Brackmann HH - Search Results

1

Inhibitors in German hemophilia A patients treated with a double virus inactivated factor VIII concentrate bind to the C2 domain of FVIII light chain.

Laub R, Di Giambattista M, Fondu P, Brackmann HH, Lenk H, Saenko EL, Felch M, Scandella D. Laub R, et al. Among authors: brackmann hh. Thromb Haemost. 1999 Jan;81(1):39-44. Thromb Haemost. 1999. PMID: 9974372

2

German recommendations for immune tolerance therapy in type A haemophiliacs with antibodies.

Brackmann HH, Lenk H, Scharrer I, Auerswald G, Kreuz W. Brackmann HH, et al. Haemophilia. 1999 May;5(3):203-6. doi: 10.1046/j.1365-2516.1999.00311.x. Haemophilia. 1999. PMID: 10444288

3

Pharmacokinetics and tolerability of factor XIII concentrates prepared from human placenta or plasma: a crossover randomised study.

Brackmann HH, Egbring R, Ferster A, Fondu P, Girardel JM, Kreuz W, Masure R, Miloszewski K, Stibbe J, Zimmermann R, et al. Brackmann HH, et al. Thromb Haemost. 1995 Aug;74(2):622-5. Thromb Haemost. 1995. PMID: 8584996 Clinical Trial.

4

Sucrose formulated recombinant human antihemophilic factor VIII is safe and efficacious for treatment of hemophilia A in home therapy--International Kogenate-FS Study Group.

Abshire TC, Brackmann HH, Scharrer I, Hoots K, Gazengel C, Powell JS, Gorina E, Kellermann E, Vosburgh E. Abshire TC, et al. Among authors: brackmann hh. Thromb Haemost. 2000 Jun;83(6):811-6. Thromb Haemost. 2000. PMID: 10896230 Clinical Trial.

5

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: brackmann hh. Thromb Haemost. 1997 Feb;77(2):238-42. Thromb Haemost. 1997. PMID: 9157573

6

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. Among authors: brackmann hh. Thromb Haemost. 1995 Dec;74(6):1402-6. Thromb Haemost. 1995. PMID: 8772209

7

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: brackmann hh. Thromb Haemost. 1998 Feb;79(2):452-3. Thromb Haemost. 1998. PMID: 9493612 No abstract available.

8

Beta-propiolactone UV inactivated clotting factor concentrate is the source of HIV-infection of 8 hemophilia B patients: confirmed.

Kupfer B, Oldenburg J, Brackmann HH, Matz B, Schneweis KE, Kaiser R. Kupfer B, et al. Among authors: brackmann hh. Thromb Haemost. 1995 Nov;74(5):1386-7. Thromb Haemost. 1995. PMID: 8607133 No abstract available.

9

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: brackmann hh. 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.

10

A novel cause of mild/moderate hemophilia A: mutations scattered in the factor VIII C1 domain reduce factor VIII binding to von Willebrand factor.

Jacquemin M, Lavend'homme R, Benhida A, Vanzieleghem B, d'Oiron R, Lavergne JM, Brackmann HH, Schwaab R, VandenDriessche T, Chuah MK, Hoylaerts M, Gilles JG, Peerlinck K, Vermylen J, Saint-Remy JM. Jacquemin M, et al. Among authors: brackmann hh. Blood. 2000 Aug 1;96(3):958-65. Blood. 2000. PMID: 10910910 Free article.

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