Preston FE - Search Results

1

Familial thrombophilia: genetic risk factors and management.

Makris M, Rosendaal FR, Preston FE. Makris M, et al. Among authors: preston fe. J Intern Med Suppl. 1997;740:9-15. J Intern Med Suppl. 1997. PMID: 9350176 Free article. Review.

2

Increased fetal loss in women with heritable thrombophilia.

Preston FE, Rosendaal FR, Walker ID, Briët E, Berntorp E, Conard J, Fontcuberta J, Makris M, Mariani G, Noteboom W, Pabinger I, Legnani C, Scharrer I, Schulman S, van der Meer FJ. Preston FE, et al. Lancet. 1996 Oct 5;348(9032):913-6. doi: 10.1016/s0140-6736(96)04125-6. Lancet. 1996. PMID: 8843809 Free article.

3

Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophilia.

Makris M, Preston FE, Beauchamp NJ, Cooper PC, Daly ME, Hampton KK, Bayliss P, Peake IR, Miller GJ. Makris M, et al. Among authors: preston fe. Thromb Haemost. 1997 Dec;78(6):1426-9. Thromb Haemost. 1997. PMID: 9423788

4

Recurrence rate after a first venous thrombosis in patients with familial thrombophilia.

Vossen CY, Walker ID, Svensson P, Souto JC, Scharrer I, Preston FE, Palareti G, Pabinger I, van der Meer FJ, Makris M, Fontcuberta J, Conard J, Rosendaal FR. Vossen CY, et al. Among authors: preston fe. Arterioscler Thromb Vasc Biol. 2005 Sep;25(9):1992-7. doi: 10.1161/01.ATV.0000174806.76629.7b. Epub 2005 Jun 23. Arterioscler Thromb Vasc Biol. 2005. PMID: 15976329

5

Chronic hepatitis in haemophilia.

Makris M, Preston FE. Makris M, et al. Among authors: preston fe. Blood Rev. 1993 Dec;7(4):243-50. doi: 10.1016/0268-960x(93)90011-r. Blood Rev. 1993. PMID: 7510563 Review.

6

Molecular basis of protein S deficiency in three families also showing independent inheritance of factor V leiden.

Beauchamp NJ, Daly ME, Cooper PC, Makris M, Preston FE, Peake IR. Beauchamp NJ, et al. Among authors: preston fe. Blood. 1996 Sep 1;88(5):1700-7. Blood. 1996. PMID: 8781426 Free article.

7

In vivo coagulation activation following infusion of highly purified factor XI concentrate.

Richards EM, Makris MM, Cooper P, Preston FE. Richards EM, et al. Among authors: preston fe. Br J Haematol. 1997 Feb;96(2):293-7. doi: 10.1046/j.1365-2141.1997.d01-2015.x. Br J Haematol. 1997. PMID: 9029015 Free article.

8

The successful use of protein C concentrate during pregnancy in a patient with type 1 protein C deficiency, previous thrombosis and recurrent fetal loss.

Richards EM, Makris M, Preston FE. Richards EM, et al. Among authors: preston fe. Br J Haematol. 1997 Sep;98(3):660-1. doi: 10.1046/j.1365-2141.1997.2873100.x. Br J Haematol. 1997. PMID: 9332323 Free article.

9

A novel mutation in intron K of the PROS1 gene causes aberrant RNA splicing and is a common cause of protein S deficiency in a UK thrombophilia cohort.

Beauchamp NJ, Daly ME, Makris M, Preston FE, Peake IR. Beauchamp NJ, et al. Among authors: preston fe. Thromb Haemost. 1998 Jun;79(6):1086-91. Thromb Haemost. 1998. PMID: 9657428

10

Acute liver failure induced by alcohol and paracetamol in an HCV-infected haemophiliac.

Leach M, Makris M, Gleeson DC, Preston FE. Leach M, et al. Among authors: preston fe. Br J Haematol. 1998 Dec;103(3):891-3. doi: 10.1046/j.1365-2141.1998.01046.x. Br J Haematol. 1998. PMID: 9858252 Free article.

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