Zobrazeno 1 - 10 of 62 pro vyhledávání: '"B. T. Colvin"'
1
Current Practice in the Treatment of Haemophilia
Autor: Mary R. Cahill, B. T. Colvin
Publikováno v: Hematology (Amsterdam, Netherlands). 2(5)
Haematologists are long standing proponents of evidence based practice-well exemplified among professionals who care for patients with haemophilia. The rapidly expanding range of therapeutic products and the numerous accompanying clinical trials are
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b9fce19b19d3c6ef5f4d2e30e9459b4
https://pubmed.ncbi.nlm.nih.gov/27405401
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2
Alpha interferon for hepatitis C virus infection in haemophilic patients
Autor: Sheila Hayden, Paul Telfer, Helen Devereux, Christine Lee, B. T. Colvin, Geoffrey Dusheiko
Publikováno v: Haemophilia : the official journal of the World Federation of Hemophilia. 1(1)
We have conducted a controlled trial in 20 haemophilic patients in which intravenous recombinant interferon alpha-2a, 3 mega units thrice weekly, was used to treat chronic hepatitis C infection. The study endpoints included complete and paritial norm
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9c429522fd5c81d713affd98298ca96
https://pubmed.ncbi.nlm.nih.gov/27214222
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4
European principles of haemophilia care
Autor: Riitta Lassila, Alessandro Gringeri, Jørgen Ingerslev, Angela Thomas, Krista Fischer, Jan Astermark, B. T. Colvin, W. Schramm
Publikováno v: Colvin, B T, Astermark, J, Fischer, K, Gringeri, A, Lassila, R, Schramm, W, Thomas, A, Ingerslev, J & Inter Disciplinary Working Group 2008, ' European principles of haemophilia care ', Haemophilia, vol. 14, no. 2, pp. 361-74 . https://doi.org/10.1111/j.1365-2516.2007.01625.x
Udgivelsesdato: 2008-Mar As the management of haemophilia is complex, it is essential that those with the disorder should have ready access to a range of services provided by a multidisciplinary team of specialists. This document sets out the princip
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea84343f48e123ba2a1494412335e7e2
https://doi.org/10.1111/j.1365-2516.2007.01625.x
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7
Spontaneous intracranial bleeding in two patients with congenital afibrinogenaemia and the role of replacement therapy
Autor: J. P. Dickinson, B. T. Colvin, David Keeling, S. De Lord, R. Parameswaran
Publikováno v: Haemophilia. 6:705-708
Congenital afibrinogenaemia and hypofibrinogenaemia are rare disorders of haemostasis. In this case report the problems posed in the management of two patients with fibrinogen levels less than 0.1g L(-1) and who developed intracranial bleeding are co
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5f718fb8a0b37de103be5ca78deb068b
https://doi.org/10.1046/j.1365-2516.2000.00448.x
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8
Creation of a novel donor splice site in intron 1 of the factor VIII gene leads to activation of a 191 bp cryptic exon in two haemophilia A patients
Autor: Francesco Giannelli, B. T. Colvin, Christine Lee, Peter M. Green, Richard Bagnall, Naushin Waseem
Publikováno v: British Journal of Haematology. 107:766-771
Summary. We have constructed a confidential U.K. database of haemophilia A mutations and pedigrees by characterizing the gene defect of one index patient in each U.K. family. Mutations were identified by screening all coding regions of the factor VII
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ef6b4e4cb4c9fa9cbc98e4f84d0f6114
https://doi.org/10.1046/j.1365-2141.1999.01767.x
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9
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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10
Management of a premature infant with moderate haemophilia A using recombinant factor VIII
Autor: M F Hird, R F Gale, B. T. Colvin
Publikováno v: Haemophilia. 4:850-853
The birth of a very premature infant with haemophilia A is a rare event. In this case report the problems posed in the management of a child with a factor VIII level of 0.03 IU mL-1 born at 28 weeks of gestation and weighing 1590 g are considered. Th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::77d1220ea60496d9e94fcad6ca436f38
https://doi.org/10.1046/j.1365-2516.1998.00201.x
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