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2020 3
2021 3
2022 0
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Page 1
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: brunclikova m. 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.
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: brunclikova m. Diagnostics (Basel). 2021 Nov 19;11(11):2140. doi: 10.3390/diagnostics11112140. Diagnostics (Basel). 2021. PMID: 34829490 Free PMC article. Review.
Multimer Analysis of Von Willebrand Factor in Von Willebrand Disease with a Hydrasys Semi-Automatic Analyzer-Single-Center Experience.
Skornova I, Simurda T, Stasko J, Zolkova J, Sokol J, Holly P, Dobrotova M, Plamenova I, Hudecek J, Brunclikova M, Stryckova A, Kubisz P. Skornova I, et al. Among authors: brunclikova m. Diagnostics (Basel). 2021 Nov 20;11(11):2153. doi: 10.3390/diagnostics11112153. Diagnostics (Basel). 2021. PMID: 34829500 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: brunclikova m. Biomedicines. 2020 Dec 13;8(12):605. doi: 10.3390/biomedicines8120605. Biomedicines. 2020. PMID: 33322159 Free PMC article.