Herrmann FH - Search Results

1

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

Wulff K, Herrmann FH. Wulff K, et al. Among authors: herrmann fh. 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

2

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. J Pediatr. 2005 Jan;146(1):128-30. doi: 10.1016/j.jpeds.2004.08.049. J Pediatr. 2005. PMID: 15644837

3

Mutations of the iduronate-2-sulfatase (IDS) gene in patients with Hunter syndrome (mucopolysaccharidosis II).

Schröder W, Wulff K, Wehnert M, Seidlitz G, Herrmann FH. Schröder W, et al. Among authors: herrmann fh. Hum Mutat. 1994;4(2):128-31. doi: 10.1002/humu.1380040206. Hum Mutat. 1994. PMID: 7981716

4

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

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

5

Large-scale screening for factor V Leiden mutation in a north-eastern German population.

Schröder W, Koesling M, Wulff K, Wehnert M, Herrmann FH. Schröder W, et al. Among authors: herrmann fh. Haemostasis. 1996 Sep-Oct;26(5):233-6. doi: 10.1159/000217213. Haemostasis. 1996. PMID: 8894653

6

Six novel mutations in the emerin gene causing X-linked Emery-Dreifuss muscular dystrophy.

Wulff K, Parrish JE, Herrmann FH, Wehnert M. Wulff K, et al. Among authors: herrmann fh. Hum Mutat. 1997;9(6):526-30. doi: 10.1002/(SICI)1098-1004(1997)9:6<526::AID-HUMU5>3.0.CO;2-#. Hum Mutat. 1997. PMID: 9195226

7

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: herrmann fh. Thromb Haemost. 1997 Nov;78(5):1347-51. Thromb Haemost. 1997. PMID: 9408017

8

Identification of a novel large F9 gene mutation-an insertion of an Alu repeated DNA element in exon e of the factor 9 gene.

Wulff K, Gazda H, Schröder W, Robicka-Milewska R, Herrmann FH. Wulff K, et al. Among authors: herrmann fh. Hum Mutat. 2000 Mar;15(3):299. doi: 10.1002/(SICI)1098-1004(200003)15:3<299::AID-HUMU23>3.0.CO;2-1. Hum Mutat. 2000. PMID: 10679958 No abstract available.

9

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. Among authors: herrmann fh. Acta Biochim Pol. 1999;46(3):721-6. Acta Biochim Pol. 1999. PMID: 10698280

10

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. Semin Thromb Hemost. 2000;26(4):393-400. doi: 10.1055/s-2000-8458. Semin Thromb Hemost. 2000. PMID: 11092214 Review.

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