Makris M - Search Results

1

Establishment of the 1st International Genetic Reference Panel for Factor V Leiden, human gDNA.

Gray E, Hawkins JR, Morrison M, Hawkins M, Byrne E, Kitchen S, Jennings I, Makris M, Preston FE, Metcalfe P. Gray E, et al. Among authors: makris m. Thromb Haemost. 2006 Aug;96(2):215-9. Thromb Haemost. 2006. PMID: 16894467

2

SSC/ISTH classification of hemophilia A: can hemophilia center laboratories achieve the new criteria?

Preston FE, Kitchen S, Jennings I, Woods TA, Makris M. Preston FE, et al. Among authors: makris m. J Thromb Haemost. 2004 Feb;2(2):271-4. doi: 10.1046/j.1538-7836.2003.00447.x. J Thromb Haemost. 2004. PMID: 14995989 Free article.

3

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: makris m. Thromb Haemost. 1998 Jun;79(6):1086-91. Thromb Haemost. 1998. PMID: 9657428

4

Sensitivity of functional protein S assays to protein S deficiency: a comparative study of three commercial kits.

Jennings I, Kitchen S, Cooper P, Makris M, Preston FE. Jennings I, et al. Among authors: makris m. J Thromb Haemost. 2003 May;1(5):1112-4. doi: 10.1046/j.1538-7836.2003.00215.x. J Thromb Haemost. 2003. PMID: 12871384 Free article. No abstract available.

5

Transient inherited antithrombin deficiency: a real phenomenon?

Daly ME, Cooper PC, Hickey KP, Jennings I, Makris M. Daly ME, et al. Among authors: makris m. Thromb Haemost. 2017 Feb 28;117(3):642-643. doi: 10.1160/TH16-10-0791. Epub 2016 Dec 15. Thromb Haemost. 2017. PMID: 27975105 Free article. No abstract available.

6

Potential thrombogenicity of heat-treated prothrombin complex concentrates in Haemophilia B.

Hampton KK, Makris M, Kitchen S, Preston FE. Hampton KK, et al. Among authors: makris m. Blood Coagul Fibrinolysis. 1991 Oct;2(5):637-41. doi: 10.1097/00001721-199110000-00008. Blood Coagul Fibrinolysis. 1991. PMID: 1782333

7

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: makris m. Blood. 1996 Sep 1;88(5):1700-7. Blood. 1996. PMID: 8781426 Free article.

8

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. Thromb Haemost. 1997 Dec;78(6):1426-9. Thromb Haemost. 1997. PMID: 9423788

9

Major structural defects in the antithrombin gene in four families with type I antithrombin deficiency--partial/complete deletions and rearrangement of the antithrombin gene.

Beauchamp NJ, Makris M, Preston FE, Peake IR, Daly ME. Beauchamp NJ, et al. Among authors: makris m. Thromb Haemost. 2000 May;83(5):715-21. Thromb Haemost. 2000. PMID: 10823268

10

Protein C deficiency screening using a thrombin generation assay - an upgrade.

Gatt A, van Veen JJ, Cooper P, Kitchen S, Makris M. Gatt A, et al. Among authors: makris m. Thromb Haemost. 2007 Sep;98(3):691-2. Thromb Haemost. 2007. PMID: 17849065 No abstract available.

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