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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: caccia s. 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.
Hepatic fibrinogen storage disease: identification of two novel mutations (p.Asp316Asn, fibrinogen Pisa and p.Gly366Ser, fibrinogen Beograd) impacting on the fibrinogen γ-module.
Asselta R, Robusto M, Braidotti P, Peyvandi F, Nastasio S, D'Antiga L, Perisic VN, Maggiore G, Caccia S, Duga S. Asselta R, et al. Among authors: caccia s. J Thromb Haemost. 2015 Aug;13(8):1459-67. doi: 10.1111/jth.13021. Epub 2015 Jul 14. J Thromb Haemost. 2015. PMID: 26039544 Free article.
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: caccia s. 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.
The expanding spectrum of PRPS1-associated phenotypes: three novel mutations segregating with X-linked hearing loss and mild peripheral neuropathy.
Robusto M, Fang M, Asselta R, Castorina P, Previtali SC, Caccia S, Benzoni E, De Cristofaro R, Yu C, Cesarani A, Liu X, Li W, Primignani P, Ambrosetti U, Xu X, Duga S, Soldà G. Robusto M, et al. Among authors: caccia s. Eur J Hum Genet. 2015 Jun;23(6):766-73. doi: 10.1038/ejhg.2014.168. Epub 2014 Sep 3. Eur J Hum Genet. 2015. PMID: 25182139 Free PMC article.
Anti-C1-Inhibitor Autoantibody Detection by ELISA.
Suffritti C, Caccia S, Berra S, Parolin D, Cicardi M. Suffritti C, et al. Among authors: caccia s. Methods Mol Biol. 2021;2227:115-120. doi: 10.1007/978-1-0716-1016-9_11. Methods Mol Biol. 2021. PMID: 33847936
Antibodies to tissue-type plasminogen activator (t-PA) in patients with inflammatory bowel disease: high prevalence, interactions with functional domains of t-PA and possible implications in thrombosis.
Saibeni S, Ciscato C, Vecchi M, Boscolo Anzoletti M, Kaczmarek E, Caccia S, de Franchis R, Cugno M. Saibeni S, et al. Among authors: caccia s. J Thromb Haemost. 2006 Jul;4(7):1510-6. doi: 10.1111/j.1538-7836.2006.01970.x. J Thromb Haemost. 2006. PMID: 16839347 Free article.
The spectrum of factor XI deficiency in Italy.
Castaman G, Giacomelli SH, Caccia S, Riccardi F, Rossetti G, Dragani A, Giuffrida AC, Biasoli C, Duga S. Castaman G, et al. Among authors: caccia s. Haemophilia. 2014 Jan;20(1):106-13. doi: 10.1111/hae.12257. Epub 2013 Sep 24. Haemophilia. 2014. PMID: 24112640
279 results