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Silverio Perrotta

Showing results (151-160 of 200) with videos related to

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Orphanet Journal of Rare Diseases|November 26, 2025
Cerebrovascular involvement in hereditary spherocytosis: observational cohort and case-control MRI studyRenzo Manara, Marcella Contieri, Giovanni Librizzi, et al.
American Journal of Hematology|March 22, 2020
White matter volume changes in adult beta-thalassemia: Negligible and unrelated to anemia and cognitive performancesRenzo Manara, Antonietta Canna, Martina Caiazza, et al.
Blood Transfusion = Trasfusione Del Sangue|May 15, 2018
Second-line therapy in paediatric warm autoimmune haemolytic anaemia. Guidelines from the Associazione Italiana Onco-Ematologia Pediatrica (AIEOP)Saverio Ladogana, Matteo Maruzzi, Piera Samperi, et al.
Blood Advances|August 28, 2025
Efficacy and safety of luspatercept in non-transfusion-dependent β-thalassemia: long-term results from the BEYOND studyAli T Taher, Vip Viprakasit, Antonis Kattamis, et al.
Blood|August 25, 2005
The N-terminal 11 amino acids of human erythrocyte band 3 are critical for aldolase binding and protein phosphorylation: implications for band 3 functionSilverio Perrotta, Adriana Borriello, Andrea Scaloni, et al.
Blood Cells, Molecules & Diseases|January 10, 2020
Headache in beta-thalassemia: An Italian multicenter clinical, conventional MRI and MR-angiography case-control studyImmacolata Tartaglione, Martina Caiazza, Rosanna Di Concilio, et al.
Hemasphere|February 9, 2026
Additive effect of multiple genetic variants in <i>SEC23B</i> and <i>PIEZO1</i> on iron metabolism dyshomeostasis in hereditary anemiasAntonella Nostroso, Roberta Marra, Barbara Eleni Rosato, et al.
Haematologica|March 3, 2022
Tricuspid-valve regurgitant jet velocity as a risk factor for death in β-thalassemiaGiorgio Derchi, Khaled M Musallam, Valeria Maria Pinto, et al.
Pediatric Blood & Cancer|September 5, 2017
Hydroxyurea prescription, availability and use for children with sickle cell disease in Italy: Results of a National Multicenter surveyRaffaella Colombatti, Giovanni Palazzi, Nicoletta Masera, et al.
European Journal of Haematology|July 29, 2010
Frequency of congenital dyserythropoietic anemias in EuropeHermann Heimpel, Andreas Matuschek, Momin Ahmed, et al.
Pageof 20

Showing results (151-160 of 200) with videos related to

Sort By:
Pageof 20
Orphanet Journal of Rare Diseases|November 26, 2025
Cerebrovascular involvement in hereditary spherocytosis: observational cohort and case-control MRI studyRenzo Manara, Marcella Contieri, Giovanni Librizzi, et al.
American Journal of Hematology|March 22, 2020
White matter volume changes in adult beta-thalassemia: Negligible and unrelated to anemia and cognitive performancesRenzo Manara, Antonietta Canna, Martina Caiazza, et al.
Blood Transfusion = Trasfusione Del Sangue|May 15, 2018
Second-line therapy in paediatric warm autoimmune haemolytic anaemia. Guidelines from the Associazione Italiana Onco-Ematologia Pediatrica (AIEOP)Saverio Ladogana, Matteo Maruzzi, Piera Samperi, et al.
Blood Advances|August 28, 2025
Efficacy and safety of luspatercept in non-transfusion-dependent β-thalassemia: long-term results from the BEYOND studyAli T Taher, Vip Viprakasit, Antonis Kattamis, et al.
Blood|August 25, 2005
The N-terminal 11 amino acids of human erythrocyte band 3 are critical for aldolase binding and protein phosphorylation: implications for band 3 functionSilverio Perrotta, Adriana Borriello, Andrea Scaloni, et al.
Blood Cells, Molecules & Diseases|January 10, 2020
Headache in beta-thalassemia: An Italian multicenter clinical, conventional MRI and MR-angiography case-control studyImmacolata Tartaglione, Martina Caiazza, Rosanna Di Concilio, et al.
Hemasphere|February 9, 2026
Additive effect of multiple genetic variants in <i>SEC23B</i> and <i>PIEZO1</i> on iron metabolism dyshomeostasis in hereditary anemiasAntonella Nostroso, Roberta Marra, Barbara Eleni Rosato, et al.
Haematologica|March 3, 2022
Tricuspid-valve regurgitant jet velocity as a risk factor for death in β-thalassemiaGiorgio Derchi, Khaled M Musallam, Valeria Maria Pinto, et al.
Pediatric Blood & Cancer|September 5, 2017
Hydroxyurea prescription, availability and use for children with sickle cell disease in Italy: Results of a National Multicenter surveyRaffaella Colombatti, Giovanni Palazzi, Nicoletta Masera, et al.
European Journal of Haematology|July 29, 2010
Frequency of congenital dyserythropoietic anemias in EuropeHermann Heimpel, Andreas Matuschek, Momin Ahmed, et al.
Pageof 20