Zobrazeno 1 - 10 of 50 pro vyhledávání: '"G H Hill"'
1
Cytolytic activity against mycobacterial antigens: differences between haemophiliacs with and without HIV infection
Autor: J. A. Evans, D. S. Kumararatne, K. J. Pasi, F. G. H. Hill, M. Forte
Publikováno v: Haemophilia : the official journal of the World Federation of Hemophilia. 1(3)
Although asymptomatic haemophiliacs have been shown to have abnormalities of their immune response, independent of HIV, clinical evidence of significant immunosuppression is limited. The only clinical report has been an outbreak of M. tuberculosis in
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51f52ede3d464e505163dbbb663449d7
https://pubmed.ncbi.nlm.nih.gov/27214536
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2
Risk reduction strategies for variant Creutzfeldt-Jakob disease transmission by UK plasma products and their impact on patients with inherited bleeding disorders
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
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5
Bone marrow transplantation versus chemotherapy in the treatment of very high–risk childhood acute lymphoblastic leukemia in first remission: results from Medical Research Council UKALL X and XI
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
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6
The incidence of factor VIII inhibitors in the United Kingdom, 1990-93
Autor: F. G. H. Hill, C. R. M. Hay, F. E. Preston, B. T. Colvin
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
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7
Factor VIII Inhibitors in Mild and Moderate-severity Haemophilia A
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
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8
De novo mutation causing sporadic type 2A von Willebrancd's disease: report of three cases
Autor: F. G. H. Hill, M. S. Enayat, B. D. M. Theophilus, K. J. Pasi
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
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9
Recommendations for the treatment of factor VIII inhibitors
Autor: F. E. Preston, Christopher A. Ludlam, Charles R. M. Hay, B. T. Colvin, F. G. H. Hill
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
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10
The risk of variant Creutzfeldt-Jakob disease among UK patients with bleeding disorders, known to have received potentially contaminated plasma products
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
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