Cooper PC - Search Results

1

Recommendations for clinical laboratory testing for antithrombin deficiency; Communication from the SSC of the ISTH.

Van Cott EM, Orlando C, Moore GW, Cooper PC, Meijer P, Marlar R; Subcommittee on Plasma Coagulation Inhibitors. Van Cott EM, et al. Among authors: cooper pc. J Thromb Haemost. 2020 Jan;18(1):17-22. doi: 10.1111/jth.14648. J Thromb Haemost. 2020. PMID: 31894660 Free article.

2

Recommendations for clinical laboratory testing for protein C deficiency, for the subcommittee on plasma coagulation inhibitors of the ISTH.

Cooper PC, Pavlova A, Moore GW, Hickey KP, Marlar RA. Cooper PC, et al. J Thromb Haemost. 2020 Feb;18(2):271-277. doi: 10.1111/jth.14667. J Thromb Haemost. 2020. PMID: 31999059 Free article.

3

Transient inherited antithrombin deficiency: a real phenomenon?

Daly ME, Cooper PC, Hickey KP, Jennings I, Makris M. Daly ME, et al. Among authors: cooper pc. 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.

4

The phenotypic and genetic assessment of antithrombin deficiency.

Cooper PC, Coath F, Daly ME, Makris M. Cooper PC, et al. Int J Lab Hematol. 2011 Jun;33(3):227-37. doi: 10.1111/j.1751-553X.2011.01307.x. Epub 2011 Mar 15. Int J Lab Hematol. 2011. PMID: 21401902 Review.

5

Thrombin generation assays are superior to traditional tests in assessing anticoagulation reversal in vitro.

Gatt A, van Veen JJ, Woolley AM, Kitchen S, Cooper P, Makris M. Gatt A, et al. Thromb Haemost. 2008 Aug;100(2):350-5. Thromb Haemost. 2008. PMID: 18690358

6

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

7

The phenotypic and genetic assessment of protein C deficiency.

Cooper PC, Hill M, Maclean RM. Cooper PC, et al. Int J Lab Hematol. 2012 Aug;34(4):336-46. doi: 10.1111/j.1751-553X.2012.01401.x. Epub 2012 Feb 9. Int J Lab Hematol. 2012. PMID: 22321166 Review.

8

Quality in molecular biology testing for inherited thrombophilia disorders.

Cooper PC, Goodeve AC, Beauchamp NJ. Cooper PC, et al. Semin Thromb Hemost. 2012 Sep;38(6):600-12. doi: 10.1055/s-0032-1321491. Epub 2012 Aug 20. Semin Thromb Hemost. 2012. PMID: 22907670 Review.

9

An overview of methods for detection of factor V Leiden and the prothrombin G20210A mutations.

Cooper PC, Rezende SM. Cooper PC, et al. Int J Lab Hematol. 2007 Jun;29(3):153-62. doi: 10.1111/j.1751-553X.2007.00892.x. Int J Lab Hematol. 2007. PMID: 17474891 Review.

10

Screening for thrombophilia: a laboratory perspective.

Jennings I, Cooper P. Jennings I, et al. Br J Biomed Sci. 2003;60(1):39-51. doi: 10.1080/09674845.2003.11783675. Br J Biomed Sci. 2003. PMID: 12680634 Review.

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