Ivaskevicius V - Search Results

1

gammaAla82Gly represents a common fibrinogen gamma-chain variant in Caucasians.

Ivaskevicius V, Jusciute E, Steffens M, Geisen C, Hanfland P, Wienker TF, Seifried E, Oldenburg J. Ivaskevicius V, et al. Blood Coagul Fibrinolysis. 2005 Apr;16(3):205-8. doi: 10.1097/01.mbc.0000164430.98169.c6. Blood Coagul Fibrinolysis. 2005. PMID: 15795540

2

Elastin polymorphism haplotype and intracranial aneurysms are not associated in Central Europe.

Hofer A, Hermans M, Kubassek N, Sitzer M, Funke H, Stögbauer F, Ivaskevicius V, Oldenburg J, Burtscher J, Knopp U, Schoch B, Wanke I, Hübner F, Deinsberger W, Meyer B, Boecher-Schwarz H, Poewe W, Raabe A, Steinmetz H, Auburger G. Hofer A, et al. Among authors: ivaskevicius v. Stroke. 2003 May;34(5):1207-11. doi: 10.1161/01.STR.0000069013.83336.1C. Epub 2003 Apr 10. Stroke. 2003. PMID: 12690215

3

Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2.

Rost S, Fregin A, Ivaskevicius V, Conzelmann E, Hörtnagel K, Pelz HJ, Lappegard K, Seifried E, Scharrer I, Tuddenham EG, Müller CR, Strom TM, Oldenburg J. Rost S, et al. Among authors: ivaskevicius v. Nature. 2004 Feb 5;427(6974):537-41. doi: 10.1038/nature02214. Nature. 2004. PMID: 14765194

4

Identification of 32 novel mutations in the factor VIII gene in Indian patients with hemophilia A.

Ahmed RP, Ivaskevicius V, Kannan M, Seifried E, Oldenburg J, Saxena R. Ahmed RP, et al. Among authors: ivaskevicius v. Haematologica. 2005 Feb;90(2):283-4. Haematologica. 2005. PMID: 15710596

5

Genetic background and inhibitors in previously untreated or minimally treated young patients with severe haemophilia A treated with sucrose-formulated recombinant factor VIII.

Oldenburg J, Ivaskevicius V, Schröder J, Müller CR, Ganguly A. Oldenburg J, et al. Among authors: ivaskevicius v. Thromb Haemost. 2006 May;95(5):903-5. Thromb Haemost. 2006. PMID: 16676088 No abstract available.

6

Protection from type 1 diabetes by vitamin D receptor haplotypes.

Ramos-Lopez E, Jansen T, Ivaskevicius V, Kahles H, Klepzig C, Oldenburg J, Badenhoop K. Ramos-Lopez E, et al. Among authors: ivaskevicius v. Ann N Y Acad Sci. 2006 Oct;1079:327-34. doi: 10.1196/annals.1375.050. Ann N Y Acad Sci. 2006. PMID: 17130574

7

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

8

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

9

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.

10

An update of the mutation profile of Factor 13 A and B genes.

Biswas A, Ivaskevicius V, Seitz R, Thomas A, Oldenburg J. Biswas A, et al. Among authors: ivaskevicius v. Blood Rev. 2011 Sep;25(5):193-204. doi: 10.1016/j.blre.2011.03.001. Epub 2011 Jun 2. Blood Rev. 2011. PMID: 21640452 Review.

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