Oldenburg J - Search Results

1

11 hemophilia A patients without mutations in the factor VIII encoding gene.

Klopp N, Oldenburg J, Uen C, Schneppenheim R, Graw J. Klopp N, et al. Among authors: oldenburg j. Thromb Haemost. 2002 Aug;88(2):357-60. Thromb Haemost. 2002. PMID: 12195713 No abstract available.

2

Analysis of mRNA in hemophilia A patients with undetectable mutations reveals normal splicing in the factor VIII gene.

El-Maarri O, Herbiniaux U, Graw J, Schröder J, Terzic A, Watzka M, Brackmann HH, Schramm W, Hanfland P, Schwaab R, Müller CR, Oldenburg J. El-Maarri O, et al. Among authors: oldenburg j. J Thromb Haemost. 2005 Feb;3(2):332-9. doi: 10.1111/j.1538-7836.2005.01140.x. J Thromb Haemost. 2005. PMID: 15670040 Free article.

3

[2% Haemophilia A patients without mutation in the FVIII gene].

Uen C, Oldenburg J, Schröder J, Brackmann HJ, Schramm W, Schwaab R, Schneppenheim R, Graw J. Uen C, et al. Among authors: oldenburg j. Hamostaseologie. 2003 Feb;23(1):1-5. Hamostaseologie. 2003. PMID: 12567191 German.

4

Results of a screening for von Willebrand disease type 2N in patients with suspected haemophilia A or von Willebrand disease type 1.

Schneppenheim R, Budde U, Krey S, Drewke E, Bergmann F, Lechler E, Oldenburg J, Schwaab R. Schneppenheim R, et al. Among authors: oldenburg j. Thromb Haemost. 1996 Oct;76(4):598-602. Thromb Haemost. 1996. PMID: 8903002 Clinical Trial.

5

Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2N.

Berber E, Fidanci ID, Un C, El-Maarri O, Aktuglu G, Gurgey A, Celkan T, Meral A, Oldenburg J, Graw J, Akar N, Caglayan H. Berber E, et al. Among authors: oldenburg j. Haemophilia. 2006 Jul;12(4):398-400. doi: 10.1111/j.1365-2516.2006.01302.x. Haemophilia. 2006. PMID: 16834740

6

[Characterization of factor VIII antibody epitopes from haemophilia A patients using cellulose bound FVIII peptide libraries].

Albert T, Lange S, Oldenburg J, Graw J, Schramm W, Hanfland P, Brackmann HH, Schwaab R. Albert T, et al. Among authors: oldenburg j. Hamostaseologie. 2003 Feb;23(1):13-7. Hamostaseologie. 2003. PMID: 12567194 German.

7

A common 253-kb deletion involving VWF and TMEM16B in German and Italian patients with severe von Willebrand disease type 3.

Schneppenheim R, Castaman G, Federici AB, Kreuz W, Marschalek R, Oldenburg J, Oyen F, Budde U. Schneppenheim R, et al. Among authors: oldenburg j. J Thromb Haemost. 2007 Apr;5(4):722-8. doi: 10.1111/j.1538-7836.2007.02460.x. Epub 2007 Feb 26. J Thromb Haemost. 2007. PMID: 17371490 Free article.

8

[Gathering and evaluation of phenotype data of haemophilia A patients for correlation with genotype data].

Brackmann HH, Albert T, Graw J, Oldenburg J, Schramm W, Schwaab R. Brackmann HH, et al. Among authors: oldenburg j. Hamostaseologie. 2003 Feb;23(1):24-7. Hamostaseologie. 2003. PMID: 12567196 German.

9

The problem of novel FVIII missense mutations for haemophilia A genetic counseling.

Schneppenheim R, Schröder J, Obser T, Oyen F, Schneppenheim S, Oldenburg J. Schneppenheim R, et al. Among authors: oldenburg j. Hamostaseologie. 2009 May;29(2):158-60. Hamostaseologie. 2009. PMID: 19404520

10

[Significance of mutation analysis in patients with haemophilia A].

Oldenburg J, Schröder J, Graw J, Ivaskevicius V, Brackmann HH, Schramm W, Müller CR, Seifried E, Schwaab R. Oldenburg J, et al. Hamostaseologie. 2003 Feb;23(1):6-12. Hamostaseologie. 2003. PMID: 12567193 German.

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