Komáromi I - Search Results

1

Molecular characterization of p.Asp77Gly and the novel p.Ala163Val and p.Ala163Glu mutations causing protein C deficiency.

Kovács KB, Pataki I, Bárdos H, Fekete A, Pfliegler G, Haramura G, Gindele R, Komáromi I, Balla G, Ádány R, Muszbek L, Bereczky Z. Kovács KB, et al. Among authors: komaromi i. Thromb Res. 2015 Apr;135(4):718-26. doi: 10.1016/j.thromres.2015.01.011. Epub 2015 Jan 15. Thromb Res. 2015. PMID: 25618265

2

Val34Leu polymorphism of plasma factor XIII: biochemistry and epidemiology in familial thrombophilia.

Balogh I, Szôke G, Kárpáti L, Wartiovaara U, Katona E, Komáromi I, Haramura G, Pfliegler G, Mikkola H, Muszbek L. Balogh I, et al. Among authors: komaromi i. Blood. 2000 Oct 1;96(7):2479-86. Blood. 2000. PMID: 11001900 Free article.

3

Phenotype-genotype characterization of 10 families with severe a subunit factor XIII deficiency.

Peyvandi F, Tagliabue L, Menegatti M, Karimi M, Komáromi I, Katona E, Muszbek L, Mannucci PM. Peyvandi F, et al. Among authors: komaromi i. Hum Mutat. 2004 Jan;23(1):98. doi: 10.1002/humu.9206. Hum Mutat. 2004. PMID: 14695539

4

Factor XDebrecen: Gly204Arg mutation in factor X causes the synthesis of a non-secretable protein and severe factor X deficiency.

Bereczky Z, Bárdos H, Komáromi I, Kiss C, Haramura G, Ajzner E, Adány R, Muszbek L. Bereczky Z, et al. Among authors: komaromi i. Haematologica. 2008 Feb;93(2):299-302. doi: 10.3324/haematol.11746. Haematologica. 2008. PMID: 18245654 Free article.

5

Cleavage of factor XIII by human neutrophil elastase results in a novel active truncated form of factor XIII A subunit.

Bagoly Z, Fazakas F, Komáromi I, Haramura G, Tóth E, Muszbek L. Bagoly Z, et al. Among authors: komaromi i. Thromb Haemost. 2008 Apr;99(4):668-74. doi: 10.1160/TH07-09-0577. Thromb Haemost. 2008. PMID: 18392324

6

Inherited factor V deficiency associated with a novel heterozygous missense mutation (p.G493R) in a patient with excessive surgical bleeding.

Kovács KB, Tisza B, Komáromi I, Muszbek L, Bereczky Z. Kovács KB, et al. Among authors: komaromi i. Thromb Haemost. 2009 Oct;102(4):787-9. doi: 10.1160/TH-09-04-0272. Thromb Haemost. 2009. PMID: 19806267 No abstract available.

7

Factor XIII: novel structural and functional aspects.

Komáromi I, Bagoly Z, Muszbek L. Komáromi I, et al. J Thromb Haemost. 2011 Jan;9(1):9-20. doi: 10.1111/j.1538-7836.2010.04070.x. J Thromb Haemost. 2011. PMID: 20880254 Free article. Review.

8

Antithrombin deficiency and its laboratory diagnosis.

Muszbek L, Bereczky Z, Kovács B, Komáromi I. Muszbek L, et al. Among authors: komaromi i. Clin Chem Lab Med. 2010 Dec;48 Suppl 1:S67-78. doi: 10.1515/CCLM.2010.368. Epub 2010 Nov 10. Clin Chem Lab Med. 2010. PMID: 21062218 Review.

9

Factor XIII: a coagulation factor with multiple plasmatic and cellular functions.

Muszbek L, Bereczky Z, Bagoly Z, Komáromi I, Katona É. Muszbek L, et al. Among authors: komaromi i. Physiol Rev. 2011 Jul;91(3):931-72. doi: 10.1152/physrev.00016.2010. Physiol Rev. 2011. PMID: 21742792 Free article. Review.

10

Three novel germ-line VHL mutations in Hungarian von Hippel-Lindau patients, including a nonsense mutation in a fifteen-year-old boy with renal cell carcinoma.

Losonczy G, Fazakas F, Pfliegler G, Komáromi I, Balázs E, Pénzes K, Berta A. Losonczy G, et al. Among authors: komaromi i. BMC Med Genet. 2013 Jan 8;14:3. doi: 10.1186/1471-2350-14-3. BMC Med Genet. 2013. PMID: 23298237 Free PMC article.

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