Tait RC - Search Results

1

Antithrombin alfa in hereditary antithrombin deficient patients: A phase 3 study of prophylactic intravenous administration in high risk situations.

Tiede A, Tait RC, Shaffer DW, Baudo F, Boneu B, Dempfle CE, Horellou MH, Klamroth R, Lazarchick J, Mumford AD, Schulman S, Shiach C, Bonfiglio LJ, Frieling JT, Conard J, von Depka M. Tiede A, et al. Among authors: tait rc. Thromb Haemost. 2008 Mar;99(3):616-22. doi: 10.1160/TH07-08-0489. Thromb Haemost. 2008. PMID: 18327412 Clinical Trial.

2

Perioperative and peripartum prevention of venous thromboembolism in patients with hereditary antithrombin deficiency using recombinant antithrombin therapy.

Paidas MJ, Forsyth C, Quéré I, Rodger M, Frieling JT, Tait RC; Recombinant Human Antithrombin Study Group. Paidas MJ, et al. Among authors: tait rc. Blood Coagul Fibrinolysis. 2014 Jul;25(5):444-50. doi: 10.1097/MBC.0000000000000076. Blood Coagul Fibrinolysis. 2014. PMID: 24686101

3

New Inhibitors in the Ageing Population: A Retrospective, Observational, Cohort Study of New Inhibitors in Older People with Hemophilia.

Astermark J, Ay C, Carvalho M, D'Oiron R, Moerloose P, Dolan G, Fontana P, Hermans C, Holme PA, Katsarou O, Kenet G, Klamroth R, Mancuso ME, Marquardt N, Núñez R, Pabinger I, Tait R, Valk PV. Astermark J, et al. Thromb Haemost. 2022 Jun;122(6):905-912. doi: 10.1055/a-1642-4067. Epub 2021 Nov 5. Thromb Haemost. 2022. PMID: 34507368

4

A new pedigree with thrombomodulin-associated coagulopathy in which delayed fibrinolysis is partially attenuated by co-inherited TAFI deficiency.

Westbury SK, Whyte CS, Stephens J, Downes K, Turro E, Claesen K, Mertens JC, Hendriks D, Latif AL, Leishman EJ; NIHR BioResource; Mutch NJ, Tait RC, Mumford AD. Westbury SK, et al. Among authors: tait rc. J Thromb Haemost. 2020 Sep;18(9):2209-2214. doi: 10.1111/jth.14990. Epub 2020 Jul 23. J Thromb Haemost. 2020. PMID: 32634856 Free article.

5

Low thrombosis rate seen in blood donors and their relatives with inherited deficiencies of antithrombin and protein C: correlation with type of defect, family history, and absence of the factor V Leiden mutation.

McColl M, Tait RC, Walker ID, Perry DJ, McCall F, Conkie JA. McColl M, et al. Among authors: tait rc. Blood Coagul Fibrinolysis. 1996 Oct;7(7):689-94. doi: 10.1097/00001721-199610000-00005. Blood Coagul Fibrinolysis. 1996. PMID: 8958391

6

Superficial vein thrombosis: incidence in association with pregnancy and prevalence of thrombophilic defects.

McColl MD, Ramsay JE, Tait RC, Walker ID, McCall F, Conkie JA, Carty MJ, Greer IA. McColl MD, et al. Among authors: tait rc. Thromb Haemost. 1998 Apr;79(4):741-2. Thromb Haemost. 1998. PMID: 9569184

7

Isolated familial plasminogen deficiency may not be a risk factor for thrombosis.

Tait RC, Walker ID, Conkie JA, Islam SI, McCall F. Tait RC, et al. Thromb Haemost. 1996 Dec;76(6):1004-8. Thromb Haemost. 1996. PMID: 8972025

8

Risk factors for pregnancy associated venous thromboembolism.

McColl MD, Ramsay JE, Tait RC, Walker ID, McCall F, Conkie JA, Carty MJ, Greer IA. McColl MD, et al. Among authors: tait rc. Thromb Haemost. 1997 Oct;78(4):1183-8. Thromb Haemost. 1997. PMID: 9364982

9

Type I antithrombin deficiency: five novel mutations associated with thrombosis.

Daly M, Perry DJ, Bruce DB, Harper PL, Tait RC, Walker ID, Mayne EE, Daly HM, Brown K, Carrell RW. Daly M, et al. Among authors: tait rc. Blood Coagul Fibrinolysis. 1996 Mar;7(2):139-43. Blood Coagul Fibrinolysis. 1996. PMID: 8735803

10

Hereditary and acquired antithrombin deficiency: epidemiology, pathogenesis and treatment options.

Maclean PS, Tait RC. Maclean PS, et al. Among authors: tait rc. Drugs. 2007;67(10):1429-40. doi: 10.2165/00003495-200767100-00005. Drugs. 2007. PMID: 17600391 Review.

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