Oldenburg J - Search Results

1

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: oldenburg j. Haematologica. 2005 Feb;90(2):283-4. Haematologica. 2005. PMID: 15710596

2

First report of a FVII-deficient Indian patient carrying double heterozygous mutations in the FVII gene.

Ahmed RP, Biswas A, Kannan M, Bhattacharya M, Geisen C, Seifried E, Oldenburg J, Saxena R. Ahmed RP, et al. Among authors: oldenburg j. Thromb Res. 2005;115(6):535-6. doi: 10.1016/j.thromres.2004.11.004. Epub 2004 Nov 24. Thromb Res. 2005. PMID: 15792686 No abstract available.

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: oldenburg j. Nature. 2004 Feb 5;427(6974):537-41. doi: 10.1038/nature02214. Nature. 2004. PMID: 14765194

4

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. Among authors: oldenburg j. Blood Coagul Fibrinolysis. 2005 Apr;16(3):205-8. doi: 10.1097/01.mbc.0000164430.98169.c6. Blood Coagul Fibrinolysis. 2005. PMID: 15795540

5

The Malmö International Brother Study (MIBS). Genetic defects and inhibitor development in siblings with severe hemophilia A.

Astermark J, Oldenburg J, Escobar M, White GC 2nd, Berntorp E; Malmö International Brother Study study group. Astermark J, et al. Among authors: oldenburg j. Haematologica. 2005 Jul;90(7):924-31. Haematologica. 2005. PMID: 15996930

6

A rare case of unprovoked venous thromboembolism manifestation in a young patient with antithrombin Type IIB deficiency combined with inferior vena cava anomaly from Lithuania.

Saulytė-Trakymienė S, Adomaitienė I, Unkrig S, Oldenburg J, Ivaškevičius V. Saulytė-Trakymienė S, et al. Among authors: oldenburg j. Hamostaseologie. 2017;37(S 01):S26-S31. doi: 10.5482/HAMO-17-03-0012. Epub 2017 Dec 28. Hamostaseologie. 2017. PMID: 29582922 English.

7

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: oldenburg j. Stroke. 2003 May;34(5):1207-11. doi: 10.1161/01.STR.0000069013.83336.1C. Epub 2003 Apr 10. Stroke. 2003. PMID: 12690215

8

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: oldenburg j. Ann N Y Acad Sci. 2006 Oct;1079:327-34. doi: 10.1196/annals.1375.050. Ann N Y Acad Sci. 2006. PMID: 17130574

9

VKORC1 haplotypes and their impact on the inter-individual and inter-ethnical variability of oral anticoagulation.

Geisen C, Watzka M, Sittinger K, Steffens M, Daugela L, Seifried E, Müller CR, Wienker TF, Oldenburg J. Geisen C, et al. Among authors: oldenburg j. Thromb Haemost. 2005 Oct;94(4):773-9. doi: 10.1160/TH05-04-0290. Thromb Haemost. 2005. PMID: 16270629

10

Polymorphisms in the IL10 but not in the IL1beta and IL4 genes are associated with inhibitor development in patients with hemophilia A.

Astermark J, Oldenburg J, Pavlova A, Berntorp E, Lefvert AK; MIBS Study Group. Astermark J, et al. Among authors: oldenburg j. Blood. 2006 Apr 15;107(8):3167-72. doi: 10.1182/blood-2005-09-3918. Epub 2005 Dec 27. Blood. 2006. PMID: 16380445 Free article.

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