Ettingshausen CE - Search Results

1

Effects of the factor V G1691A mutation and the factor II G20210A variant on the clinical expression of severe hemophilia A in children--results of a multicenter studys.

Kurnik K, Kreuz W, Horneff S, Düring C, Schobess R, Bidlingmaier C, Ettingshausen CE, Krümpel A, Bogdanova N, Nowak-Göttl U. Kurnik K, et al. Among authors: ettingshausen ce. Haematologica. 2007 Jul;92(7):982-5. doi: 10.3324/haematol.11161. Haematologica. 2007. PMID: 17606451 Free article.

2

Replacement therapy with protein C concentrate in infants and adolescents with meningococcal sepsis and purpura fulminans.

Ettingshausen CE, Veldmann A, Beeg T, Schneider W, Jäger G, Kreuz W. Ettingshausen CE, et al. Semin Thromb Hemost. 1999;25(6):537-41. doi: 10.1055/s-2007-994962. Semin Thromb Hemost. 1999. PMID: 10632475 Clinical Trial.

3

Portal vein thrombosis in a patient with severe haemophilia A and F V G1691A mutation during continuous infusion of F VIII after intramural jejunal bleeding--successful thrombolysis under heparin therapy.

Ettingshausen CE, Saguer IM, Kreuz W. Ettingshausen CE, et al. Eur J Pediatr. 1999 Dec;158 Suppl 3:S180-2. doi: 10.1007/pl00014351. Eur J Pediatr. 1999. PMID: 10650865

4

Catheter-related thrombosis in children with hemophilia A: evidence of a multifactorial disease.

Ettingshausen CE, Kurnik K, Schobess R, Kreuz WD, Halimeh S, Pollman H, Nowak-Göttl U. Ettingshausen CE, et al. Blood. 2002 Feb 15;99(4):1499-500. doi: 10.1182/blood.v99.4.1499. Blood. 2002. PMID: 11852883 Free article. No abstract available.

5

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: ettingshausen ce. Semin Thromb Hemost. 2002 Jun;28(3):285-90. doi: 10.1055/s-2002-32664. Semin Thromb Hemost. 2002. PMID: 12098090

6

Epidemiology of inhibitors and current treatment strategies.

Kreuz W, Ettingshausen CE, Auerswald G, Saguer IM, Becker S, Funk M, Heller C, Klarmann D, Klingebiel T; GTH PUP Study Group. Kreuz W, et al. Among authors: ettingshausen ce. Haematologica. 2003 Jun;88(6):EREP04. Haematologica. 2003. PMID: 12826530 Review.

7

Long-term aspects of hemophilia B treatment: part I-role for prophylaxis.

Ettingshausen CE, Kreuz W. Ettingshausen CE, et al. Blood Coagul Fibrinolysis. 2004 Jun;15 Suppl 2:S11-3. doi: 10.1097/00001721-200406002-00004. Blood Coagul Fibrinolysis. 2004. PMID: 15322452 Review.

8

Role of von Willebrand factor in immune tolerance induction.

Ettingshausen CE, Kreuz W. Ettingshausen CE, et al. Blood Coagul Fibrinolysis. 2005 Apr;16 Suppl 1:S27-31. doi: 10.1097/01.mbc.0000167660.30886.e9. Blood Coagul Fibrinolysis. 2005. PMID: 15849524 Review.

9

Recombinant vs. plasma-derived products, especially those with intact VWF, regarding inhibitor development.

Ettingshausen CE, Kreuz W. Ettingshausen CE, et al. Haemophilia. 2006 Dec;12 Suppl 6:102-6. doi: 10.1111/j.1365-2516.2006.01373.x. Haemophilia. 2006. PMID: 17123402 Review.

10

Early long-term FEIBA prophylaxis in haemophilia A patients with inhibitor after failing immune tolerance induction: A prospective clinical case series.

Ettingshausen CE, Kreuz W. Ettingshausen CE, et al. Haemophilia. 2010 Jan;16(1):90-100. doi: 10.1111/j.1365-2516.2009.02116.x. Epub 2009 Oct 29. Haemophilia. 2010. PMID: 19878335

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