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Alessandro Pecci

Showing results (91-100 of 121) with videos related to

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Haematologica|December 15, 2022
Exome sequencing in 116 patients with inherited thrombocytopenia that remained of unknown origin after systematic phenotype-driven diagnostic workupCaterina Marconi, Alessandro Pecci, Flavia Palombo, et al.
Blood|November 2, 2014
ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterizationRoberta Bottega, Caterina Marconi, Michela Faleschini, et al.
Journal of Thrombosis and Haemostasis : JTH|November 22, 2019
Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSCPaolo Gresele, Sara Orsini, Patrizia Noris, et al.
Thrombosis Research|March 13, 2021
Sex differences in Lemierre syndrome: Individual patient-level analysisLuca Valerio, Gabriele Corsi, Serena Granziera, et al.
Hamostaseologie|August 3, 2018
Lemierre Syndrome: Clinical Update and Protocol for a Systematic Review and Individual Patient Data Meta-analysisClara Sacco, Federica Zane, Serena Granziera, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|March 22, 2024
Bioprinting Soft 3D Models of Hematopoiesis using Natural Silk Fibroin-Based Bioink Efficiently Supports Platelet DifferentiationChristian Andrea Di Buduo, Marco Lunghi, Volodymyr Kuzmenko, et al.
British Journal of Haematology|April 27, 2013
Platelet size for distinguishing between inherited thrombocytopenias and immune thrombocytopenia: a multicentric, real life studyPatrizia Noris, Catherine Klersy, Paolo Gresele, et al.
British Journal of Haematology|May 30, 2024
Thrombocytopenia 4 (THC4): Six novel families with mutations of the cytochrome c geneAntonio Marzollo, Stefania Zampieri, Serena Barozzi, et al.
Elife|June 1, 2021
Miniaturized 3D bone marrow tissue model to assess response to Thrombopoietin-receptor agonists in patientsChristian A Di Buduo, Pierre-Alexandre Laurent, Carlo Zaninetti, et al.
Blood|December 29, 2018
Loss-of-function mutations in <i>PTPRJ</i> cause a new form of inherited thrombocytopeniaCaterina Marconi, Christian A Di Buduo, Kellie LeVine, et al.
Pageof 13

Showing results (91-100 of 121) with videos related to

Sort By:
Pageof 13
Haematologica|December 15, 2022
Exome sequencing in 116 patients with inherited thrombocytopenia that remained of unknown origin after systematic phenotype-driven diagnostic workupCaterina Marconi, Alessandro Pecci, Flavia Palombo, et al.
Blood|November 2, 2014
ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterizationRoberta Bottega, Caterina Marconi, Michela Faleschini, et al.
Journal of Thrombosis and Haemostasis : JTH|November 22, 2019
Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSCPaolo Gresele, Sara Orsini, Patrizia Noris, et al.
Thrombosis Research|March 13, 2021
Sex differences in Lemierre syndrome: Individual patient-level analysisLuca Valerio, Gabriele Corsi, Serena Granziera, et al.
Hamostaseologie|August 3, 2018
Lemierre Syndrome: Clinical Update and Protocol for a Systematic Review and Individual Patient Data Meta-analysisClara Sacco, Federica Zane, Serena Granziera, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|March 22, 2024
Bioprinting Soft 3D Models of Hematopoiesis using Natural Silk Fibroin-Based Bioink Efficiently Supports Platelet DifferentiationChristian Andrea Di Buduo, Marco Lunghi, Volodymyr Kuzmenko, et al.
British Journal of Haematology|April 27, 2013
Platelet size for distinguishing between inherited thrombocytopenias and immune thrombocytopenia: a multicentric, real life studyPatrizia Noris, Catherine Klersy, Paolo Gresele, et al.
British Journal of Haematology|May 30, 2024
Thrombocytopenia 4 (THC4): Six novel families with mutations of the cytochrome c geneAntonio Marzollo, Stefania Zampieri, Serena Barozzi, et al.
Elife|June 1, 2021
Miniaturized 3D bone marrow tissue model to assess response to Thrombopoietin-receptor agonists in patientsChristian A Di Buduo, Pierre-Alexandre Laurent, Carlo Zaninetti, et al.
Blood|December 29, 2018
Loss-of-function mutations in <i>PTPRJ</i> cause a new form of inherited thrombocytopeniaCaterina Marconi, Christian A Di Buduo, Kellie LeVine, et al.
Pageof 13