Oldenburg J - Search Results

1

Risk Factors for the Progression from Low to High Titres in 260 Children with Severe Haemophilia A and Newly Developed Inhibitors.

Mancuso ME, Fischer K, Santagostino E, Oldenburg J, Platokouki H, Königs C, Escuriola-Ettingshausen C, Rivard GE, Cid AR, Carcao M, Ljung R, Petrini P, Altisent C, Kenet G, Liesner R, Kurnik K, Auerswald G, Chambost H, Mäkipernaa A, Molinari AC, Williams M, van den Berg HM; European Pediatric Network for Haemophilia Management (PedNet) the REMAIN (REal life MAnagement of children with INhibitors) Study Group. Mancuso ME, et al. Among authors: oldenburg j. Thromb Haemost. 2017 Dec;117(12):2274-2282. doi: 10.1160/TH17-01-0059. Epub 2017 Dec 6. Thromb Haemost. 2017. PMID: 29212115

2

Inhibitor development in previously untreated patients with hemophilia A: a prospective long-term follow-up comparing plasma-derived and recombinant products.

Kreuz W, Ettingshausen CE, Zyschka A, Oldenburg J, Saguer IM, Ehrenforth S, Klingebiel T. Kreuz W, et al. Among authors: oldenburg j. Semin Thromb Hemost. 2002 Jun;28(3):285-90. doi: 10.1055/s-2002-32664. Semin Thromb Hemost. 2002. PMID: 12098090

3

Recombinant expression of mutations causing von Willebrand disease type Normandy: characterization of a combined defect of factor VIII binding and multimerization.

Schneppenheim R, Lenk H, Obser T, Oldenburg J, Oyen F, Schneppenheim S, Schwaab R, Will K, Budde U. Schneppenheim R, et al. Among authors: oldenburg j. Thromb Haemost. 2004 Jul;92(1):36-41. doi: 10.1160/TH04-02-0084. Thromb Haemost. 2004. PMID: 15213842

4

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. Thromb Haemost. 2006 May;95(5):903-5. Thromb Haemost. 2006. PMID: 16676088 No abstract available.

5

Characterisation of two novel large F8 deletions in patients with severe haemophilia A and factor VIII inhibitors.

Roth L, Marschalek R, Oldenburg J, Oyen F, Schneppenheim R. Roth L, et al. Among authors: oldenburg j. Thromb Haemost. 2011 Feb;105(2):279-84. doi: 10.1160/TH10-09-0570. Epub 2010 Nov 23. Thromb Haemost. 2011. PMID: 21103668

6

Report of the Fifth meeting of the International Network for Pediatric Hemophilia: a focus on prophylaxis and immune tolerance induction.

Ljung R, Oldenburg J, Auerswald G, van den Berg M, Shima M, DiMichele D. Ljung R, et al. Among authors: oldenburg j. Int J Hematol. 2011 Oct;94(4):415-421. doi: 10.1007/s12185-011-0925-5. Epub 2011 Sep 28. Int J Hematol. 2011. PMID: 21953272 No abstract available.

7

Thrombin inhibition profiles in healthy individuals and thrombophilic patients.

Rühl H, Müller J, Harbrecht U, Fimmers R, Oldenburg J, Mayer G, Pötzsch B. Rühl H, et al. Among authors: oldenburg j. Thromb Haemost. 2012 May;107(5):848-53. doi: 10.1160/TH11-10-0719. Epub 2012 Jan 25. Thromb Haemost. 2012. PMID: 22274722

8

F8 gene mutation type and inhibitor development in patients with severe hemophilia A: systematic review and meta-analysis.

Gouw SC, van den Berg HM, Oldenburg J, Astermark J, de Groot PG, Margaglione M, Thompson AR, van Heerde W, Boekhorst J, Miller CH, le Cessie S, van der Bom JG. Gouw SC, et al. Among authors: oldenburg j. Blood. 2012 Mar 22;119(12):2922-34. doi: 10.1182/blood-2011-09-379453. Epub 2012 Jan 26. Blood. 2012. PMID: 22282501 Free article. Review.

9

Recombinant factor XIII: a safe and novel treatment for congenital factor XIII deficiency.

Inbal A, Oldenburg J, Carcao M, Rosholm A, Tehranchi R, Nugent D. Inbal A, et al. Among authors: oldenburg j. Blood. 2012 May 31;119(22):5111-7. doi: 10.1182/blood-2011-10-386045. Epub 2012 Mar 26. Blood. 2012. PMID: 22451421 Free article. Clinical Trial.

10

Mutation distribution in the von Willebrand factor gene related to the different von Willebrand disease (VWD) types in a cohort of VWD patients.

Yadegari H, Driesen J, Pavlova A, Biswas A, Hertfelder HJ, Oldenburg J. Yadegari H, et al. Among authors: oldenburg j. Thromb Haemost. 2012 Oct;108(4):662-71. doi: 10.1160/TH12-02-0089. Epub 2012 Aug 7. Thromb Haemost. 2012. PMID: 22871923

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