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Alessia Marcon

Showing results (1-10 of 15) with videos related to

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Hemasphere|June 7, 2021
Innovative Treatments for Rare AnemiasMaria Domenica Cappellini, Alessia Marcon, Bruno Fattizzo, et al.
Hematology/Oncology Clinics of North America|February 21, 2018
Clinical Complications and Their ManagementAlessia Marcon, Irene Motta, Ali T Taher, et al.
Mediterranean Journal of Hematology and Infectious Diseases|March 19, 2011
Coagulopathy in Beta-thalassemia: current understanding and future perspectivesM Domenica Cappellini, Khaled M Musallam, Alessia Marcon, et al.
Expert Review of Hematology|October 30, 2019
Management of age-associated medical complications in patients with β-thalassemiaIrene Motta, Marta Mancarella, Alessia Marcon, et al.
Annals of Hematology|September 17, 2021
Epidemiological shift of glucose-6-phosphate dehydrogenase mutations in northern Italy in the last 15 yearsLorena Duca, Isabella Nava, Dario Tavazzi, et al.
Journal of Research in Medical Sciences : the Official Journal of Isfahan University of Medical Sciences|April 29, 2011
Pregnant women affected by thalassemia major: a controlled study of traits and personalityGiuseppina Messina, Elisa Colombo, Elena Cassinerio, et al.
Haematologica|August 4, 2009
Hypercoagulability in splenectomized thalassemic patients detected by whole-blood thromboelastometry, but not by thrombin generation in platelet-poor plasmaArmando Tripodi, Maria Domenica Cappellini, Veena Chantarangkul, et al.
Blood Cells, Molecules & Diseases|June 26, 2012
Longitudinal changes in serum ferritin levels correlate with measures of hepatic stiffness in transfusion-independent patients with β-thalassemia intermediaKhaled M Musallam, Irene Motta, Marta Salvatori, et al.
British Journal of Haematology|October 22, 2016
Pulmonary dysfunction in thalassaemia major: is there any relationship with body iron stores?Francesca Guidotti, Gioia Piatti, Alessia Marcon, et al.
Annals of Hematology|June 29, 2010
Endocrine and bone disease in appropriately treated adult patients with beta-thalassemia majorMarina Baldini, Stella Forti, Alessia Marcon, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Hemasphere|June 7, 2021
Innovative Treatments for Rare AnemiasMaria Domenica Cappellini, Alessia Marcon, Bruno Fattizzo, et al.
Hematology/Oncology Clinics of North America|February 21, 2018
Clinical Complications and Their ManagementAlessia Marcon, Irene Motta, Ali T Taher, et al.
Mediterranean Journal of Hematology and Infectious Diseases|March 19, 2011
Coagulopathy in Beta-thalassemia: current understanding and future perspectivesM Domenica Cappellini, Khaled M Musallam, Alessia Marcon, et al.
Expert Review of Hematology|October 30, 2019
Management of age-associated medical complications in patients with β-thalassemiaIrene Motta, Marta Mancarella, Alessia Marcon, et al.
Annals of Hematology|September 17, 2021
Epidemiological shift of glucose-6-phosphate dehydrogenase mutations in northern Italy in the last 15 yearsLorena Duca, Isabella Nava, Dario Tavazzi, et al.
Journal of Research in Medical Sciences : the Official Journal of Isfahan University of Medical Sciences|April 29, 2011
Pregnant women affected by thalassemia major: a controlled study of traits and personalityGiuseppina Messina, Elisa Colombo, Elena Cassinerio, et al.
Haematologica|August 4, 2009
Hypercoagulability in splenectomized thalassemic patients detected by whole-blood thromboelastometry, but not by thrombin generation in platelet-poor plasmaArmando Tripodi, Maria Domenica Cappellini, Veena Chantarangkul, et al.
Blood Cells, Molecules & Diseases|June 26, 2012
Longitudinal changes in serum ferritin levels correlate with measures of hepatic stiffness in transfusion-independent patients with β-thalassemia intermediaKhaled M Musallam, Irene Motta, Marta Salvatori, et al.
British Journal of Haematology|October 22, 2016
Pulmonary dysfunction in thalassaemia major: is there any relationship with body iron stores?Francesca Guidotti, Gioia Piatti, Alessia Marcon, et al.
Annals of Hematology|June 29, 2010
Endocrine and bone disease in appropriately treated adult patients with beta-thalassemia majorMarina Baldini, Stella Forti, Alessia Marcon, et al.
Pageof 2