Zobrazeno 1 - 10
of 535
pro vyhledávání: '"G H Hill"'
Autor:
Chris Millar, N. Gill, N. Connor, James W. Ironside, Jonathan T. Wilde, G. Dolan, Mark Winter, Michael Makris, Christine A. Lee, F. G. H. Hill
Publikováno v:
Haemophilia. 16:305-315
Summary. The appearance and rapid evolution ofBSE in UK cattle in the mid 1980s, with compel-ling data supporting variant Creutzfeldt–Jakobdisease (vCJD) as its human manifestation, pose apotentially severe threat to public health. Threeclinical ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b3babb5d3005211844d8ea44b91a486
https://doi.org/10.1111/j.1365-2516.2010.02220.x
https://doi.org/10.1111/j.1365-2516.2010.02220.x
Publikováno v:
British Journal of Haematology. 111:78-90
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bed26ad2090c88c2c7e99f70c5c90fb
https://doi.org/10.1046/j.1365-2141.2000.02327.x
https://doi.org/10.1046/j.1365-2141.2000.02327.x
Autor:
Kate A. Wheeler, Susan M. Richards, Clifford C. Bailey, Brenda Gibson, Ian M. Hann, Frank G. H. Hill, Judith M. Chessells
Publikováno v:
Blood. 96:2412-2418
The role of bone marrow transplantation (BMT) in first remission of children with high-risk acute lymphoblastic leukemia (ALL) remains unclear. There were 3676 patients (aged 1 to 15 years) entered into the United Kingdom (UK) Medical Research Counci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d67b7f86dcc02085f3216e7da0a298a0
https://doi.org/10.1182/blood.v96.7.2412.h8002412_2412_2418
https://doi.org/10.1182/blood.v96.7.2412.h8002412_2412_2418
Publikováno v:
British Journal of Haematology. 89:908-910
Reports of all the factor VIII inhibitors arising in the United Kingdom in patients with haemophilia A during the years 1990-93 have been collated by the United Kingdom Haemophilia Centre Directors Organization. 32 new inhibitors were reported during
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2703612fe30e8c6c92a32677995108a6
https://doi.org/10.1111/j.1365-2141.1995.tb08435.x
https://doi.org/10.1111/j.1365-2141.1995.tb08435.x
Autor:
Ian R. Peake, B. T. Colvin, F. E. Preston, E. P. Mauser Bunschoten, Charles R. M. Hay, F. G. H. Hill, R. Bagnall, N. Wasseem, Karin Fijnvandraat, G. White, E. Santagostino, C. A. Ludlam, Erik Berntorp, Carol K. Kasper
Publikováno v:
Thrombosis and Haemostasis. 79:762-766
SummaryTwenty six patients with mild or moderate haemophilia A and inhibitors are described. The inhibitor was detected at a median age of 33 years, after a median of 5.5 bleeding episodes. This usually following intensive replacement therapy. The me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c35e76f2941a71b96fa72ca28ce91591
https://doi.org/10.1055/s-0037-1615061
https://doi.org/10.1055/s-0037-1615061
Publikováno v:
Haemophilia. 2:244-249
Summary. Chemical mismatch detection has been used to screen selectively part of the A2 domain of exon 28 of the von Willebrand factor gene of three unrelated patients with apparently sporadic type 2A von Willebrand disease (vWD) and their parents an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a746aaaec12248478724cf34f531049
https://doi.org/10.1111/j.1365-2516.1996.tb00145.x
https://doi.org/10.1111/j.1365-2516.1996.tb00145.x
Publikováno v:
Blood Coagulation & Fibrinolysis. 7:134-138
A strategy is described for the initial detection, management and elimination of factor VIII inhibitors arising in patients with congenital and acquired haemophilia A. It is suggested that children with severe haemophilia A should be screened every 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5c17968e6f03f83a9dbc70f43205956
https://doi.org/10.1097/00001721-199603000-00005
https://doi.org/10.1097/00001721-199603000-00005
Autor:
S M A, Zaman, F G H, Hill, B, Palmer, C M, Millar, A, Bone, A M, Molesworth, N, Connor, C A, Lee, G, Dolan, J T, Wilde, O N, Gill, M, Makris
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 17(6)
The risk of variant Creutzfeldt-Jakob disease (vCJD) from potentially infected plasma products remains unquantified. This risk has been assessed for 787 UK patients with an inherited bleeding disorder prospectively followed-up for 10-20 years through
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::58caf53d42fa822f15ba8fdff5c6835c
https://pubmed.ncbi.nlm.nih.gov/21342369
https://pubmed.ncbi.nlm.nih.gov/21342369
Autor:
A, Tosetto, F, Rodeghiero, G, Castaman, A, Goodeve, A B, Federici, J, Batlle, D, Meyer, J, Goudemand, J, Eikenboom, R, Schneppenheim, U, Budde, J, Ingerslev, S, Lethagen, F G H, Hill, I, Peake
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 17(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::62188cfe590d2f1817ae3cf05690e3eb
https://pubmed.ncbi.nlm.nih.gov/21199188
https://pubmed.ncbi.nlm.nih.gov/21199188