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Internal and Emergency Medicine|July 29, 2009
Essential thrombocythemia: past and presentFabrizio Fabris, Maria Luigia RandiExpert Opinion on Pharmacotherapy|May 25, 2004
Essential thrombocythaemia in children: is a treatment needed?Maria Luigia Randi, Maria Caterina PuttiCancers|December 10, 2021
Essential Thrombocythemia in Children and AdolescentsMaria Caterina Putti, Irene Bertozzi, Maria Luigia RandiExpert Review of Hematology|March 31, 2019
Contemporary management of essential thrombocythemia in childrenMaria Luigia Randi, Irene Bertozzi, Maria Caterina PuttiJournal of Experimental & Clinical Cancer Research : CR|October 6, 2023
Acute myeloid leukemia: from NGS, through scRNA-seq, to CAR-T. dissect cancer heterogeneity and tailor the treatmentEdoardo Peroni, Maria Luigia Randi, Antonio Rosato, et al.Blood Cells, Molecules & Diseases|March 19, 2019
Heterozygous FXII deficiency is not associated with an increased incidence of thrombotic events: Results of a long term studyAntonio Girolami, Silvia Ferrari, Elisabetta Cosi, et al.Hematology (Amsterdam, Netherlands)|December 4, 2019
New data on FII, FV, FIX and thrombomodulin defects: blood keeps clotting in normal and in peculiar waysAntonio Girolami, Silvia Ferrari, Bruno Girolami, et al.Journal of Thrombosis and Thrombolysis|January 30, 2019
Thrombotic events in severe FXII deficiency in comparison with unaffected family members during a long observation periodAntonio Girolami, Silvia Ferrari, Elisabetta Cosi, et al.Seminars in Thrombosis and Hemostasis|May 15, 2015
The Story of Serum Prothrombin Conversion Accelerator, Proconvertin, Stable Factor, Cothromboplastin, Prothrombin Accelerator or Autoprothrombin I, and Their Subsequent Merging into Factor VIIAntonio Girolami, Elisabetta Cosi, Claudia Santarossa, et al.Seminars in Thrombosis and Hemostasis|April 16, 2015
Complex history of the discovery and characterization of congenital factor X deficiencyAntonio Girolami, Elisabetta Cosi, Luisa Sambado, et al.Pageof 7