedly the most common inherited bleeding disorder. This disorder develops as a result of defects and/or deficiency of the…”
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DNA Polymorphisms in Pregnant Women with Sticky Platelet Syndrome by Stančiaková, Lucia, Žolková, Jana, Vadelová, Ľubica, Hornáková, Andrea, Kolková, Zuzana, Vážan, Martin, Dobrotová, Miroslava, Hollý, Pavol, Jedináková, Zuzana, Grendár, Marián, Bolek, Tomáš, Samoš, Matej, Biringer, Kamil, Danko, Ján, Burjanivová, Tatiana, Lasabová, Zora, Kubisz, Peter, Staško, Ján

“…Sticky platelet syndrome (SPS) is a thrombophilia caused by the increased aggregability of platelets in response to the addition of low concentrations of…”
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How Can Rotational Thromboelastometry as a Point-of-Care Method Be Useful for the Management of Secondary Thromboprophylaxis in High-Risk Pregnant Patients? by Stanciakova, Lucia, Dobrotova, Miroslava, Holly, Pavol, Zolkova, Jana, Vadelova, Lubica, Skornova, Ingrid, Ivankova, Jela, Bolek, Tomas, Samos, Matej, Grendar, Marian, Danko, Jan, Kubisz, Peter, Stasko, Jan

“…Thromboprophylaxis with low-molecular-weight heparin (LMWH) for patients with a history of venous thromboembolism (VTE) is suggested. Rotational…”
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Long-term secondary prophylaxis with recombinant activated factor VII (rFVIIa) in haemophilia A with inhibitors: a case report by Kubisz, Peter, Plamenová, Ivana, Stasko, Ján, Dobrotová, Miroslava, Hollý, Pavol

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in vitro testing of chemoresistance in leukaemic patients by Hatok, Jozef, Tatiana MatákovÃ, Juraj Chudej, Ján StaÅ¡ko, Miroslava DobrotovÃ, DuÅ¡an Dobrota, Peter Račay

“…The fact that leukaemic cells are primarily or secondarily resistant to cytostatics is a serious phenomenon, which leads to the failure of chemotherapy of…”
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Perioperative Monitoring with Rotational Thromboelastometry in a Severe Hemophilia A Patient Undergoing Elective Ankle Surgery by Simurda, Tomas, Drotarova, Miroslava, Skornova, Ingrid, Dobrotova, Miroslava, Brunclikova, Monika, Necas, Libor, Cibula, Zoltan, Kubisz, Peter, Stasko, Jan

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Perioperative Coagulation Management in a Patient with Congenital Afibrinogenemia during Revision Total Hip Arthroplasty by Simurda, Tomas, Kubisz, Peter, Dobrotova, Miroslava, Necas, Libor, Stasko, Jan

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Variability of GP6 gene in patients with sticky platelet syndrome and deep venous thrombosis and/or pulmonary embolism by Kotuličová, Daniela, Chudý, Peter, Škereňová, Mária, Ivanková, Jela, Dobrotová, Miroslava, Kubisz, Peter

“…The GP6 gene encodes the GPVI, a crucial platelet membrane glycoprotein, for adequate platelet activation, adhesion and aggregation. The objectives of the…”
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Yes or no for secondary prophylaxis in afibrinogenemia? by Simurda, Tomas, Stanciakova, Lucia, Stasko, Jan, Dobrotova, Miroslava, Kubisz, Peter

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Heterogeneity of Genotype-Phenotype in Congenital Hypofibrinogenemia-A Review of Case Reports Associated with Bleeding and Thrombosis by Brunclikova, Monika, Simurda, Tomas, Zolkova, Jana, Sterankova, Miroslava, Skornova, Ingrid, Dobrotova, Miroslava, Kolkova, Zuzana, Loderer, Dusan, Grendar, Marian, Hudecek, Jan, Stasko, Jan, Kubisz, Peter

“…Congenital fibrinogen disorders are diseases associated with a bleeding tendency; however, there are also reports of thrombotic events. Fibrinogen plays a role…”
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Congenital afibrinogenemia: from etiopathogenesis to challenging clinical management by Stanciakova, Lucia, Kubisz, Peter, Dobrotova, Miroslava, Stasko, Jan

“…Congenital afibrinogenemia belongs to the group of autosomal recessive bleeding disorders and represents the absolute deficiency of fibrinogen detected by an…”
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Recombinant activated factor VII as an additional agent in the management of bleeding in patients with chemotherapy-induced thrombocytopenia by Hollý, Pavol, Lisá, Lenka, Plameňová, Ivana, Dobrotová, Miroslava, Kubisz, Peter

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