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3. A synonymous (c.3390C>T) or a splice‐site (c.3380‐2A>G) mutation causes exon 26 skipping in four patients with von Willebrand disease (2A/IIE). Issue 7 (15th July 2013)

6. Evaluation of an heterogeneous group of patients with von Willebrand disease using an assay alternative to ristocetin induced platelet agglutination. (27th August 2015)

7. Predictors of von Willebrand disease diagnosis in individuals with borderline von Willebrand factor plasma levels. (9th January 2015)