Tuddenham EG - Search Results

1

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

2

Haemophilia A diagnosis by simultaneous analysis of two variable dinucleotide tandem repeats within the factor VIII gene.

Lalloz MR, Schwaab R, McVey JH, Michaelides K, Tuddenham EG. Lalloz MR, et al. Among authors: tuddenham eg. Br J Haematol. 1994 Apr;86(4):804-9. doi: 10.1111/j.1365-2141.1994.tb04833.x. Br J Haematol. 1994. PMID: 7918076

3

A common ancestral glycoprotein (GP) 9 1828A>G (Asn45Ser) gene mutation occurring in European families from Australia and Northern Europe with Bernard-Soulier Syndrome (BSS).

Liang HP, Morel-Kopp MC, Clemetson JM, Clemetson KJ, Kekomaki R, Kroll H, Michaelides K, Tuddenham EG, Vanhoorelbeke K, Ward CM. Liang HP, et al. Among authors: tuddenham eg. Thromb Haemost. 2005 Sep;94(3):599-605. doi: 10.1160/TH05-03-0165. Thromb Haemost. 2005. PMID: 16268478

4

A G-->A substitution in an HNF I binding site in the human alpha-fetoprotein gene is associated with hereditary persistence of alpha-fetoprotein (HPAFP).

McVey JH, Michaelides K, Hansen LP, Ferguson-Smith M, Tilghman S, Krumlauf R, Tuddenham EG. McVey JH, et al. Among authors: tuddenham eg. Hum Mol Genet. 1993 Apr;2(4):379-84. doi: 10.1093/hmg/2.4.379. Hum Mol Genet. 1993. PMID: 7684942

5

Double heterozygosity for mutations in the platelet glycoprotein IX gene in three siblings with Bernard-Soulier syndrome.

Wright SD, Michaelides K, Johnson DJ, West NC, Tuddenham EG. Wright SD, et al. Among authors: tuddenham eg. Blood. 1993 May 1;81(9):2339-47. Blood. 1993. PMID: 8481514 Free article.

6

Platelet membrane glycoprotein Ibalpha gene -5T/C Kozak sequence polymorphism as an independent risk factor for the occurrence of coronary thrombosis.

Douglas H, Michaelides K, Gorog DA, Durante-Mangoni E, Ahmed N, Davies GJ, Tuddenham EG. Douglas H, et al. Among authors: tuddenham eg. Heart. 2002 Jan;87(1):70-4. doi: 10.1136/heart.87.1.70. Heart. 2002. PMID: 11751671 Free PMC 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

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

9

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

10

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

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