Long GL - Search Results

1

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: long gl. Thromb Haemost. 2001 Oct;86(4):1000-6. Thromb Haemost. 2001. PMID: 11686315

2

No effect of the prothrombin G20210A mutation on protein C activation in a large kindred with type I protein C deficiency.

Vossen CY, Strandberg K, Stenflo J, Rosendaal FR, Callas PW, Long GL, Bovill EG. Vossen CY, et al. Among authors: long gl. Blood Coagul Fibrinolysis. 2004 Oct;15(7):573-6. doi: 10.1097/00001721-200410000-00007. Blood Coagul Fibrinolysis. 2004. PMID: 15389124

3

Exclusion of the alpha2 subunit of platelet-activating factor acetylhydrolase 1b (PAFAH1B2) as a prothrombotic gene in a protein C-deficient kindred and population-based case-control sample.

Hasstedt SJ, Scott BT, Rosendaal FR, Callas PW, Vossen CY, Long GL, Bovill EG. Hasstedt SJ, et al. Among authors: long gl. Thromb Haemost. 2007 Sep;98(3):587-92. Thromb Haemost. 2007. PMID: 17849047

4

Hereditary thrombophilia as a model for multigenic disease.

Bovill EG, Hasstedt SJ, Leppert MF, Long GL. Bovill EG, et al. Among authors: long gl. Thromb Haemost. 1999 Aug;82(2):662-6. Thromb Haemost. 1999. PMID: 10605765 Review. No abstract available.

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: long gl. 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: long gl. Thromb Haemost. 2001 Jan;85(1):82-7. Thromb Haemost. 2001. PMID: 11204593

7

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: long gl. 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.

8

Genome scan of venous thrombosis in a pedigree with protein C deficiency.

Hasstedt SJ, Scott BT, Callas PW, Vossen CY, Rosendaal FR, Long GL, Bovill EG. Hasstedt SJ, et al. Among authors: long gl. J Thromb Haemost. 2004 Jun;2(6):868-73. doi: 10.1111/j.1538-7836.2004.00663.x. J Thromb Haemost. 2004. PMID: 15140118 Free article.

9

Chronic venous abnormalities in symptomatic and asymptomatic protein C deficiency.

Emmerich J, Vossen CY, Callas PW, Demers C, Naud S, Long GL, Couture P, Rosendaal FR, Bovill EG. Emmerich J, et al. Among authors: long gl. J Thromb Haemost. 2005 Jul;3(7):1428-31. doi: 10.1111/j.1538-7836.2005.01452.x. J Thromb Haemost. 2005. PMID: 15978099 Free article.

10

A genetic basis for the interrelation of coagulation factors.

Vossen CY, Callas PW, Hasstedt SJ, Long GL, Rosendaal FR, Bovill EG. Vossen CY, et al. Among authors: long gl. J Thromb Haemost. 2007 Sep;5(9):1930-5. doi: 10.1111/j.1538-7836.2007.02678.x. J Thromb Haemost. 2007. PMID: 17723132 Free article.

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