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1. 5'UTR point substitutions and N-terminal truncating mutations of ANKRD26 in acute myeloid leukemia. Issue 1 (December 2017)

2. Mutations of RUNX1 in families with inherited thrombocytopenia. Issue 6 (24th March 2017)

3. The role of an accurate diagnosis of inherited thrombocytopenia as the basis for an effective treatment. A case of MYH9 syndrome treated with a TPO‐RA. Issue 4 (17th April 2019)

4. Megakaryocytic emperipolesis and platelet function abnormalities in five patients with gray platelet syndrome. (17th November 2015)

5. Nonmuscle Myosin Heavy Chain IIA Mutation Predicts Severity and Progression of Sensorineural Hearing Loss in Patients With MYH9-Related Disease. Issue 1 (January 2016)

7. Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC. (16th December 2019)

10. The EHA Research Roadmap: Platelet Disorders. Issue 7 (30th July 2021)