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Alessandro Pecci

Showing results (71-80 of 121) with videos related to

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Haematologica|October 13, 2004
Application of a diagnostic algorithm for inherited thrombocytopenias to 46 consecutive patientsPatrizia Noris, Alessandro Pecci, Filomena Di Bari, et al.
Platelets|November 30, 2016
Platelets from glioblastoma patients promote angiogenesis of tumor endothelial cells and exhibit increased VEGF content and releaseClara Di Vito, Stefania Elena Navone, Giovanni Marfia, et al.
Haematologica|December 22, 2010
Clinical and genetic aspects of Bernard-Soulier syndrome: searching for genotype/phenotype correlationsAnna Savoia, Annalisa Pastore, Daniela De Rocco, et al.
European Journal of Haematology|December 17, 2009
MYH9 related disease: four novel mutations of the tail domain of myosin-9 correlating with a mild clinical phenotypeAlessandro Pecci, Emanuele Panza, Daniela De Rocco, et al.
Haematologica|June 5, 2025
Characterization of a novel <i>FLI1</i> mutation in a family with thrombocytopenia and other congenital malformationsDaniele Ammeti, Serena Barozzi, Alessandro Pecci, et al.
EMBO Molecular Medicine|December 2, 2017
Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostimAlessandro Pecci, Iman Ragab, Valeria Bozzi, et al.
Thrombosis and Haemostasis|December 24, 2003
Effects of the R216Q mutation of GATA-1 on erythropoiesis and megakaryocytopoiesisCarlo L Balduini, Alessandro Pecci, Giuseppe Loffredo, et al.
British Journal of Haematology|October 24, 2018
ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopeniaMichela Faleschini, Federica Melazzini, Caterina Marconi, et al.
Blood Cells, Molecules & Diseases|March 14, 2007
The expression of CXCR4 is down-regulated on the CD34+ cells of patients with myelofibrosis with myeloid metaplasiaVittorio Rosti, Margherita Massa, Alessandro M Vannucchi, et al.
Platelets|March 26, 2015
Megakaryocytic emperipolesis and platelet function abnormalities in five patients with gray platelet syndromeLuigi M Larocca, Paula G Heller, Gianmarco Podda, et al.
Pageof 13

Showing results (71-80 of 121) with videos related to

Sort By:
Pageof 13
Haematologica|October 13, 2004
Application of a diagnostic algorithm for inherited thrombocytopenias to 46 consecutive patientsPatrizia Noris, Alessandro Pecci, Filomena Di Bari, et al.
Platelets|November 30, 2016
Platelets from glioblastoma patients promote angiogenesis of tumor endothelial cells and exhibit increased VEGF content and releaseClara Di Vito, Stefania Elena Navone, Giovanni Marfia, et al.
Haematologica|December 22, 2010
Clinical and genetic aspects of Bernard-Soulier syndrome: searching for genotype/phenotype correlationsAnna Savoia, Annalisa Pastore, Daniela De Rocco, et al.
European Journal of Haematology|December 17, 2009
MYH9 related disease: four novel mutations of the tail domain of myosin-9 correlating with a mild clinical phenotypeAlessandro Pecci, Emanuele Panza, Daniela De Rocco, et al.
Haematologica|June 5, 2025
Characterization of a novel <i>FLI1</i> mutation in a family with thrombocytopenia and other congenital malformationsDaniele Ammeti, Serena Barozzi, Alessandro Pecci, et al.
EMBO Molecular Medicine|December 2, 2017
Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostimAlessandro Pecci, Iman Ragab, Valeria Bozzi, et al.
Thrombosis and Haemostasis|December 24, 2003
Effects of the R216Q mutation of GATA-1 on erythropoiesis and megakaryocytopoiesisCarlo L Balduini, Alessandro Pecci, Giuseppe Loffredo, et al.
British Journal of Haematology|October 24, 2018
ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopeniaMichela Faleschini, Federica Melazzini, Caterina Marconi, et al.
Blood Cells, Molecules & Diseases|March 14, 2007
The expression of CXCR4 is down-regulated on the CD34+ cells of patients with myelofibrosis with myeloid metaplasiaVittorio Rosti, Margherita Massa, Alessandro M Vannucchi, et al.
Platelets|March 26, 2015
Megakaryocytic emperipolesis and platelet function abnormalities in five patients with gray platelet syndromeLuigi M Larocca, Paula G Heller, Gianmarco Podda, et al.
Pageof 13