Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Philip J Darbyshire"'
Autor:
Ashish Narayan Masurekar, Catriona A Parker, Milensu Shanyinde, Anthony V Moorman, Jeremy P Hancock, Rosemary Sutton, Philip J Ancliff, Mary Morgan, Nicholas J Goulden, Chris Fraser, Peter M Hoogerbrugge, Tamas Revesz, Philip J Darbyshire, Shekhar Krishnan, Sharon B Love, Vaskar Saha
Publikováno v:
PLoS ONE, Vol 9, Iss 10, p e108107 (2014)
The outcomes of Central Nervous System (CNS) relapses in children with acute lymphoblastic leukaemia (ALL) treated in the ALL R3 trial, between January 2003 and March 2011 were analysed. Patients were risk stratified, to receive a matched donor allog
Externí odkaz:
https://doaj.org/article/a33a747b941a4d608fce934190131089
Autor:
Rachel M. Brown, Philip J. Darbyshire, Peter M. Gillett, Madhur Ravikumara, Frank G.H. Hill, Angela Thomas, Patrick J. McKiernan, David C. Wilson
Publikováno v:
Journal of Pediatric Gastroenterology and Nutrition. 42:535-538
6-Thioguanine treatment in childhood acute lymphoblastic leukaemia (ALL) has been shown to cause hepatic veno-occlusive disease, but this usually resolved with drug withdrawal. Recent reports suggested that treatment of ALL with 6-thioguanine can lea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b99f414dba9f658e921ab61952de9797
https://doi.org/10.1097/01.mpg.0000221901.76404.07
https://doi.org/10.1097/01.mpg.0000221901.76404.07
Autor:
Elaine Green, Carmel M. McConville, Judith E. Powell, Jillian R. Mann, Philip J. Darbyshire, A. Malcolm R. Taylor, Tatjana Stankovic
Publikováno v:
Blood. 92:952-958
Current prognostic indicators such as age, sex, and white blood cell count (WBC) fail to identify all children with more aggressive forms of B-precursor acute lymphoblastic leukemia (ALL), and a proportion of patients without poor prognostic indicato
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63cb3cd4e1c45d16f4b4c285c00f3f6e
https://doi.org/10.1182/blood.v92.3.952.415k29_952_958
https://doi.org/10.1182/blood.v92.3.952.415k29_952_958
Bone marrow transplantation for beta-thalassaemia major: the UK experience in two paediatric centres
Autor:
Sarah E, Lawson, Irene A G, Roberts, Persis, Amrolia, Inderjeet, Dokal, Richard, Szydlo, Philip J, Darbyshire
Publikováno v:
British journal of haematology. 120(2)
Stem cell transplantation (SCT) remains the only cure for thalassaemia major. Recent advances in medical treatment make it even more important that accurate information is available regarding outcome of SCT in relevant patient populations in order to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3cc8155d6c75b9fa73bed929cb7bc66c
https://pubmed.ncbi.nlm.nih.gov/12542489
https://pubmed.ncbi.nlm.nih.gov/12542489
Publikováno v:
Cancer Genetics and Cytogenetics. 28:377-378
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a94d5c7119ca89eb03b08e9d7a83747c
https://doi.org/10.1016/0165-4608(87)90229-9
https://doi.org/10.1016/0165-4608(87)90229-9