Oldenburg J - 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. 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

2

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

3

Different inactivating mutations in the LU genes of three individuals with the Lutheran-null phenotype.

Karamatic Crew V, Mallinson G, Green C, Poole J, Uchikawa M, Tani Y, Geisen C, Oldenburg J, Daniels G. Karamatic Crew V, et al. Among authors: oldenburg j. Transfusion. 2007 Mar;47(3):492-8. doi: 10.1111/j.1537-2995.2006.01141.x. Transfusion. 2007. PMID: 17319831

4

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.

5

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

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: 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

7

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

8

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

9

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.

10

Compound heterozygous mutations in the gamma-glutamyl carboxylase gene cause combined deficiency of all vitamin K-dependent blood coagulation factors.

Rost S, Fregin A, Koch D, Compes M, Müller CR, Oldenburg J. Rost S, et al. Among authors: oldenburg j. Br J Haematol. 2004 Aug;126(4):546-9. doi: 10.1111/j.1365-2141.2004.05071.x. Br J Haematol. 2004. PMID: 15287948 Free article.

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