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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.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.Methods in Molecular Medicine|February 23, 2011
Multimeric analysis of von Willebrand factorM S EnayatJournal of Helminthology|June 1, 1977
The comparison of counterimmunoelectrophoresis with indirect haemagglutination test for detection of antibodies in experimentally infected guinea pigs with Toxocara canisM S Enayat, M PezeshkiMethods in Molecular Medicine|February 23, 2011
Use of Intron 40 VNTR I in vWD Gene TrackingM S Enayat, G K SurdharBlood|July 27, 2001
Aberrant dimerization of von Willebrand factor as the result of mutations in the carboxy-terminal region: identification of 3 mutations in members of 3 different families with type 2A (phenotype IID) von Willebrand diseaseM S Enayat, A M Guilliatt, G K Surdhar, et al.Pediatric Hematology and Oncology|July 1, 1993
Congenital microangiopathic haemolytic anemia: a variant of thrombotic thrombocytopenic purpura?P C Sartori, M S Enayat, P J DarbyshireArchives of Disease in Childhood|September 22, 1999
Congenital thrombophilia and thrombosis: a study in a single centreS E Lawson, D Butler, M S Enayat, et al.Vox Sanguinis|January 1, 1977
Expression of red cell Bga antigen in children. Lack of correlation with previous EB virus infectionJ A Morton, F G HillPageof 7