Schneppenheim S - Search Results

1

Impact of mutations in the von Willebrand factor A2 domain on ADAMTS13-dependent proteolysis.

Hassenpflug WA, Budde U, Obser T, Angerhaus D, Drewke E, Schneppenheim S, Schneppenheim R. Hassenpflug WA, et al. Among authors: schneppenheim s, schneppenheim r. Blood. 2006 Mar 15;107(6):2339-45. doi: 10.1182/blood-2005-04-1758. Epub 2005 Dec 1. Blood. 2006. PMID: 16322474 Free article.

2

Expression and characterization of von Willebrand factor dimerization defects in different types of von Willebrand disease.

Schneppenheim R, Budde U, Obser T, Brassard J, Mainusch K, Ruggeri ZM, Schneppenheim S, Schwaab R, Oldenburg J. Schneppenheim R, et al. Among authors: schneppenheim s. Blood. 2001 Apr 1;97(7):2059-66. doi: 10.1182/blood.v97.7.2059. Blood. 2001. PMID: 11264172 Free article.

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: schneppenheim s. Thromb Haemost. 2004 Jul;92(1):36-41. doi: 10.1160/TH04-02-0084. Thromb Haemost. 2004. PMID: 15213842

4

The spectrum of aldolase B (ALDOB) mutations and the prevalence of hereditary fructose intolerance in Central Europe.

Santer R, Rischewski J, von Weihe M, Niederhaus M, Schneppenheim S, Baerlocher K, Kohlschütter A, Muntau A, Posselt HG, Steinmann B, Schneppenheim R. Santer R, et al. Among authors: schneppenheim s, schneppenheim r. Hum Mutat. 2005 Jun;25(6):594. doi: 10.1002/humu.9343. Hum Mutat. 2005. PMID: 15880727

5

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: schneppenheim s. Hamostaseologie. 2009 May;29(2):158-60. Hamostaseologie. 2009. PMID: 19404520

6

Response to DDAVP in children with von Willebrand disease type 2.

Schneppenheim R, Budde U, Beutel K, Hassenpflug WA, Hauch H, Obser T, Oyen F, Schneppenheim S, Schrum J. Schneppenheim R, et al. Among authors: schneppenheim s. Hamostaseologie. 2009 May;29(2):143-8. Hamostaseologie. 2009. PMID: 19404524

7

Shear-induced unfolding activates von Willebrand factor A2 domain for proteolysis.

Baldauf C, Schneppenheim R, Stacklies W, Obser T, Pieconka A, Schneppenheim S, Budde U, Zhou J, Gräter F. Baldauf C, et al. Among authors: schneppenheim s, schneppenheim r. J Thromb Haemost. 2009 Dec;7(12):2096-105. doi: 10.1111/j.1538-7836.2009.03640.x. Epub 2009 Oct 8. J Thromb Haemost. 2009. PMID: 19817991 Free article.

8

The mutation N528S in the von Willebrand factor (VWF) propeptide causes defective multimerization and storage of VWF.

Haberichter SL, Budde U, Obser T, Schneppenheim S, Wermes C, Schneppenheim R. Haberichter SL, et al. Among authors: schneppenheim s, schneppenheim r. Blood. 2010 Jun 3;115(22):4580-7. doi: 10.1182/blood-2009-09-244327. Epub 2010 Mar 24. Blood. 2010. PMID: 20335223 Free PMC article.

9

A cluster of mutations in the D3 domain of von Willebrand factor correlates with a distinct subgroup of von Willebrand disease: type 2A/IIE.

Schneppenheim R, Michiels JJ, Obser T, Oyen F, Pieconka A, Schneppenheim S, Will K, Zieger B, Budde U. Schneppenheim R, et al. Among authors: schneppenheim s. Blood. 2010 Jun 10;115(23):4894-901. doi: 10.1182/blood-2009-07-226324. Epub 2010 Mar 29. Blood. 2010. PMID: 20351307 Free article.

10

Acquired type 2A von Willebrand syndrome caused by aortic valve disease corrects during valve surgery.

Solomon C, Budde U, Schneppenheim S, Czaja E, Hagl C, Schoechl H, von Depka M, Rahe-Meyer N. Solomon C, et al. Among authors: schneppenheim s. Br J Anaesth. 2011 Apr;106(4):494-500. doi: 10.1093/bja/aeq413. Epub 2011 Jan 28. Br J Anaesth. 2011. PMID: 21278152 Free article.

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