Association of Genetic Variability in Selected Genes in Patients With Deep Vein Thrombosis and Platelet Hyperaggregability

por Sokol, Juraj, Skerenova, Maria, Ivankova, Jela, Simurda, Tomas, Stasko, Jan
Publicado 2018

Glycoprotein VI Gene Variants Affect Pregnancy Loss in Patients With Platelet Hyperaggregability

por Sokol, Juraj, Skerenova, Maria, Biringer, Kamil, Simurda, Tomas, Kubisz, Peter, Stasko, Jan
Publicado 2018

Basic Principles of Rotational Thromboelastometry (ROTEM(®)) and the Role of ROTEM—Guided Fibrinogen Replacement Therapy in the Management of Coagulopathies

por Drotarova, Miroslava, Zolkova, Jana, Belakova, Kristina Maria, Brunclikova, Monika, Skornova, Ingrid, Stasko, Jan, Simurda, Tomas
Publicado 2023

Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders

por Simurda, Tomas, Zolkova, Jana, Snahnicanova, Zuzana, Loderer, Dusan, Skornova, Ingrid, Sokol, Juraj, Hudecek, Jan, Stasko, Jan, Lasabova, Zora, Kubisz, Peter
Publicado 2017

Genetic Variants in the FGB and FGG Genes Mapping in the Beta and Gamma Nodules of the Fibrinogen Molecule in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombo...

por Simurda, Tomas, Brunclikova, Monika, Asselta, Rosanna, Caccia, Sonia, Zolkova, Jana, Kolkova, Zuzana, Loderer, Dusan, Skornova, Ingrid, Hudecek, Jan, Lasabova, Zora, Stasko, Jan, Kubisz, Peter
Publicado 2020

Multimer Analysis of Von Willebrand Factor in Von Willebrand Disease with a Hydrasys Semi-Automatic Analyzer—Single-Center Experience

por Skornova, Ingrid, Simurda, Tomas, Stasko, Jan, Zolkova, Jana, Sokol, Juraj, Holly, Pavol, Dobrotova, Miroslava, Plamenova, Ivana, Hudecek, Jan, Brunclikova, Monika, Stryckova, Alena, Kubisz, Peter
Publicado 2021

Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory and Genetic Testing in Rare Bleeding Disorders with Life-Threatening Clinical Manifestations and Challenging Managemen...

por Simurda, Tomas, Asselta, Rosanna, Zolkova, Jana, Brunclikova, Monika, Dobrotova, Miroslava, Kolkova, Zuzana, Loderer, Dusan, Skornova, Ingrid, Hudecek, Jan, Lasabova, Zora, Stasko, Jan, Kubisz, Peter
Publicado 2021

Heterogeneity of Genotype–Phenotype in Congenital Hypofibrinogenemia—A Review of Case Reports Associated with Bleeding and Thrombosis

por Brunclikova, Monika, Simurda, Tomas, Zolkova, Jana, Sterankova, Miroslava, Skornova, Ingrid, Dobrotova, Miroslava, Kolkova, Zuzana, Loderer, Dusan, Grendar, Marian, Hudecek, Jan, Stasko, Jan, Kubisz, Peter
Publicado 2022

Detection of Unknown and Rare Pathogenic Variants in Antithrombin, Protein C and Protein S Deficiency Using High-Throughput Targeted Sequencing

por Vrtel, Petr, Slavik, Ludek, Vodicka, Radek, Stellmachova, Julia, Prochazka, Martin, Prochazkova, Jana, Ulehlova, Jana, Rohon, Peter, Simurda, Tomas, Stasko, Jan, Martinkova, Ivana, Vrtel, Radek
Publicado 2022

A Novel Nonsense Mutation in FGB (c.1421G>A; p.Trp474Ter) in the Beta Chain of Fibrinogen Causing Hypofibrinogenemia with Bleeding Phenotype

por 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
Publicado 2020

A Functional Assay for the Determination of Heparin-Induced Thrombocytopenia via Flow Cytometry

por Skornova, Ingrid, Simurda, Tomas, Stanciakova, Lucia, Lauko, Viliam, Holly, Pavol, Samos, Matej, Bolek, Tomas, Schnierer, Martin, Drotarova, Miroslava, Belakova, Kristina Maria, Sokol, Juraj, Stasko, Jan, Mokan, Marian, Gumulec, Jaroslav, Chrastinova, Leona
Publicado 2023