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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: asselta r. 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.
Molecular genetics of quantitative fibrinogen disorders.
Asselta R, Spena S, Duga S, Tenchini ML. Asselta R, et al. Cardiovasc Hematol Agents Med Chem. 2007 Apr;5(2):163-73. doi: 10.2174/187152507780363205. Cardiovasc Hematol Agents Med Chem. 2007. PMID: 17430139 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: asselta r. 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.
Hereditary Hypofibrinogenemia with Hepatic Storage.
Asselta R, Paraboschi EM, Duga S. Asselta R, et al. Int J Mol Sci. 2020 Oct 22;21(21):7830. doi: 10.3390/ijms21217830. Int J Mol Sci. 2020. PMID: 33105716 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: asselta r. Diagnostics (Basel). 2021 Nov 19;11(11):2140. doi: 10.3390/diagnostics11112140. Diagnostics (Basel). 2021. PMID: 34829490 Free PMC article. Review.
210 results