Schambeck C - Search Results

1

Homozygous and compound-heterozygous type I plasminogen deficiency is a common cause of ligneous conjunctivitis.

Schuster V, Zeitler P, Seregard S, Ozcelik U, Anadol D, Luchtman-Jones L, Meire F, Mingers AM, Schambeck C, Kreth HW. Schuster V, et al. Among authors: schambeck c. Thromb Haemost. 2001 Jun;85(6):1004-10. Thromb Haemost. 2001. PMID: 11434676

2

Compound-heterozygous mutations in the plasminogen gene predispose to the development of ligneous conjunctivitis.

Schuster V, Seidenspinner S, Zeitler P, Escher C, Pleyer U, Bernauer W, Stiehm ER, Isenberg S, Seregard S, Olsson T, Mingers AM, Schambeck C, Kreth HW. Schuster V, et al. Among authors: schambeck c. Blood. 1999 May 15;93(10):3457-66. Blood. 1999. PMID: 10233898 Free article.

3

The impact of dalteparin (Fragmin) on thrombin generation in pregnant women with venous thromboembolism: significance of the factor V Leiden mutation.

Schambeck CM, Eberl E, Geisen U, Grossmann R, Keller F. Schambeck CM, et al. Thromb Haemost. 2001 May;85(5):782-6. Thromb Haemost. 2001. PMID: 11372668 Clinical Trial.

4

Selective screening for the Factor V Leiden mutation: is it advisable prior to the prescription of oral contraceptives?

Schambeck CM, Schwender S, Haubitz I, Geisen UE, Grossmann RE, Keller F. Schambeck CM, et al. Thromb Haemost. 1997 Dec;78(6):1480-3. Thromb Haemost. 1997. PMID: 9423798

5

Association of ADAMDEC1 haplotype with high factor VIII levels in venous thromboembolism.

Berger M, Moscatelli H, Kulle B, Luxembourg B, Blouin K, Spannagl M, Lindhoff-Last E, Schambeck CM. Berger M, et al. Thromb Haemost. 2008 May;99(5):905-8. doi: 10.1160/TH08-01-0059. Thromb Haemost. 2008. PMID: 18449420

6

Genetic risk factors in young adults with 'cryptogenic' ischemic cerebrovascular disease.

Grossmann R, Geisen U, Merati G, Müllges W, Schambeck CM, Walter U, Schwender S. Grossmann R, et al. Among authors: schambeck cm. Blood Coagul Fibrinolysis. 2002 Oct;13(7):583-90. doi: 10.1097/00001721-200210000-00002. Blood Coagul Fibrinolysis. 2002. PMID: 12439143

7

Familial clustering of high factor VIII levels in patients with venous thromboembolism.

Schambeck CM, Hinney K, Haubitz I, Mansouri Taleghani B, Wahler D, Keller F. Schambeck CM, et al. Arterioscler Thromb Vasc Biol. 2001 Feb;21(2):289-92. doi: 10.1161/01.atv.21.2.289. Arterioscler Thromb Vasc Biol. 2001. PMID: 11156867

8

CBS 844ins68, MTHFR TT677 and EPCR 4031ins23 genotypes in patients with deep-vein thrombosis.

Grossmann R, Schwender S, Geisen U, Schambeck C, Merati G, Walter U. Grossmann R, et al. Among authors: schambeck c. Thromb Res. 2002 Jul 15;107(1-2):13-5. doi: 10.1016/s0049-3848(02)00187-1. Thromb Res. 2002. PMID: 12413583

9

High factor VIII (FVIII) levels in venous thromboembolism: role of unbound FVIII.

Schambeck CM, Grossmann R, Zonnur S, Berger M, Teuchert K, Spahn A, Walter U. Schambeck CM, et al. Thromb Haemost. 2004 Jul;92(1):42-6. doi: 10.1160/TH04-02-0063. Thromb Haemost. 2004. PMID: 15213843

10

Molecular defects in the ABCA1 pathway affect platelet function.

Schmitz G, Schambeck CM. Schmitz G, et al. Pathophysiol Haemost Thromb. 2006;35(1-2):166-74. doi: 10.1159/000093563. Pathophysiol Haemost Thromb. 2006. PMID: 16855366 Review.

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