Tomáš Šimurda

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

Tomáš Šimurda, Jana Žolková, Zuzana Sňahničanová et al. · International Journal of Molecular Sciences · 2017 · 32 citations · Full text

Comparison of clinical phenotype with genetic and laboratory results in 31 patients with congenital dysfibrinogenemia in northern Slovakia

Tomáš Šimurda, Jana Žolková, Zuzana Kolková et al. · International Journal of Hematology · 2020 · 29 citations

Genetic Disorder, Inherited Metabolic Disease, Hematology +11

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

Tomáš Šimurda, R. Vilar, Jana Žolková et al. · Biomedicines · 2020 · 29 citations · Full text

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

Juraj Sokol, Mária Škereňová, Jela Ivanková et al. · Clinical and Applied Thrombosis/Hemostasis · 2018 · 26 citations · Full text

Phenotypic Variation, Vascular Disease, Genetics +28

Obstetrical complications in hereditary fibrinogen disorders: the Fibrinogest study

Justine Hugon‐Rodin, Camille Carrière, S. Claeyssens et al. · Journal of Thrombosis and Haemostasis · 2023 · 21 citations · Full text

Fibrinogest Study, Gynecology, Maternal Health +4