Tuddenham EG - Search Results

1

Pharmacodynamic resistance to warfarin associated with a Val66Met substitution in vitamin K epoxide reductase complex subunit 1.

Harrington DJ, Underwood S, Morse C, Shearer MJ, Tuddenham EG, Mumford AD. Harrington DJ, et al. Among authors: tuddenham eg. Thromb Haemost. 2005 Jan;93(1):23-6. doi: 10.1160/TH04-08-0540. Thromb Haemost. 2005. PMID: 15630486

2

A novel missense mutation in ABCA1 results in altered protein trafficking and reduced phosphatidylserine translocation in a patient with Scott syndrome.

Albrecht C, McVey JH, Elliott JI, Sardini A, Kasza I, Mumford AD, Naoumova RP, Tuddenham EG, Szabo K, Higgins CF. Albrecht C, et al. Among authors: tuddenham eg. Blood. 2005 Jul 15;106(2):542-9. doi: 10.1182/blood-2004-05-2056. Epub 2005 Mar 24. Blood. 2005. PMID: 15790791 Free article.

3

Characterisation of lymphocyte responses to Ca2+ in Scott syndrome.

Elliott JI, Mumford AD, Albrecht C, Collins PW, Giddings JC, Higgins CF, Tuddenham EG, McVey JH. Elliott JI, et al. Among authors: tuddenham eg. Thromb Haemost. 2004 Feb;91(2):412-5. Thromb Haemost. 2004. PMID: 14961172 Review. No abstract available.

4

Factor V I359T: a novel mutation associated with thrombosis and resistance to activated protein C.

Mumford AD, McVey JH, Morse CV, Gomez K, Steen M, Norstrom EA, Tuddenham EG, Dahlback B, Bolton-Maggs PH. Mumford AD, et al. Among authors: tuddenham eg. Br J Haematol. 2003 Nov;123(3):496-501. doi: 10.1046/j.1365-2141.2003.04624.x. Br J Haematol. 2003. PMID: 14617013 Free article.

5

Factor VII deficiency and the FVII mutation database.

McVey JH, Boswell E, Mumford AD, Kemball-Cook G, Tuddenham EG. McVey JH, et al. Among authors: tuddenham eg. Hum Mutat. 2001;17(1):3-17. doi: 10.1002/1098-1004(2001)17:1<3::AID-HUMU2>3.0.CO;2-V. Hum Mutat. 2001. PMID: 11139238 Review.

6

Optimizing warfarin reversal--an ex vivo study.

Gatt A, Riddell A, van Veen JJ, Kitchen S, Tuddenham EG, Makris M. Gatt A, et al. Among authors: tuddenham eg. J Thromb Haemost. 2009 Jul;7(7):1123-7. doi: 10.1111/j.1538-7836.2009.03435.x. J Thromb Haemost. 2009. PMID: 19575759 Free article.

7

Characterisation of blood coagulation factor XI T475I.

McVey JH, Lal K, Imanaka Y, Kemball-Cook G, Bolton-Maggs PH, Tuddenham EG. McVey JH, et al. Among authors: tuddenham eg. Thromb Haemost. 2005 Jun;93(6):1082-8. doi: 10.1160/TH05-01-0051. Thromb Haemost. 2005. PMID: 15968392

8

Live birth following the first mutation specific pre-implantation genetic diagnosis for haemophilia A.

Michaelides K, Tuddenham EG, Turner C, Lavender B, Lavery SA. Michaelides K, et al. Among authors: tuddenham eg. Thromb Haemost. 2006 Feb;95(2):373-9. doi: 10.1160/TH05-08-0574. Thromb Haemost. 2006. PMID: 16493501

9

Factor VIII S373L: mutation at P1' site confers thrombin cleavage resistance, causing mild haemophilia A.

Johnson DJ, Pemberton S, Acquila M, Mori PG, Tuddenham EG, O'Brien DP. Johnson DJ, et al. Among authors: tuddenham eg. Thromb Haemost. 1994 Apr;71(4):428-33. Thromb Haemost. 1994. PMID: 8052958

10

Analysis of the F8 gene in individuals with high plasma factor VIII: C levels and associated venous thrombosis.

Mansvelt EP, Laffan M, McVey JH, Tuddenham EG. Mansvelt EP, et al. Among authors: tuddenham eg. Thromb Haemost. 1998 Oct;80(4):561-5. Thromb Haemost. 1998. PMID: 9798969

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