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Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory and Genetic Testing in Rare Bleeding Disorders with Life-Threatening Clinical Manifestations and Challenging Management.
Simurda T, Asselta R, Zolkova J, Brunclikova M, Dobrotova M, Kolkova Z, Loderer D, Skornova I, Hudecek J, Lasabova Z, Stasko J, Kubisz P. Simurda T, et al. Among authors: zolkova j. Diagnostics (Basel). 2021 Nov 19;11(11):2140. doi: 10.3390/diagnostics11112140. Diagnostics (Basel). 2021. PMID: 34829490 Free PMC article. Review.
Congenital hypofibrinogenemia associated with a novel heterozygous nonsense mutation in the globular C-terminal domain of the γ-chain (p.Glu275Stop).
Simurda T, Caccia S, Asselta R, Zolkova J, Stasko J, Skornova I, Snahnicanova Z, Loderer D, Lasabova Z, Kubisz P. Simurda T, et al. Among authors: zolkova j. J Thromb Thrombolysis. 2020 Jul;50(1):233-236. doi: 10.1007/s11239-019-01991-x. J Thromb Thrombolysis. 2020. PMID: 31712947 Free article. No abstract available.
Type 2 Diabetes, Atrial Fibrillation, and Direct Oral Anticoagulation.
Prídavková D, Samoš M, Bolek T, Škorňová I, Žolková J, Kubisz P, Staško J, Mokáň M. Prídavková D, et al. Among authors: zolkova j. J Diabetes Res. 2019 Dec 6;2019:5158308. doi: 10.1155/2019/5158308. eCollection 2019. J Diabetes Res. 2019. PMID: 31886279 Free PMC article. Review.
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, Caccia S, Zolkova J, Kolkova Z, Loderer D, Skornova I, Hudecek J, Lasabova Z, Stasko J, Kubisz P. Simurda T, et al. Among authors: zolkova j. Int J Mol Sci. 2020 Jun 29;21(13):4616. doi: 10.3390/ijms21134616. Int J Mol Sci. 2020. PMID: 32610551 Free PMC article. Review.
Impact of Edoxaban on Thrombin-Dependent Platelet Aggregation.
Sokol J, Nehaj F, Ivankova J, Mokan M, Lisa L, Zolkova J, Vadelova L, Mokan M, Stasko J. Sokol J, et al. Among authors: zolkova j. Clin Appl Thromb Hemost. 2020 Jan-Dec;26:1076029620948585. doi: 10.1177/1076029620948585. Clin Appl Thromb Hemost. 2020. PMID: 33054412 Free PMC article.
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, Ceznerova E, Kolkova Z, Loderer D, Neerman-Arbez M, Casini A, Brunclikova M, Skornova I, Dobrotova M, Grendar M, Stasko J, Kubisz P. Simurda T, et al. Among authors: zolkova j. Biomedicines. 2020 Dec 13;8(12):605. doi: 10.3390/biomedicines8120605. Biomedicines. 2020. PMID: 33322159 Free PMC article.
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