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Haemophilia : the Official Journal of the World Federation of Hemophilia|July 10, 2001
Site and type of mutations in the factor VIII gene in patients and carriers of haemophilia AB D Theophilus, M S Enayat, M D Williams, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
De novo mutation causing sporadic type 2A von Willebrancd's disease: report of three casesM S Enayat, B D Theophilus, K J Pasi, et al.Thrombosis and Haemostasis|April 7, 1987
Evaluation of monoclonal antibodies to vWf antigen for use in autoradiographing vWf multimer analysisM S Enayat, F G Hill, W Robinson, et al.Journal of Clinical Pathology|February 1, 1984
Lack of correlation between factor VIII related antigen multimeric analysis pattern and parallel or non-parallel dose response curves in an ELISA factor VIII related antigen assayP E Short, C E Williams, M S Enayat, et al.Thrombosis and Haemostasis|October 6, 2000
A new candidate missense mutation (Leu 1657 IIe) in an apparently asymptomatic type 2A (phenotype IIA) von Willebrand disease familyM S Enayat, A M Guilliatt, G K Surdhar, et al.Thrombosis Research|August 1, 1990
Qualitative and quantitative abnormalities of von Willebrand antigen in patients with diabetes mellitusK J Pasi, M S Enayat, P M Horrocks, et al.Human Mutation|April 24, 1999
Independent occurrence of the novel Arg2163 to His mutation in the factor VIII gene in three unrelated families with haemophila A with different phenotypes. Mutations in brief no. 126. OnlineB D Theophilus, M S Enayat, M Higuchi, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|December 1, 2004
Mutation analysis in F9 gene of 17 families with haemophilia B from IranM S Enayat, M Karimi, G Chana, et al.European Journal of Haematology|September 1, 1989
Vascular endothelial cell function and ultrastructure in thrombotic microangiopathy following allogeneic bone marrow transplantationH Cohen, H A Bull, A Seddon, et al.Thrombosis and Haemostasis|January 12, 2001
Identification of type 2 von Willebrand disease in previously diagnosed type 1 patients: a reappraisal using phenotypes, genotypes and molecular modellingI C Nitu-Whalley, A Riddell, C A Lee, et al.Pageof 3