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Items: 3

1.
Visualizing the von Willebrand factor/glycoprotein Ib-IX axis with a platelet-type von Willebrand disease mutation
Jose A. Guerrero, Mark Kyei, Susan Russell, Junling Liu, T. Kent Gartner, Brian Storrie, Jerry Ware
Blood. 2009 Dec 24; 114(27): 5541–5546. Prepublished online 2009 Oct 6. doi: 10.1182/blood-2009-03-210823
PMCID:
PMC2798865
AbstractArticle
2.
Dominant inheritance of a novel integrin β3 mutation associated with a hereditary macrothrombocytopenia and platelet dysfunction in two Italian families
Paolo Gresele, Emanuela Falcinelli, Silvia Giannini, Pio D’Adamo, Angela D’Eustacchio, Teresa Corazzi, Anna Maria Mezzasoma, Filomena Di Bari, Giuseppe Guglielmini, Luca Cecchetti, Patrizia Noris, Carlo L. Balduini, Anna Savoia
Haematologica. 2009 May; 94(5): 663–669. Published online 2009 Mar 31. doi: 10.3324/haematol.2008.002246
PMCID:
PMC2675678
AbstractArticlePDF–377K
3.
Inherited thrombocytopenia with thrombasthenia
N. K. Sheth, T. A. J. Prankerd
J Clin Pathol. 1968 Mar; 21(2): 154–156. doi: 10.1136/jcp.21.2.154
PMCID:
PMC473712
SummaryPage BrowsePDF–395K

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