Dr Colin Steward
Reader in Stem Cell Transplantation
Bristol Royal Hospital for Children, Department of Haematology, Oncology and BMT,
Level 6, Upper Maudlin Street, Bristol, BS2 8BJ
phone: +44 (0)117 342 8044
email: colin.steward@bristol.ac.uk
Research interests
- Barth Syndrome
- Identification, development of diagnostic tests and improving management of transplant complications
- Identification of new or rare genetic diseases and areas of under-diagnosis
Selected publications
- Steward, C.G., Newbury-Ecob, R.A., Hastings, R., Smithson, S.F., Tsai-Goodman, B., Quarrell, O.W., Kulik, W., Wanders, R., Pennock, M., Williams, M., Cresswell, J.L., Gonzalez, I.L., Brennan, P. (2010) Barth syndrome: an X-linked cause of fetal cardiomyopathy and stillbirth. Prenat. Diagn. 30(10), 970-976.
- Mansour, S., Connell, F., Steward, C., Ostergaard, P., Brice, G., Smithson, S., Lunt, P., Jeffery, S., Dokal, I., Vulliamy, T., Gibson, B., Hodgson, S., Cottrell, S., Kiely, L., Tinworth, L., Kalidas, K., Mufti, G., Cornish, J., Keenan, R., Mortimer, P., Murday, V. (2010) Lymphoedema Research Consortium. Emberger syndrome-primary lymphedema with myelodysplasia: report of seven new cases. Am. J. Med. Genet. A. 152A(9), 2287-2296.
- Steward, C.G. (2010) Hematopoietic stem cell transplantation for osteopetrosis. Pediatr. Clin. North Am. 57(1), 171-180.
- Hastings, R., Steward, C., Tsai-Goodman, B., Newbury-Ecob, R. (2009) Dysmorphology of Barth syndrome. Clin. Dysmorphol. 18(4), 185-187.
- Houtkooper, R.H., Rodenburg, R.J., Thiels, C., van Lenthe, H., Stet, F., Poll-The, B.T., Stone, J.E., Steward, C.G., Wanders, R.J., Smeitink, J., Kulik, W., Vaz, F.M. (2009) Cardiolipin and monolysocardiolipin analysis in fibroblasts, lymphocytes, and tissues using high-performance liquid chromatography-mass spectrometry as a diagnostic test for Barth syndrome. Anal. Biochem. 387(2), 230-237.
- Millar, M.R., Johnson, G., Wilks, M., Skinner, R., Stoneham, S., Pizer, B., Hemsworth, S., Fogarty, A., Steward, C.G., Gilbert, R. and Hennessy, E.M. (2008) Molecular diagnosis of vascular access device-associated infection in children being treated for cancer or leukaemia. Clin. Microbiol. Infect. 14(3), 213-220.
- Kulik, W., van Lenthe, H., Stet, F.S., Houtkooper, R.H., Kemp, H., Stone, J.E., Steward, C.G., Wanders, R.J. and Vaz, F.M. (2008) Bloodspot assay using HPLC-tandem mass spectrometry for detection of Barth syndrome. Clin. Chem. 54(2), 371-378.
- Marks, D.I., Khattry, N., Cummins, M., Goulden, N., Green, A., Harvey, J., Hunt, L.P., Keen, L., Robinson, S.P., Steward, C.G. and Cornish, J.M. (2006) Haploidentical stem cell transplantation for children with acute leukaemia. Br. J. Haematol. 134(2), 196-201.
- Watzinger, F., Lion, T., Steward, C. (2006) Eurochimerism consortium. The RSD code: proposal for a nomenclature of allelic configurations in STR-PCR-based chimerism testing after allogeneic stem cell transplantation. Leukemia 20(8), 1448-1452.
- Steward, C.G., Jarisch, A. (2005) Haemopoietic stem cell transplantation for genetic disorders. Arch. Dis. Child. 90(12), 1259-1263.