Hanfland P - Search Results

1

gammaAla82Gly represents a common fibrinogen gamma-chain variant in Caucasians.

Ivaskevicius V, Jusciute E, Steffens M, Geisen C, Hanfland P, Wienker TF, Seifried E, Oldenburg J. Ivaskevicius V, et al. Among authors: hanfland p. Blood Coagul Fibrinolysis. 2005 Apr;16(3):205-8. doi: 10.1097/01.mbc.0000164430.98169.c6. Blood Coagul Fibrinolysis. 2005. PMID: 15795540

2

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: hanfland p. 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.

3

Lack of F8 mRNA: a novel mechanism leading to hemophilia A.

El-Maarri O, Singer H, Klein C, Watzka M, Herbiniaux U, Brackmann HH, Schröder J, Graw J, Müller CR, Schramm W, Schwaab R, Haaf T, Hanfland P, Oldenburg J. El-Maarri O, et al. Among authors: hanfland p. Blood. 2006 Apr 1;107(7):2759-65. doi: 10.1182/blood-2005-09-3702. Epub 2005 Dec 8. Blood. 2006. PMID: 16339403 Free article.

4

Factor VIII gene mutations found by a comparative study of SSCP, DGGE and CMC and their analysis on a molecular model of factor VIII protein.

Schwaab R, Oldenburg J, Lalloz MR, Schwaab U, Pemberton S, Hanfland P, Brackmann HH, Tuddenham EG, Michaelides K. Schwaab R, et al. Among authors: hanfland p. Hum Genet. 1997 Dec;101(3):323-32. doi: 10.1007/s004390050636. Hum Genet. 1997. PMID: 9439662

5

Regulation of human factor IX expression using doxycycline-inducible gene expression system.

Srour MA, Fechner H, Wang X, Siemetzki U, Albert T, Oldenburg J, Hanfland P, Poller W, Brackmann HH, Schwaab R. Srour MA, et al. Among authors: hanfland p. Thromb Haemost. 2003 Sep;90(3):398-405. doi: 10.1160/TH03-01-0010. Thromb Haemost. 2003. PMID: 12958607

6

Assay discrepancy in mild haemophilia A due to a factor VIII missense mutation (Asn694Ile) in a large Danish family.

Schwaab R, Oldenburg J, Kemball-Cook G, Albert T, Juhler C, Hanfland P, Ingerslev J. Schwaab R, et al. Among authors: hanfland p. Br J Haematol. 2000 Jun;109(3):523-8. doi: 10.1046/j.1365-2141.2000.02021.x. Br J Haematol. 2000. PMID: 10886198 Free article.

7

Molecular genetics in haemophilia A.

Oldenburg J, Brackmann HH, Hanfland P, Schwaab R. Oldenburg J, et al. Among authors: hanfland p. Vox Sang. 2000;78 Suppl 2:33-8. Vox Sang. 2000. PMID: 10938924 Review.

8

Increased sensitivity of factor IX to phenprocoumon as a cause of bleeding in a patient with antiphospholipid antibody associated thrombosis.

Harbrecht U, Oldenburg J, Klein P, Weber D, Rockstroh J, Hanfland P. Harbrecht U, et al. Among authors: hanfland p. J Intern Med. 1998 Jan;243(1):73-7. doi: 10.1046/j.1365-2796.1998.00252.x. J Intern Med. 1998. PMID: 9487334 Free article.

9

Hemophilia treatment. Side effects during immune tolerance induction.

Brackmann HH, Schwaab R, Effenberger W, Hess L, Hanfland P, Oldenburg J. Brackmann HH, et al. Among authors: hanfland p. Haematologica. 2000 Oct;85(10 Suppl):75-7. Haematologica. 2000. PMID: 11187878 Review. No abstract available.

10

Analysis of expression kinetics and activity of a new B-domain truncated and full-length FVIII protein in three different cell lines.

Haack A, Schmitt C, Poller W, Oldenburg J, Hanfland P, Brackmann HH, Schwaab R. Haack A, et al. Among authors: hanfland p. Ann Hematol. 1999 Mar;78(3):111-6. doi: 10.1007/s002770050486. Ann Hematol. 1999. PMID: 10211752

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