Ivaškevičius V - Search Results

1

Combined coagulation factor VIII and factor IX deficiency (CDF8F9) in a patient from Lithuania.

Ivaškevičius V, Pezeshkpoor B, Biswas A, Goldmann G, Horneff S, Gimbutyte M, Malciute L, Jurgutis R, Oldenburg J. Ivaškevičius V, et al. Hamostaseologie. 2016 Nov 8;36(Suppl. 2):S29-S33. Hamostaseologie. 2016. PMID: 27824213

2

Eight novel F13A1 gene missense mutations in patients with mild FXIII deficiency: in silico analysis suggests changes in FXIII-A subunit structure/function.

Biswas A, Ivaskevicius V, Thomas A, Varvenne M, Brand B, Rott H, Haussels I, Ruehl H, Scholz U, Klamroth R, Oldenburg J. Biswas A, et al. Among authors: ivaskevicius v. Ann Hematol. 2014 Oct;93(10):1665-76. doi: 10.1007/s00277-014-2102-4. Epub 2014 Jun 3. Ann Hematol. 2014. PMID: 24889649

3

The first case of combined coagulation factor V and coagulation factor VIII deficiency in Poland due to a novel p.Tyr135Asn missense mutation in the MCFD2 gene.

Ivaskevicius V, Windyga J, Baran B, Bykowska K, Daugela L, Watzka M, Seifried E, Oldenburg J. Ivaskevicius V, et al. Blood Coagul Fibrinolysis. 2008 Sep;19(6):531-534. doi: 10.1097/MBC.0b013e3283061103. Blood Coagul Fibrinolysis. 2008. PMID: 18685427

4

International registry on factor XIII deficiency: a basis formed mostly on European data.

Ivaskevicius V, Seitz R, Kohler HP, Schroeder V, Muszbek L, Ariens RA, Seifried E, Oldenburg J; Study Group. Ivaskevicius V, et al. Thromb Haemost. 2007 Jun;97(6):914-21. Thromb Haemost. 2007. PMID: 17549292

5

Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function.

Ivaskevicius V, Biswas A, Bevans C, Schroeder V, Kohler HP, Rott H, Halimeh S, Petrides PE, Lenk H, Krause M, Miterski B, Harbrecht U, Oldenburg J. Ivaskevicius V, et al. Haematologica. 2010 Jun;95(6):956-62. doi: 10.3324/haematol.2009.017210. Epub 2010 Feb 23. Haematologica. 2010. PMID: 20179087 Free PMC article.

6

Insights into pathological mechanisms of missense mutations in C-terminal domains of von Willebrand factor causing qualitative or quantitative von Willebrand disease.

Yadegari H, Driesen J, Pavlova A, Biswas A, Ivaskevicius V, Klamroth R, Oldenburg J. Yadegari H, et al. Among authors: ivaskevicius v. Haematologica. 2013 Aug;98(8):1315-23. doi: 10.3324/haematol.2013.084111. Epub 2013 Mar 28. Haematologica. 2013. PMID: 23539537 Free PMC article.

7

Intron retention resulting from a silent mutation in the VWF gene that structurally influences the 5' splice site.

Yadegari H, Biswas A, Akhter MS, Driesen J, Ivaskevicius V, Marquardt N, Oldenburg J. Yadegari H, et al. Among authors: ivaskevicius v. Blood. 2016 Oct 27;128(17):2144-2152. doi: 10.1182/blood-2016-02-699686. Epub 2016 Aug 19. Blood. 2016. PMID: 27543438 Free PMC article.

8

Recurrent VTE in a heterozygote of the fibrinogen Aα IVS4+1G>T and Aα p.Arg168Ter mutation.

Berens C, Rühl H, Ivaškevičius V, Oldenburg J, Hertfelder HJ, Pötzsch B. Berens C, et al. Among authors: ivaskevicius v. Thromb Haemost. 2016 May 2;115(5):1073-5. doi: 10.1160/TH15-10-0818. Epub 2016 Jan 14. Thromb Haemost. 2016. PMID: 26763372 No abstract available.

9

Structural and functional influences of coagulation factor XIII subunit B heterozygous missense mutants.

Thomas A, Biswas A, Ivaskevicius V, Oldenburg J. Thomas A, et al. Among authors: ivaskevicius v. Mol Genet Genomic Med. 2015 Jul;3(4):258-71. doi: 10.1002/mgg3.138. Epub 2015 Apr 10. Mol Genet Genomic Med. 2015. PMID: 26247044 Free PMC article.

10

In vitro secretion deficits are common among human coagulation factor XIII subunit B missense mutants: correlations with patient phenotypes and molecular models.

Biswas A, Thomas A, Bevans CG, Ivaskevicius V, Oldenburg J. Biswas A, et al. Among authors: ivaskevicius v. Hum Mutat. 2013 Nov;34(11):1490-500. doi: 10.1002/humu.22391. Epub 2013 Sep 13. Hum Mutat. 2013. PMID: 23913518

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