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Maddalena Casale

Showing results (1-10 of 61) with videos related to

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Expert Review of Hematology|November 15, 2011
Splenectomy for hereditary spherocytosis: complete, partial or not at all?Maddalena Casale, Silverio Perrotta
Italian Journal of Pediatrics|July 30, 2021
Disease burden and quality of life of in children with sickle cell disease in Italy: time to be considered a priorityRaffaella Colombatti, Maddalena Casale, Giovanna Russo
BMJ Case Reports|October 23, 2014
Subarachnoid haemorrhage and cerebral vasculopathy in a child with sickle cell anaemiaBaba Inusa, Maddalena Casale, Caroline Booth, et al.
Plos One|December 4, 2018
Iron chelating properties of Eltrombopag: Investigating its role in thalassemia-induced osteoporosisFrancesca Punzo, Chiara Tortora, Maura Argenziano, et al.
Blood Transfusion = Trasfusione Del Sangue|July 24, 2018
Predicting factors for liver iron overload at the first magnetic resonance in children with thalassaemia majorMaddalena Casale, Maria Marsella, Massimiliano Ammirabile, et al.
Frontiers in Genetics|December 8, 2018
A Novel 12q13.2-q13.3 Microdeletion Syndrome With Combined Features of Diamond Blackfan Anemia, Pierre Robin Sequence and Klippel Feil DeformityDomenico Roberti, Renata Conforti, Teresa Giugliano, et al.
Orphanet Journal of Rare Diseases|October 22, 2013
Organizing national responses for rare blood disorders: the Italian experience with sickle cell disease in childhoodRaffaella Colombatti, Silverio Perrotta, Piera Samperi, et al.
Hemoglobin|September 26, 2018
Life-Threatening Drug-Induced Liver Injury in a Patient with β-Thalassemia Major and Severe Iron Overload on PolypharmacyMaddalena Casale, Stefania Picariello, Felice Corvino, et al.
European Journal of Pediatrics|January 28, 2025
Screening for sickle cell disease by point-of-care tests in Italy: pilot study on 1000 at risk childrenMaddalena Casale, Saverio Scianguetta, Teresa Palma, et al.
Annals of Hematology|July 22, 2020
Manual erythroexchange in sickle cell disease: multicenter validation of a protocol predictive of volume to exchange and hemoglobin valuesBarbara Gianesin, Valeria Maria Pinto, Maddalena Casale, et al.
Pageof 7

Showing results (1-10 of 61) with videos related to

Sort By:
Pageof 7
Expert Review of Hematology|November 15, 2011
Splenectomy for hereditary spherocytosis: complete, partial or not at all?Maddalena Casale, Silverio Perrotta
Italian Journal of Pediatrics|July 30, 2021
Disease burden and quality of life of in children with sickle cell disease in Italy: time to be considered a priorityRaffaella Colombatti, Maddalena Casale, Giovanna Russo
BMJ Case Reports|October 23, 2014
Subarachnoid haemorrhage and cerebral vasculopathy in a child with sickle cell anaemiaBaba Inusa, Maddalena Casale, Caroline Booth, et al.
Plos One|December 4, 2018
Iron chelating properties of Eltrombopag: Investigating its role in thalassemia-induced osteoporosisFrancesca Punzo, Chiara Tortora, Maura Argenziano, et al.
Blood Transfusion = Trasfusione Del Sangue|July 24, 2018
Predicting factors for liver iron overload at the first magnetic resonance in children with thalassaemia majorMaddalena Casale, Maria Marsella, Massimiliano Ammirabile, et al.
Frontiers in Genetics|December 8, 2018
A Novel 12q13.2-q13.3 Microdeletion Syndrome With Combined Features of Diamond Blackfan Anemia, Pierre Robin Sequence and Klippel Feil DeformityDomenico Roberti, Renata Conforti, Teresa Giugliano, et al.
Orphanet Journal of Rare Diseases|October 22, 2013
Organizing national responses for rare blood disorders: the Italian experience with sickle cell disease in childhoodRaffaella Colombatti, Silverio Perrotta, Piera Samperi, et al.
Hemoglobin|September 26, 2018
Life-Threatening Drug-Induced Liver Injury in a Patient with β-Thalassemia Major and Severe Iron Overload on PolypharmacyMaddalena Casale, Stefania Picariello, Felice Corvino, et al.
European Journal of Pediatrics|January 28, 2025
Screening for sickle cell disease by point-of-care tests in Italy: pilot study on 1000 at risk childrenMaddalena Casale, Saverio Scianguetta, Teresa Palma, et al.
Annals of Hematology|July 22, 2020
Manual erythroexchange in sickle cell disease: multicenter validation of a protocol predictive of volume to exchange and hemoglobin valuesBarbara Gianesin, Valeria Maria Pinto, Maddalena Casale, et al.
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