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Alessandro Pecci

Showing results (41-50 of 121) with videos related to

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Journal of Hematology & Oncology|June 18, 2015
Particulate cytoplasmic structures with high concentration of ubiquitin-proteasome accumulate in myeloid neoplasmsAlessandro Pecci, Vittorio Necchi, Serena Barozzi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 18, 2019
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-RAMarika Porrazzo, Erminia Baldacci, Antonietta Ferretti, et al.
Platelets|June 14, 2006
Unexplained recurrent venous thrombosis in a patient with MYH9-related diseasePaula G Heller, Alessandro Pecci, Ana C Glembotsky, et al.
British Journal of Haematology|April 10, 2024
ACTN1-related thrombocytopenia: Homozygosity for an ACTN1 variant results in a more severe phenotypeMelania Eva Zanchetta, Serena Barozzi, Federica Isidori, et al.
Acta Ophthalmologica|April 8, 2021
Ophthalmic complications of Lemierre syndromeRobert Kreuzpointner, Luca Valerio, Gabriele Corsi, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 20, 2005
Circulating CD34+, CD133+, and vascular endothelial growth factor receptor 2-positive endothelial progenitor cells in myelofibrosis with myeloid metaplasiaMargherita Massa, Vittorio Rosti, Isabella Ramajoli, et al.
Thrombosis and Haemostasis|December 11, 2012
Ubiquitin/proteasome-rich particulate cytoplasmic structures (PaCSs) in the platelets and megakaryocytes of ANKRD26-related thrombo-cytopeniaVittorio Necchi, Alessandra Balduini, Patrizia Noris, et al.
Experimental Cell Research|September 24, 2004
Expression, activation, and subcellular localization of the Rap1 GTPase in cord blood-derived human megakaryocytesAlessandra Balduini, Alessandro Pecci, Paolo Lova, et al.
International Journal of Molecular Medicine|April 6, 2006
Non-muscle myosin heavy chain IIA and IIB interact and co-localize in living cells: relevance for MYH9-related diseaseMonica Marini, Maurizio Bruschi, Alessandro Pecci, et al.
British Journal of Haematology|May 4, 2017
A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin genePatrizia Noris, Caterina Marconi, Daniela De Rocco, et al.
Pageof 13

Showing results (41-50 of 121) with videos related to

Sort By:
Pageof 13
Journal of Hematology & Oncology|June 18, 2015
Particulate cytoplasmic structures with high concentration of ubiquitin-proteasome accumulate in myeloid neoplasmsAlessandro Pecci, Vittorio Necchi, Serena Barozzi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 18, 2019
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-RAMarika Porrazzo, Erminia Baldacci, Antonietta Ferretti, et al.
Platelets|June 14, 2006
Unexplained recurrent venous thrombosis in a patient with MYH9-related diseasePaula G Heller, Alessandro Pecci, Ana C Glembotsky, et al.
British Journal of Haematology|April 10, 2024
ACTN1-related thrombocytopenia: Homozygosity for an ACTN1 variant results in a more severe phenotypeMelania Eva Zanchetta, Serena Barozzi, Federica Isidori, et al.
Acta Ophthalmologica|April 8, 2021
Ophthalmic complications of Lemierre syndromeRobert Kreuzpointner, Luca Valerio, Gabriele Corsi, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 20, 2005
Circulating CD34+, CD133+, and vascular endothelial growth factor receptor 2-positive endothelial progenitor cells in myelofibrosis with myeloid metaplasiaMargherita Massa, Vittorio Rosti, Isabella Ramajoli, et al.
Thrombosis and Haemostasis|December 11, 2012
Ubiquitin/proteasome-rich particulate cytoplasmic structures (PaCSs) in the platelets and megakaryocytes of ANKRD26-related thrombo-cytopeniaVittorio Necchi, Alessandra Balduini, Patrizia Noris, et al.
Experimental Cell Research|September 24, 2004
Expression, activation, and subcellular localization of the Rap1 GTPase in cord blood-derived human megakaryocytesAlessandra Balduini, Alessandro Pecci, Paolo Lova, et al.
International Journal of Molecular Medicine|April 6, 2006
Non-muscle myosin heavy chain IIA and IIB interact and co-localize in living cells: relevance for MYH9-related diseaseMonica Marini, Maurizio Bruschi, Alessandro Pecci, et al.
British Journal of Haematology|May 4, 2017
A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin genePatrizia Noris, Caterina Marconi, Daniela De Rocco, et al.
Pageof 13