Schwaab R - Search Results

1

Congenital deficiency of vitamin K dependent coagulation factors in two families presents as a genetic defect of the vitamin K-epoxide-reductase-complex.

Oldenburg J, von Brederlow B, Fregin A, Rost S, Wolz W, Eberl W, Eber S, Lenz E, Schwaab R, Brackmann HH, Effenberger W, Harbrecht U, Schurgers LJ, Vermeer C, Müller CR. Oldenburg J, et al. Among authors: schwaab r. Thromb Haemost. 2000 Dec;84(6):937-41. Thromb Haemost. 2000. PMID: 11154138

2

Molecular biology of blood coagulation.

Oldenburg J, Schwaab R. Oldenburg J, et al. Among authors: schwaab r. Semin Thromb Hemost. 2001 Aug;27(4):313-24. doi: 10.1055/s-2001-16885. Semin Thromb Hemost. 2001. PMID: 11547354 Review.

3

HLA genotype of patients with severe haemophilia A due to intron 22 inversion with and without inhibitors of factor VIII.

Oldenburg J, Picard JK, Schwaab R, Brackmann HH, Tuddenham EG, Simpson E. Oldenburg J, et al. Among authors: schwaab r. Thromb Haemost. 1997 Feb;77(2):238-42. Thromb Haemost. 1997. PMID: 9157573

4

Missense mutations at ALA-10 in the factor IX propeptide: an insignificant variant in normal life but a decisive cause of bleeding during oral anticoagulant therapy.

Oldenburg J, Quenzel EM, Harbrecht U, Fregin A, Kress W, Müller CR, Hertfelder HJ, Schwaab R, Brackmann HH, Hanfland P. Oldenburg J, et al. Among authors: schwaab r. Br J Haematol. 1997 Jul;98(1):240-4. doi: 10.1046/j.1365-2141.1997.2213036.x. Br J Haematol. 1997. PMID: 9233593 Free article.

5

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: schwaab r. 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.

6

Haemophilia A diagnosis by automated fluorescent DNA detection of ten factor VIII intron 13 dinucleotide repeat alleles.

Kochhan L, Lalloz MR, Oldenburg J, McVey JH, Olek K, Brackmann HH, Tuddenham EG, Schwaab R. Kochhan L, et al. Among authors: schwaab r. Blood Coagul Fibrinolysis. 1994 Aug;5(4):497-501. Blood Coagul Fibrinolysis. 1994. PMID: 7841304

7

Two years' experience with two recombinant factor VIII concentrates.

Brackmann HH, Aygören E, Scharrer I, Schwaab R, Hammerstein U, Oldenburg J. Brackmann HH, et al. Among authors: schwaab r. Blood Coagul Fibrinolysis. 1993 Jun;4(3):421-4. doi: 10.1097/00001721-199306000-00004. Blood Coagul Fibrinolysis. 1993. PMID: 8329567

8

Haemophilia A: mutation type determines risk of inhibitor formation.

Schwaab R, Brackmann HH, Meyer C, Seehafer J, Kirchgesser M, Haack A, Olek K, Tuddenham EG, Oldenburg J. Schwaab R, et al. Thromb Haemost. 1995 Dec;74(6):1402-6. Thromb Haemost. 1995. PMID: 8772209

9

Mutations in severe hemophilia A: distribution within the factor VIII gene, origin and influence on inhibitor development.

Oldenburg J, Grimm T, Becker J, Olek K, Brackmann HH, Schwaab R. Oldenburg J, et al. Among authors: schwaab r. Beitr Infusionsther Transfusionsmed. 1997;34:224-30. Beitr Infusionsther Transfusionsmed. 1997. PMID: 9356677 No abstract available.

10

Small deletion/insertion mutations within poly-A runs of the factor VIII gene mitigate the severe haemophilia A phenotype.

Oldenburg J, Schröder J, Schmitt C, Brackmann HH, Schwaab R. Oldenburg J, et al. Among authors: schwaab r. Thromb Haemost. 1998 Feb;79(2):452-3. Thromb Haemost. 1998. PMID: 9493612 No abstract available.

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