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Maria Lombardi

Showing results (11-20 of 108) with videos related to

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Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|February 26, 2004
A new mutation (Arg251Trp) in the Ca2+ binding site of factor X protease domain appears to be responsible for the defect in the extrinsic pathway activation of factor X PaduaAntonio Girolami, Fabrizio Vianello, Laura Cabrio, et al.
Frontiers in Psychology|June 27, 2017
A Novel Computer-Based Set-Up to Study Movement Coordination in Human EnsemblesFrancesco Alderisio, Maria Lombardi, Gianfranco Fiore, et al.
Hematology (Amsterdam, Netherlands)|September 18, 2012
Recombinant FVIIa concentrate-associated thrombotic events in congenital bleeding disorders other than hemophiliasAntonio Girolami, Giulia Berti de Marinis, Emanuela Bonamigo, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|September 3, 2015
Acquired Isolated FVII Deficiency: An Underestimated and Potentially Important Laboratory FindingAntonio Girolami, Claudia Santarossa, Elisabetta Cosi, et al.
Cureus|December 31, 2019
Ampullary Adenocarcinoma with Incidental Pancreatic Neuroendocrine Tumor: Report of an Extremely Rare Case and Review of LiteratureMatteo Viti, Pietro Maria Lombardi, Mattia Marinelli, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|March 14, 2012
Considerations on a tentative classification of FVII deficiency suited for practical clinical purposesAntonio Girolami, Martina Treleani, Pamela Scarparo, et al.
Frontiers in Robotics and AI|March 24, 2022
Toward an Attentive Robotic Architecture: Learning-Based Mutual Gaze Estimation in Human-Robot InteractionMaria Lombardi, Elisa Maiettini, Davide De Tommaso, et al.
Hematology (Amsterdam, Netherlands)|June 4, 2009
The clinical and laboratory significance of cases of congenital FX deficiency due to defects in the Gla-domainAntonio Girolami, Emanuele Allemand, Raffaella Scandellari, et al.
Journal of Thrombosis and Thrombolysis|May 5, 2009
The clinical significance of the lack of arterial or venous thrombosis in patients with congenital prothrombin or FX deficiencyAntonio Girolami, Nicole Candeo, Silvia Vettore, et al.
Hematology (Amsterdam, Netherlands)|February 9, 2017
Bleeding manifestations in heterozygotes with congenital FVII deficiency: a comparison with unaffected family members during a long observation periodAntonio Girolami, Elisabetta Cosi, Silvia Ferrari, et al.
Pageof 11

Showing results (11-20 of 108) with videos related to

Sort By:
Pageof 11
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|February 26, 2004
A new mutation (Arg251Trp) in the Ca2+ binding site of factor X protease domain appears to be responsible for the defect in the extrinsic pathway activation of factor X PaduaAntonio Girolami, Fabrizio Vianello, Laura Cabrio, et al.
Frontiers in Psychology|June 27, 2017
A Novel Computer-Based Set-Up to Study Movement Coordination in Human EnsemblesFrancesco Alderisio, Maria Lombardi, Gianfranco Fiore, et al.
Hematology (Amsterdam, Netherlands)|September 18, 2012
Recombinant FVIIa concentrate-associated thrombotic events in congenital bleeding disorders other than hemophiliasAntonio Girolami, Giulia Berti de Marinis, Emanuela Bonamigo, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|September 3, 2015
Acquired Isolated FVII Deficiency: An Underestimated and Potentially Important Laboratory FindingAntonio Girolami, Claudia Santarossa, Elisabetta Cosi, et al.
Cureus|December 31, 2019
Ampullary Adenocarcinoma with Incidental Pancreatic Neuroendocrine Tumor: Report of an Extremely Rare Case and Review of LiteratureMatteo Viti, Pietro Maria Lombardi, Mattia Marinelli, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|March 14, 2012
Considerations on a tentative classification of FVII deficiency suited for practical clinical purposesAntonio Girolami, Martina Treleani, Pamela Scarparo, et al.
Frontiers in Robotics and AI|March 24, 2022
Toward an Attentive Robotic Architecture: Learning-Based Mutual Gaze Estimation in Human-Robot InteractionMaria Lombardi, Elisa Maiettini, Davide De Tommaso, et al.
Hematology (Amsterdam, Netherlands)|June 4, 2009
The clinical and laboratory significance of cases of congenital FX deficiency due to defects in the Gla-domainAntonio Girolami, Emanuele Allemand, Raffaella Scandellari, et al.
Journal of Thrombosis and Thrombolysis|May 5, 2009
The clinical significance of the lack of arterial or venous thrombosis in patients with congenital prothrombin or FX deficiencyAntonio Girolami, Nicole Candeo, Silvia Vettore, et al.
Hematology (Amsterdam, Netherlands)|February 9, 2017
Bleeding manifestations in heterozygotes with congenital FVII deficiency: a comparison with unaffected family members during a long observation periodAntonio Girolami, Elisabetta Cosi, Silvia Ferrari, et al.
Pageof 11