Bauer KA - Search Results

1

The G20210A prothrombin polymorphism is not associated with increased thromboembolic risk in a large protein C deficient kindred.

Bovill EG, Hasstedt SJ, Callas PW, Valliere JE, Scott BT, Bauer KA, Long GL. Bovill EG, et al. Among authors: bauer ka. Thromb Haemost. 2000 Mar;83(3):366-70. Thromb Haemost. 2000. PMID: 10744139

2

Heritability of plasma concentrations of clotting factors and measures of a prethrombotic state in a protein C-deficient family.

Vossen CY, Hasstedt SJ, Rosendaal FR, Callas PW, Bauer KA, Broze GJ, Hoogendoorn H, Long GL, Scott BT, Bovill EG. Vossen CY, et al. Among authors: bauer ka. J Thromb Haemost. 2004 Feb;2(2):242-7. doi: 10.1111/j.1538-7933.2003.00592.x. J Thromb Haemost. 2004. PMID: 14995985 Free article.

3

The clinical spectrum of heterozygous protein C deficiency in a large New England kindred.

Bovill EG, Bauer KA, Dickerman JD, Callas P, West B. Bovill EG, et al. Among authors: bauer ka. Blood. 1989 Feb 15;73(3):712-7. Blood. 1989. PMID: 2521802 Free article.

4

Prothrombin activation is increased among asymptomatic carriers of the prothrombin G20210A and factor V Arg506Gln mutations.

Bauer KA, Humphries S, Smillie B, Li L, Cooper JA, Barzegar S, Rosenberg RD, Miller GJ. Bauer KA, et al. Thromb Haemost. 2000 Sep;84(3):396-400. Thromb Haemost. 2000. PMID: 11019961

5

Factor V Leiden (FV R506Q) in families with inherited antithrombin deficiency.

van Boven HH, Reitsma PH, Rosendaal FR, Bayston TA, Chowdhury V, Bauer KA, Scharrer I, Conard J, Lane DA. van Boven HH, et al. Among authors: bauer ka. Thromb Haemost. 1996 Mar;75(3):417-21. Thromb Haemost. 1996. PMID: 8701400

6

Two multiplex PCR-based DNA assays for the thrombosis risk factors prothrombin G20210A and coagulation factor V G1691A polymorphisms.

Xu X, Bauer KA, Griffin JH. Xu X, et al. Among authors: bauer ka. Thromb Res. 1999 Mar 15;93(6):265-9. doi: 10.1016/s0049-3848(98)00178-9. Thromb Res. 1999. PMID: 10093967

7

Hormonal factors and risk of recurrent venous thrombosis: the prevention of recurrent venous thromboembolism trial.

Cushman M, Glynn RJ, Goldhaber SZ, Moll S, Bauer KA, Deitcher S, Shrivastava S, Ridker PM. Cushman M, et al. Among authors: bauer ka. J Thromb Haemost. 2006 Oct;4(10):2199-203. doi: 10.1111/j.1538-7836.2006.02140.x. Epub 2006 Jul 26. J Thromb Haemost. 2006. PMID: 16869933 Free article. Clinical Trial.

8

Management of thrombophilia.

Bauer KA. Bauer KA. J Thromb Haemost. 2003 Jul;1(7):1429-34. doi: 10.1046/j.1538-7836.2003.00274.x. J Thromb Haemost. 2003. PMID: 12871277 Free article. Review.

9

Automated detection of the G20210A prothrombin mutation using the LCx microparticle enzyme immunoassay.

Gilchrist A, Solomon N, Erickson D, Sikand A, Bauer KA, Kruskall MS, Kocher O. Gilchrist A, et al. Among authors: bauer ka. Clin Chim Acta. 2001 Dec;314(1-2):249-54. doi: 10.1016/s0009-8981(01)00655-6. Clin Chim Acta. 2001. PMID: 11718704 Clinical Trial.

10

A functional haplotype in the 5' flanking region of the factor VII gene is associated with an increased risk of coronary heart disease.

Carew JA, Basso F, Miller GJ, Hawe E, Jackson AA, Humphries SE, Bauer KA. Carew JA, et al. Among authors: bauer ka. J Thromb Haemost. 2003 Oct;1(10):2179-85. doi: 10.1046/j.1538-7836.2003.00424.x. J Thromb Haemost. 2003. PMID: 14521602 Free article.

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