Výsledky vyhľadávania
- A Novel Nonsense Mutation in FGB (c.1421G>A; p.Trp474Ter) in the Beta Chain of Fibrinogen Causing Hypofibrinogenemia with Bleeding Phenotype / Simurda T., Vilar R., Zolkova J. et al. . Biomedicines . - 2020 Dec 13;8(12):605 [Dokument nie je vo fonde knižnice]
- Afibrinogenémia a dysfibrinogenémie / Tomáš Šimurda ... [et al.] . Vaskulárna medicína. - ISSN 1338-0206 . - Roč. 7, č. 2 (2015), s. 78-80 : ilustr., fareb. obr.
- C 3098
- Association of Genetic Variability in Selected Genes in Patients With Deep Vein Thrombosis and Platelet Hyperaggregability / Sokol J. ... [et al.] . Clinical and applied thrombosis/hemostasis . - Vol. 24, no. 7 (2018), s. 1027-1032 [Dokument nie je vo fonde knižnice]
- Comparison of clinical phenotype with genetic and laboratory results in 31 patients with congenital dysfibrinogenemia in northern Slovakia / Simurda T., Zolkova J., Kolkova Z. et al. . International journal of hematology . - 2020 Jun;111(6):795-802 [Dokument nie je vo fonde knižnice]
- Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory and Genetic Testing in Rare Bleeding Disorders with Life-Threatening Clinical Manifestations and Challenging Management / Simurda T., Zolkova J. et al. . Diagnostics (Basel, Switzerland) . - Vol. 11, no. 11 (2021), s. 2140 [Dokument nie je vo fonde knižnice]
- Congenital hypofibrinogenemia associated with a novel heterozygous nonsense mutation in the globular C-terminal domain of the γ-chain (p.Glu275Stop) / Simurda T. et al. . J Thromb Thrombolysis . - 2020 Jul;50(1):233-236 [Dokument nie je vo fonde knižnice]
- Diagnosis and management of von Willebrand disease in Slovakia / Kubisz P. ... [et al.] . Annals of blood . - Vol. 3 (2018), s.9 [Dokument nie je vo fonde knižnice]
- Diagnostika vrodených krvácavých porúch sekundárnej hemostázy: jednoduchý sprievodca pre bežné klinické laboratóriá / Tomáš Šimurda ... [et al.] . Newslab : časopis laboratórnej medicíny. - ISSN 1338-9661 . - Roč. 7, č. 2 (2016), s. 98-101 : ilustr., obr., tab.
- C 3151
- Genetic Background of von Willebrand Disease: History, Current State, and Future Perspectives / Zolkova J., Sokol J., Simurda T. et al. . Seminars in thrombosis and hemostasis . - Vol. 46, no. 4 (2020), s. 484-500 [Dokument nie je vo fonde knižnice]
- 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 Thrombotic Phenotype / Simurda T., Brunclikova M., Asselta R. et al. . International journal of molecular sciences . - 2020 Jul; 21(13): 4616 [Dokument nie je vo fonde knižnice]