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Dominant inheritance of a novel integrin beta3 mutation associated with a hereditary macrothrombocytopenia and platelet dysfunction in two Italian families.
Gresele P, Falcinelli E, Giannini S, D'Adamo P, D'Eustacchio A, Corazzi T, Mezzasoma AM, Di Bari F, Guglielmini G, Cecchetti L, Noris P, Balduini CL, Savoia A. Gresele P, et al. Haematologica. 2009 May;94(5):663-9. doi: 10.3324/haematol.2008.002246. Epub 2009 Mar 31. Haematologica. 2009. PMID: 19336737 Free PMC article.
Matrix metalloproteinases and peripheral arterial disease.
Busti C, Falcinelli E, Momi S, Gresele P. Busti C, et al. Among authors: gresele p. Intern Emerg Med. 2010 Feb;5(1):13-25. doi: 10.1007/s11739-009-0283-y. Epub 2009 Jul 21. Intern Emerg Med. 2010. PMID: 19626421 Review.
Diagnosis of platelet-type von Willebrand disease by flow cytometry.
Giannini S, Cecchetti L, Mezzasoma AM, Gresele P. Giannini S, et al. Among authors: gresele p. Haematologica. 2010 Jun;95(6):1021-4. doi: 10.3324/haematol.2009.015990. Epub 2009 Nov 30. Haematologica. 2010. PMID: 19951970 Free PMC article.
379 results