Goodeve A - Search Results

1

Late relapsing childhood lymphoblastic leukemia.

Vora A, Frost L, Goodeve A, Wilson G, Ireland RM, Lilleyman J, Eden T, Peake I, Richards S. Vora A, et al. Among authors: goodeve a. Blood. 1998 Oct 1;92(7):2334-7. Blood. 1998. PMID: 9746771 Free article.

2

Clonal stability in late-relapsing childhood lymphoblastic leukaemia.

Frost L, Goodeve A, Wilson G, Peake I, Barker H, Vora A. Frost L, et al. Among authors: goodeve a. Br J Haematol. 1997 Sep;98(4):992-4. doi: 10.1046/j.1365-2141.1997.3103129.x. Br J Haematol. 1997. PMID: 9326200 Free article.

3

A rapid and cost effective method for analysis of dinucleotide repeat polymorphisms in the factor VIII gene.

Goodeve AC, Tagariello G, Chuansumrit A, Preston FE, Peake IR. Goodeve AC, et al. Blood Coagul Fibrinolysis. 1996 Oct;7(7):672-7. doi: 10.1097/00001721-199610000-00002. Blood Coagul Fibrinolysis. 1996. PMID: 8958388

4

Are aberrant BCR--ABL transcripts more common than previously thought?

Wilson GA, Vandenberghe EA, Pollitt RC, Rees DC, Goodeve AC, Peake IR, Reilly JT. Wilson GA, et al. Among authors: goodeve ac. Br J Haematol. 2000 Dec;111(4):1109-11. doi: 10.1046/j.1365-2141.2000.02471.x. Br J Haematol. 2000. PMID: 11167748 Free article.

5

BCR-ABL transcript with an e19a2 (c3a2) junction in classical chronic myeloid leukemia.

Wilson G, Frost L, Goodeve A, Vandenberghe E, Peake I, Reilly J. Wilson G, et al. Among authors: goodeve a. Blood. 1997 Apr 15;89(8):3064. Blood. 1997. PMID: 9108430 Free article. No abstract available.

6

The molecular basis of hemophilia A: genotype-phenotype relationships and inhibitor development.

Goodeve AC, Peake IR. Goodeve AC, et al. Semin Thromb Hemost. 2003 Feb;29(1):23-30. doi: 10.1055/s-2003-37936. Semin Thromb Hemost. 2003. PMID: 12640561 Review.

7

Factor VIII gene rearrangements in patients with severe haemophilia A.

Goodeve AC, Preston FE, Peake IR. Goodeve AC, et al. Lancet. 1994 Feb 5;343(8893):329-30. doi: 10.1016/s0140-6736(94)91165-7. Lancet. 1994. PMID: 7905147

8

Two novel type 2N von Willebrand disease-causing mutations that result in defective factor VIII binding, multimerization, and secretion of von Willebrand factor.

Allen S, Abuzenadah AM, Blagg JL, Hinks J, Nesbitt IM, Goodeve AC, Gursel T, Ingerslev J, Peake IR, Daly ME. Allen S, et al. Among authors: goodeve ac. Blood. 2000 Mar 15;95(6):2000-7. Blood. 2000. PMID: 10706867 Free article.

9

A novel von Willebrand disease-causing mutation (Arg273Trp) in the von Willebrand factor propeptide that results in defective multimerization and secretion.

Allen S, Abuzenadah AM, Hinks J, Blagg JL, Gursel T, Ingerslev J, Goodeve AC, Peake IR, Daly ME. Allen S, et al. Among authors: goodeve ac. Blood. 2000 Jul 15;96(2):560-8. Blood. 2000. PMID: 10887119 Free article.

10

FLT3 internal tandem duplication mutations in adult acute myeloid leukaemia define a high-risk group.

Abu-Duhier FM, Goodeve AC, Wilson GA, Gari MA, Peake IR, Rees DC, Vandenberghe EA, Winship PR, Reilly JT. Abu-Duhier FM, et al. Among authors: goodeve ac. Br J Haematol. 2000 Oct;111(1):190-5. doi: 10.1046/j.1365-2141.2000.02317.x. Br J Haematol. 2000. PMID: 11091200 Free article.

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