Zobrazeno 1 - 4
of 4
pro vyhledávání: '"P J, Ancliff"'
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:
Matt Wenham, Samantha Grieve, Michelle Cummins, Matthew L. Jones, Sarah Booth, Rachel Kilner, Philip J. Ancliff, Gillian M. Griffiths, Andrew D. Mumford
Publikováno v:
Haematologica, Vol 95, Iss 2 (2010)
Hermansky Pudlak syndrome type 2 (HPS2) is a rare disorder associated with mutations in the Adaptor Protein 3 (AP-3) complex, which is involved in sorting transmembrane proteins to lysosomes and related organelles. We now report 2 unrelated subjects
Externí odkaz:
https://doaj.org/article/01897d01ce874b15b3fba6dc3d45174e
Autor:
R. T. Howell, Keith W. Brown, Ruth Newbury-Ecob, P J Ancliff, K. L. Greenhalgh, Ellen G Vernon, C C Verschuuren-Bemelmans, H G Brunner, A. Bottani
Publikováno v:
Journal of Medical Genetics, 39, 876-81
Journal of Medical Genetics, 39, 12, pp. 876-81
JOURNAL OF MEDICAL GENETICS, 39(12), 876-881. BMJ PUBLISHING GROUP
Journal of Medical Genetics, 39, 12, pp. 876-81
JOURNAL OF MEDICAL GENETICS, 39(12), 876-881. BMJ PUBLISHING GROUP
Item does not contain fulltext The thrombocytopenia-absent radius (TAR) syndrome is a congenital malformation syndrome characterised by bilateral absence of the radii and a thrombocytopenia. The lower limbs, gastrointestinal, cardiovascular, and othe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ccdcfee9df51e726797f180082b0e63
http://hdl.handle.net/2066/185509
http://hdl.handle.net/2066/185509
Publikováno v:
Bone marrow transplantation. 13(6)
We describe a case of a 38-year-old female who presented with diarrhoea and abdominal pain 27 days after a second 'top-up' allogeneic marrow infusion for acute myeloid leukaemia (AML) in first remission. A clinical diagnosis of gut graft-versus-host