Coulthard S - Search Results

1

Molecular analysis of transient cytogenetic relapse after allogeneic bone marrow transplantation for chronic myeloid leukaemia.

Lin F, Kirkland MA, van Rhee FV, Chase A, Coulthard S, Bungey J, Goldman JM, Cross NC. Lin F, et al. Among authors: coulthard s. Bone Marrow Transplant. 1996 Dec;18(6):1147-52. Bone Marrow Transplant. 1996. PMID: 8971386

2

Non-random involvement of chromosome 13 in patients with persistent or relapsed disease after bone-marrow transplantation for chronic myeloid leukemia.

Chase A, Pickard J, Szydlo R, Coulthard S, Goldman JM, Cross NC. Chase A, et al. Among authors: coulthard s. Genes Chromosomes Cancer. 2000 Mar;27(3):278-84. Genes Chromosomes Cancer. 2000. PMID: 10679917

3

Two cases of inv(8)(p11q13) in AML with erythrophagocytosis: a new cytogenetic variant.

Coulthard S, Chase A, Orchard K, Watmore A, Vora A, Goldman JM, Swirsky DM. Coulthard S, et al. Br J Haematol. 1998 Mar;100(3):561-3. doi: 10.1046/j.1365-2141.1998.00587.x. Br J Haematol. 1998. PMID: 9504640 Free article.

4

Chromosomal breakage analysis in dyskeratosis congenita peripheral blood lymphocytes.

Coulthard S, Chase A, Pickard J, Goldman J, Dokal I. Coulthard S, et al. Br J Haematol. 1998 Sep;102(5):1162-4. doi: 10.1046/j.1365-2141.1998.00893.x. Br J Haematol. 1998. PMID: 9753038 Free article.

5

Positive diepoxybutane test in only one of two brothers found to be compound heterozygotes for Fanconi's anaemia complementation group C mutations.

Dokal I, Chase A, Morgan NV, Coulthard S, Hall G, Mathew CG, Roberts I. Dokal I, et al. Among authors: coulthard s. Br J Haematol. 1996 Jun;93(4):813-6. doi: 10.1046/j.1365-2141.1996.d01-1726.x. Br J Haematol. 1996. PMID: 8703809

6

Abnormalities of chromosome band 8p11 in leukemia: two clinical syndromes can be distinguished on the basis of MOZ involvement.

Aguiar RC, Chase A, Coulthard S, Macdonald DH, Carapeti M, Reiter A, Sohal J, Lennard A, Goldman JM, Cross NC. Aguiar RC, et al. Among authors: coulthard s. Blood. 1997 Oct 15;90(8):3130-5. Blood. 1997. PMID: 9376594 Free article.

7

The relationship between thiopurine methyltransferase activity and genotype in blasts from patients with acute leukemia.

Coulthard SA, Howell C, Robson J, Hall AG. Coulthard SA, et al. Blood. 1998 Oct 15;92(8):2856-62. Blood. 1998. PMID: 9763570 Free article.

8

A comparison of molecular and enzyme-based assays for the detection of thiopurine methyltransferase mutations.

Coulthard SA, Rabello C, Robson J, Howell C, Minto L, Middleton PG, Gandhi MK, Jackson G, McLelland J, O'Brien H, Smith S, Reid MM, Pearson AD, Hall AG. Coulthard SA, et al. Br J Haematol. 2000 Sep;110(3):599-604. doi: 10.1046/j.1365-2141.2000.02218.x. Br J Haematol. 2000. PMID: 10997970 Free article.

9

Expression levels of asparagine synthetase in blasts from children and adults with acute lymphoblastic leukaemia.

Leslie M, Case MC, Hall AG, Coulthard SA. Leslie M, et al. Among authors: coulthard sa. Br J Haematol. 2006 Mar;132(6):740-2. doi: 10.1111/j.1365-2141.2005.05945.x. Br J Haematol. 2006. PMID: 16487174 Free article.

10

Thiopurine methyltransferase genetics is not a major risk factor for secondary malignant neoplasms after treatment of childhood acute lymphoblastic leukemia on Berlin-Frankfurt-Münster protocols.

Stanulla M, Schaeffeler E, Möricke A, Coulthard SA, Cario G, Schrauder A, Kaatsch P, Dördelmann M, Welte K, Zimmermann M, Reiter A, Eichelbaum M, Riehm H, Schrappe M, Schwab M. Stanulla M, et al. Blood. 2009 Aug 13;114(7):1314-8. doi: 10.1182/blood-2008-12-193250. Epub 2009 Jun 17. Blood. 2009. PMID: 19535798 Free article.

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