Publications by authors named "Tomas Simurda"

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A novel pathogenic variant in the fibrinogen gamma chain gene p.Glu275Lys causes congenital hypofibrinogenemia.
Miroslava Drotarova, Rosanna Asselta, Sonia Caccia, Ingrid Skornova, Jana Zolkova, Tomas Simurda

Blood Coagul Fibrinolysis· July 2025

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Selected and Gene Polymorphisms in Patients with Migraine and Sticky Platelet Syndrome.
Tomas Simurda, Kristina Maria Belakova, Jan Stasko, Maria Skerenova, Jela Ivankova

Clin Appl Thromb Hemost· July 2025

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Perioperative Monitoring with Rotational Thromboelastometry in a Severe Hemophilia A Patient Undergoing Elective Ankle Surgery.
Tomas Simurda, Miroslava Drotarova, Ingrid Skornova, Miroslava Dobrotova, Monika Brunclikova

Semin Thromb Hemost· March 2024

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Diagnostic value of clot formation parameters determined by rotational thromboelastometry in 63 patients with congenital dysfibrinogenemia.
Tomas Simurda, Rita Marchi, Alessandro Casini, Marguerite Neerman-Arbez, Miroslava Drotarova

Blood Coagul Fibrinolysis· March 2024

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Basic Principles of Rotational Thromboelastometry (ROTEM) and the Role of ROTEM-Guided Fibrinogen Replacement Therapy in the Management of Coagulopathies.
Miroslava Drotarova, Jana Zolkova, Kristina Maria Belakova, Monika Brunclikova, Ingrid Skornova, Tomas Simurda

Diagnostics (Basel)· October 2023

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A Functional Assay for the Determination of Heparin-Induced Thrombocytopenia via Flow Cytometry.
Ingrid Skornova, Tomas Simurda, Lucia Stanciakova, Viliam Lauko, Pavol Holly

Diagnostics (Basel)· September 2023

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Obstetrical complications in hereditary fibrinogen disorders: the Fibrinogest study.
Justine Hugon-Rodin, Camille Carrière, Ségolène Claeyssens, Nathalie Trillot, Nicolas Drillaud, Tomas Simurda

J Thromb Haemost· August 2023

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Detection of Unknown and Rare Pathogenic Variants in Antithrombin, Protein C and Protein S Deficiency Using High-Throughput Targeted Sequencing.
Petr Vrtel, Ludek Slavik, Radek Vodicka, Julia Stellmachova, Martin Prochazka, Tomas Simurda

Diagnostics (Basel)· April 2022

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Heterogeneity of Genotype-Phenotype in Congenital Hypofibrinogenemia-A Review of Case Reports Associated with Bleeding and Thrombosis.
Monika Brunclikova, Tomas Simurda, Jana Zolkova, Miroslava Sterankova, Ingrid Skornova

J Clin Med· February 2022

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Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory and Genetic Testing in Rare Bleeding Disorders with Life-Threatening Clinical Manifestations and Challenging Management.
Tomas Simurda, Rosanna Asselta, Jana Zolkova, Monika Brunclikova, Miroslava Dobrotova

Diagnostics (Basel)· November 2021

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Multimer Analysis of Von Willebrand Factor in Von Willebrand Disease with a Hydrasys Semi-Automatic Analyzer-Single-Center Experience.
Ingrid Skornova, Tomas Simurda, Jan Stasko, Jana Zolkova, Juraj Sokol

Diagnostics (Basel)· November 2021

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Use of Fibrinogen Determination Methods in Differential Diagnosis of Hypofibrinogenemia and Dysfibrinogenemia.
Ingrid Skornova, Tomas Simurda, Jan Stasko, Denis Horvath, Jana Zolkova

Clin Lab· April 2021

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A Novel Nonsense Mutation in (c.1421G>A; p.Trp474Ter) in the Beta Chain of Fibrinogen Causing Hypofibrinogenemia with Bleeding Phenotype.
Tomas Simurda, Rui Vilar, Jana Zolkova, Eliska Ceznerova, Zuzana Kolkova

Biomedicines· December 2020

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Congenital hypofibrinogenemia associated with a novel heterozygous nonsense mutation in the globular C-terminal domain of the γ-chain (p.Glu275Stop).
Tomas Simurda, Sonia Caccia, Rosanna Asselta, Jana Zolkova, Jan Stasko

J Thromb Thrombolysis· July 2020

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Genetic Background of von Willebrand Disease: History, Current State, and Future Perspectives.
Jana Zolkova, Juraj Sokol, Tomas Simurda, Lubica Vadelova, Zuzana Snahnicanova

Semin Thromb Hemost· June 2020

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Comparison of clinical phenotype with genetic and laboratory results in 31 patients with congenital dysfibrinogenemia in northern Slovakia.
Tomas Simurda, Jana Zolkova, Zuzana Kolkova, Dusan Loderer, Miroslava Dobrotova

Int J Hematol· June 2020

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Genetic Variants in the and Genes Mapping in the Beta and Gamma Nodules of the Fibrinogen Molecule in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype.
Tomas Simurda, Monika Brunclikova, Rosanna Asselta, Sonia Caccia, Jana Zolkova

Int J Mol Sci· June 2020

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Perioperative management of a severe congenital hypofibrinogenemia with thrombotic phenotype.
Tomas Simurda, Alessandro Casini, Jan Stasko, Jan Hudecek, Ingrid Skornova

Thromb Res· April 2020

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Glycoprotein VI Gene Variants Affect Pregnancy Loss in Patients With Platelet Hyperaggregability.
Juraj Sokol, Maria Skerenova, Kamil Biringer, Tomas Simurda, Peter Kubisz

Clin Appl Thromb Hemost· December 2018

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Association of Genetic Variability in Selected Genes in Patients With Deep Vein Thrombosis and Platelet Hyperaggregability.
Juraj Sokol, Maria Skerenova, Jela Ivankova, Tomas Simurda, Jan Stasko

Clin Appl Thromb Hemost· October 2018

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Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders.
Tomas Simurda, Jana Zolkova, Zuzana Snahnicanova, Dusan Loderer, Ingrid Skornova

Int J Mol Sci· December 2017

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Successful Use of a Highly Purified Plasma von Willebrand Factor Concentrate Containing Little FVIII for the Long-Term Prophylaxis of Severe (Type 3) von Willebrand's Disease.
Tomas Simurda, Miroslava Dobrotova, Ingrid Skornova, Juraj Sokol, Peter Kubisz

Semin Thromb Hemost· September 2017

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Progress in the Understanding of Sticky Platelet Syndrome.
Juraj Sokol, Maria Skerenova, Zuzana Jedinakova, Tomas Simurda, Ingrid Skornova

Semin Thromb Hemost· February 2017

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

Semin Thromb Hemost· September 2016

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Fibrinogen Martin: A Novel Mutation in FGB (Gln180Stop) Causing Congenital Afibrinogenemia.
Tomas Simurda, Zuzana Snahnicanova, Dusan Loderer, Juraj Sokol, Jan Stasko

Semin Thromb Hemost· June 2016

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