Publications by authors named "Said Enayat"

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A novel D235Y mutation in the GP1BA gene enhances platelet interaction with von Willebrand factor in an Iranian family with platelet-type von Willebrand disease.
Said Enayat, Shirin Ravanbod, Maryam Rassoulzadegan, Mohammad Jazebi, Shirin Tarighat

Thromb Haemost· November 2012

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Frequency of platelet type versus type 2B von Willebrand disease. An international registry-based study.
Alexander Hamilton, Margareth Ozelo, Jayne Leggo, Colleen Notley, Hannah Brown, Said M Enayat

Thromb Haemost· March 2011

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Is VWF R924Q a benign polymorphism, a marker of a null allele or a factor VIII-binding defect? The debate continues with results from the UKHCDO VWD study.
William Lester, Andrea Guilliatt, Pamela Grundy, Said Enayat, Carolyn Millar

Thromb Haemost· October 2008

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The R2464C missense mutation in the von Willebrand factor gene causes a novel abnormality of multimer electrophoretic mobility and falls into the subgroup of type 2 von Willebrand disease 'unclassified'.
William A Lester, Andrea M Guilliatt, M Said Enayat, Peter Rose, Frank G H Hill

Thromb Haemost· January 2007

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An investigation of the von Willebrand factor genotype in UK patients diagnosed to have type 1 von Willebrand disease.
Anthony Cumming, Pamela Grundy, Stephen Keeney, William Lester, Said Enayat

Thromb Haemost· November 2006

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Inherited and de novo von Willebrand disease 'Vicenza' in UK families with the R1205H mutation: diagnostic pitfalls and new insights.
William A Lester, Andrea M Guilliatt, Gurcharan K Surdhar, Said M Enayat, Jonathan T Wilde

Br J Haematol· October 2006

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Successful treatment of congenital thrombotic thrombocytopenic purpura using the intermediate purity factor VIII concentrate BPL 8Y.
Will A Lester, Michael D Williams, Sarah L Allford, M Said Enayat, Samuel J Machin

Br J Haematol· October 2002

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