Wulff K - Search Results

1

[Factors VII, VIII, IX, and X: molecular genetics and gene diagnosis].

Herrmann FH, Wulff K. Herrmann FH, et al. Among authors: wulff k. Hamostaseologie. 2004 May;24(2):94-107. doi: 10.1267/hamo04020094. Hamostaseologie. 2004. PMID: 15136874 Review. German.

2

[Structure and function of factor VIII and factor IX gene and molecular DNA diagnosis in hemophilia A and B].

Herrmann FH, Wehnert M, Wulff K. Herrmann FH, et al. Among authors: wulff k. Z Arztl Fortbild (Jena). 1988;82(22):1116-22. Z Arztl Fortbild (Jena). 1988. PMID: 2907834 Review. German. No abstract available.

3

Twenty-five novel mutations of the factor IX gene in haemophilia B.

Wulff K, Schröder W, Wehnert M, Herrmann FH. Wulff K, et al. Hum Mutat. 1995;6(4):346-8. doi: 10.1002/humu.1380060410. Hum Mutat. 1995. PMID: 8680410 No abstract available.

4

Haemophilia B in female twins caused by a point mutation in one factor IX gene and nonrandom inactivation patterns of the X-chromosomes.

Schröder W, Wulff K, Wollina K, Herrmann FH. Schröder W, et al. Among authors: wulff k. Thromb Haemost. 1997 Nov;78(5):1347-51. Thromb Haemost. 1997. PMID: 9408017

5

Molecular analysis of hemophilia B in Poland: 12 novel mutations of the factor IX gene.

Wulff K, Bykowska K, Lopaciuk S, Herrmann FH. Wulff K, et al. Acta Biochim Pol. 1999;46(3):721-6. Acta Biochim Pol. 1999. PMID: 10698280 Free article.

6

Twenty two novel mutations of the factor VII gene in factor VII deficiency.

Wulff K, Herrmann FH. Wulff K, et al. Hum Mutat. 2000;15(6):489-96. doi: 10.1002/1098-1004(200006)15:6<489::AID-HUMU1>3.0.CO;2-J. Hum Mutat. 2000. PMID: 10862079

7

Molecular biology and clinical manifestation of hereditary factor VII deficiency.

Herrmann FH, Wulff K, Auberger K, Aumann V, Bergmann F, Bergmann K, Bratanoff E, Franke D, Grundeis M, Kreuz W, Lenk H, Losonczy H, Maak B, Marx G, Mauz-Körholz C, Pollmann H, Serban M, Sutor A, Syrbe G, Vogel G, Weinstock N, Wenzel E, Wolf K. Herrmann FH, et al. Among authors: wulff k. Semin Thromb Hemost. 2000;26(4):393-400. doi: 10.1055/s-2000-8458. Semin Thromb Hemost. 2000. PMID: 11092214 Review.

8

Molecular analysis of FVIII gene in severe HA patients of Costa Rica.

Salazar-Sánchez L, Jiménez-Cruz G, Mendez M, Chaverri P, Alvarado P, Schröder W, Wulff K, Sandoval M, Herrmann FH, Pavlova A, Oldenburg J. Salazar-Sánchez L, et al. Among authors: wulff k. Hamostaseologie. 2010 Nov;30 Suppl 1:S150-2. Hamostaseologie. 2010. PMID: 21052611

9

Homozygous Factor X gene mutations Gly380Arg and Tyr163delAT are associated with perinatal intracranial hemorrhage.

Herrmann FH, Navarette M, Salazar-Sanchez L, Carillo JM, Auerswald G, Wulff K. Herrmann FH, et al. Among authors: wulff k. J Pediatr. 2005 Jan;146(1):128-30. doi: 10.1016/j.jpeds.2004.08.049. J Pediatr. 2005. PMID: 15644837

10

Clinical phenotypes and factor VII genotype in congenital factor VII deficiency.

Mariani G, Herrmann FH, Dolce A, Batorova A, Etro D, Peyvandi F, Wulff K, Schved JF, Auerswald G, Ingerslev J, Bernardi F; International Factor VII Deficiency Study Group. Mariani G, et al. Among authors: wulff k. Thromb Haemost. 2005 Mar;93(3):481-7. doi: 10.1160/TH04-10-0650. Thromb Haemost. 2005. PMID: 15735798

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