Oyen F - Search Results

1

Germline variants in SMARCB1 and other members of the BAF chromatin-remodeling complex across human disease entities: a meta-analysis.

Holsten T, Bens S, Oyen F, Nemes K, Hasselblatt M, Kordes U, Siebert R, Frühwald MC, Schneppenheim R, Schüller U. Holsten T, et al. Among authors: oyen f. Eur J Hum Genet. 2018 Aug;26(8):1083-1093. doi: 10.1038/s41431-018-0143-1. Epub 2018 Apr 30. Eur J Hum Genet. 2018. PMID: 29706634 Free PMC article. Review.

2

von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP.

Schneppenheim R, Budde U, Oyen F, Angerhaus D, Aumann V, Drewke E, Hassenpflug W, Häberle J, Kentouche K, Kohne E, Kurnik K, Mueller-Wiefel D, Obser T, Santer R, Sykora KW. Schneppenheim R, et al. Among authors: oyen f. Blood. 2003 Mar 1;101(5):1845-50. doi: 10.1182/blood-2002-08-2399. Epub 2002 Oct 17. Blood. 2003. PMID: 12393505 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: oyen f. Thromb Haemost. 2004 Jul;92(1):36-41. doi: 10.1160/TH04-02-0084. Thromb Haemost. 2004. PMID: 15213842

4

A common origin of the 4143insA ADAMTS13 mutation.

Schneppenheim R, Kremer Hovinga JA, Becker T, Budde U, Karpman D, Brockhaus W, Hrachovinová I, Korczowski B, Oyen F, Rittich S, von Rosen J, Tjønnfjord GE, Pimanda JE, Wienker TF, Lämmle B. Schneppenheim R, et al. Among authors: oyen f. Thromb Haemost. 2006 Jul;96(1):3-6. doi: 10.1160/TH05-12-0817. Thromb Haemost. 2006. PMID: 16807643

5

Intracranial hemorrhage in a term newborn with severe von Willebrand disease type 3 associated with sinus venous thrombosis.

Wetzstein V, Budde U, Oyen F, Ding X, Herrmann J, Liebig B, Schneppenheim R. Wetzstein V, et al. Among authors: oyen f. Haematologica. 2006 Dec;91(12 Suppl):ECR60. Haematologica. 2006. PMID: 17194666

6

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: oyen f. 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.

7

Analysis of the CC chemokine receptor 5Delta32 polymorphism in pediatric liver transplant recipients.

Fischer-Maas L, Schneppenheim R, Oyen F, Grabhorn E, Richter A, Fischer L, Ganschow R. Fischer-Maas L, et al. Among authors: oyen f. Pediatr Transplant. 2008 Nov;12(7):769-72. doi: 10.1111/j.1399-3046.2007.00900.x. Epub 2008 Jan 8. Pediatr Transplant. 2008. PMID: 18194353

8

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: oyen f. Hamostaseologie. 2009 May;29(2):158-60. Hamostaseologie. 2009. PMID: 19404520

9

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: oyen f. Hamostaseologie. 2009 May;29(2):143-8. Hamostaseologie. 2009. PMID: 19404524

10

Recurrent loss, but lack of mutations, of the SMARCB1 tumor suppressor gene in T-cell prolymphocytic leukemia with TCL1A-TCRAD juxtaposition.

Bug S, Dürig J, Oyen F, Klein-Hitpass L, Martin-Subero JI, Harder L, Baudis M, Arnold N, Kordes U, Dührsen U, Schneppenheim R, Siebert R. Bug S, et al. Among authors: oyen f. Cancer Genet Cytogenet. 2009 Jul;192(1):44-7. doi: 10.1016/j.cancergencyto.2009.03.001. Cancer Genet Cytogenet. 2009. PMID: 19480937

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