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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.
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.
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.
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