Items where authors include "Cartwright, A."

Article

Shepherd, L. orcid.org/0000-0003-0205-6596, Sirois, F.M. orcid.org/0000-0002-0927-277X, Harcourt, D. et al. (7 more authors) (2025) A multi‐centre prospective cohort study investigating the roles of psychological flexibility and self‐compassion in appearance concerns after burn injuries. British Journal of Health Psychology, 30 (1). e12754. ISSN 1359-107X

Scott, S. orcid.org/0000-0001-8182-3057, Devonshire, A. orcid.org/0000-0003-4960-5468, Dillon, R. orcid.org/0000-0001-9333-5296 et al. (16 more authors) (2024) Recommendations from the AML molecular MRD expert advisory board. Leukemia, 38. pp. 1638-1641. ISSN 0887-6924

Shepherd, W. orcid.org/0000-0003-4434-9442, Mounce, S., Gaffney, J. et al. (5 more authors) (2023) Cloud-based artificial Iintelligence analytics to assess combined sewer overflow performance. Journal of Water Resources Planning and Management, 149 (10). 04023051. ISSN 0733-9496

Cartwright, A., Snowden, J.A. orcid.org/0000-0001-6819-3476, Whitehouse, H. et al. (2 more authors) (2023) Implementation of the updated NICE haematological cancers (NG47) improving outcomes guidelines across Specialist Integrated Haematological Malignancy Diagnostic Services (SIHMDS) in England : a UK NEQAS LI survey. Journal of Clinical Pathology, 76 (9). pp. 618-623. ISSN 0021-9746

Scott, S., Cartwright, A., Francis, S. et al. (23 more authors) (2021) Assessment of droplet digital polymerase chain reaction for measuring BCR-ABL1 in chronic myeloid leukaemia in an international interlaboratory study. British Journal of Haematology, 194 (1). pp. 53-60. ISSN 0007-1048

Cartwright, A., Smith, K. and Balasubramanian, M. orcid.org/0000-0003-1488-3695 (2017) Short case report: Xq23 deletion involving PAK3 as a novel cause of developmental delay in a 6-year-old boy. Clinical Dysmorphology, 26 (1). pp. 38-40. ISSN 0962-8827

Cartwright, A., Peake, I.R., Goodeve, A.C. et al. (1 more author) (2016) In silico analysis highlights the copy number variation mechanism responsible for the historically reported VWF exon 42 deletion. Haemophilia. ISSN 1351-8216

Hampshire, D.J. orcid.org/0000-0002-1387-8926, Abuzenadah, A.M., Cartwright, A. et al. (10 more authors) (2013) Identification and characterisation of mutations associated with von Willebrand disease in a Turkish patient cohort. Thrombosis and Haemostasis, 110 (2). pp. 264-274. ISSN 0340-6245