Callas PW - Search Results

1

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: callas pw. 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.

2

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. Blood. 1989 Feb 15;73(3):712-7. Blood. 1989. PMID: 2521802 Free article.

3

Plasma levels of factors II, VII and X and their relationship to the international normalized ratio during chronic warfarin therapy.

Lind SE, Callas PW, Golden EA, Joyner KA Jr, Ortel TL. Lind SE, et al. Among authors: callas pw. Blood Coagul Fibrinolysis. 1997 Jan;8(1):48-53. doi: 10.1097/00001721-199701000-00008. Blood Coagul Fibrinolysis. 1997. PMID: 9105637

4

An unknown genetic defect increases venous thrombosis risk, through interaction with protein C deficiency.

Hasstedt SJ, Bovill EG, Callas PW, Long GL. Hasstedt SJ, et al. Among authors: callas pw. Am J Hum Genet. 1998 Aug;63(2):569-76. doi: 10.1086/301947. Am J Hum Genet. 1998. PMID: 9683579 Free PMC article.

5

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: callas pw. Thromb Haemost. 2000 Mar;83(3):366-70. Thromb Haemost. 2000. PMID: 10744139

6

Genetic screening of candidate genes for a prothrombotic interaction with type I protein C deficiency in a large kindred.

Scott BT, Bovill EG, Callas PW, Hasstedt SJ, Leppert MF, Valliere JE, Varvil TS, Long GL. Scott BT, et al. Among authors: callas pw. Thromb Haemost. 2001 Jan;85(1):82-7. Thromb Haemost. 2001. PMID: 11204593

7

Evidence of a founder effect for the protein C gene 3363 inserted C mutation in thrombophilic pedigrees of French origin.

Couture P, Bovill EG, Demers C, Simard J, Delage R, Scott BT, Valliere JE, Callas PW, Jomphe M, Rosendaal FR, Aiach M, Long GL. Couture P, et al. Among authors: callas pw. Thromb Haemost. 2001 Oct;86(4):1000-6. Thromb Haemost. 2001. PMID: 11686315

8

Longitudinal stability of coagulation, fibrinolysis, and inflammation factors in stored plasma samples.

Lewis MR, Callas PW, Jenny NS, Tracy RP. Lewis MR, et al. Among authors: callas pw. Thromb Haemost. 2001 Dec;86(6):1495-500. Thromb Haemost. 2001. PMID: 11776319

9

Characterization of the human prostaglandin H synthase 1 gene (PTGS1): exclusion by genetic linkage analysis as a second modifier gene in familial thrombosis.

Scott BT, Hasstedt SJ, Bovill EG, Callas PW, Valliere JE, Wang L, Wu KK, Long GL. Scott BT, et al. Among authors: callas pw. Blood Coagul Fibrinolysis. 2002 Sep;13(6):519-31. doi: 10.1097/00001721-200209000-00007. Blood Coagul Fibrinolysis. 2002. PMID: 12192304

10

Inter-relation of coagulation factors and d-dimer levels in healthy individuals.

Van Hylckama Vlieg A, Callas PW, Cushman M, Bertina RM, Rosendaal FR. Van Hylckama Vlieg A, et al. Among authors: callas pw. J Thromb Haemost. 2003 Mar;1(3):516-22. doi: 10.1046/j.1538-7836.2003.00080.x. J Thromb Haemost. 2003. PMID: 12871460 Free article.

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