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Raffaella Mariani

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Haematologica|August 28, 2025
β-thalassemia trait and iron overload: is it time to consider oral iron chelators? Comments on: "A case series of patients with β-thalassemia trait and iron overload: from multifactorial hepcidin suppression to treatment with mini-phlebotomies"Alberto Piperno, Raffaella Mariani
International Journal of Molecular Sciences|February 11, 2023
Hereditary HyperferritinemiaAlberto Piperno, Sara Pelucchi, Raffaella Mariani
Translational Gastroenterology and Hepatology|April 8, 2020
Inherited iron overload disordersAlberto Piperno, Sara Pelucchi, Raffaella Mariani
Mediterranean Journal of Hematology and Infectious Diseases|March 19, 2011
Iron metabolism in thalassemia and sickle cell diseaseRaffaella Mariani, Paola Trombini, Matteo Pozzi, et al.
World Journal of Gastroenterology|February 6, 2009
Hepcidin modulation in human diseases: from research to clinicAlberto Piperno, Raffaella Mariani, Paola Trombini, et al.
European Journal of Case Reports in Internal Medicine|May 6, 2022
Rhabdomyolysis after Intravenous Ferric Gluconate: A Case ReportMara Botti, Alberto Piperno, Annalia Cianflone, et al.
Mediterranean Journal of Hematology and Infectious Diseases|March 22, 2021
Mental Well-Being in Patients with Transfusion-Dependent Anemias and Hemochromatosis during the SARS-CoV-2 PandemicRachele Piperno, Gabriella Bertazioli, Giulia Ravasi, et al.
AJNR. American Journal of Neuroradiology|March 12, 2005
MR imaging of cerebral cortical involvement in aceruloplasminemiaMarina Grisoli, Alberto Piperno, Luisa Chiapparini, et al.
British Journal of Haematology|November 28, 2008
Reduced expression of hepcidin in patients with myelodysplastic syndrome and myelofibrosis: the causes might be more heterogeneous than in thalassaemiaRaffaella Mariani, Sara Pelucchi, Matteo Pozzi, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|May 4, 2020
Ferroportin disease: A novel SLC40A1 mutationGiulia Ravasi, Sara Pelucchi, Andrea Russo, et al.
Pageof 5

Showing results (1-10 of 50) with videos related to

Sort By:
Pageof 5
Haematologica|August 28, 2025
β-thalassemia trait and iron overload: is it time to consider oral iron chelators? Comments on: "A case series of patients with β-thalassemia trait and iron overload: from multifactorial hepcidin suppression to treatment with mini-phlebotomies"Alberto Piperno, Raffaella Mariani
International Journal of Molecular Sciences|February 11, 2023
Hereditary HyperferritinemiaAlberto Piperno, Sara Pelucchi, Raffaella Mariani
Translational Gastroenterology and Hepatology|April 8, 2020
Inherited iron overload disordersAlberto Piperno, Sara Pelucchi, Raffaella Mariani
Mediterranean Journal of Hematology and Infectious Diseases|March 19, 2011
Iron metabolism in thalassemia and sickle cell diseaseRaffaella Mariani, Paola Trombini, Matteo Pozzi, et al.
World Journal of Gastroenterology|February 6, 2009
Hepcidin modulation in human diseases: from research to clinicAlberto Piperno, Raffaella Mariani, Paola Trombini, et al.
European Journal of Case Reports in Internal Medicine|May 6, 2022
Rhabdomyolysis after Intravenous Ferric Gluconate: A Case ReportMara Botti, Alberto Piperno, Annalia Cianflone, et al.
Mediterranean Journal of Hematology and Infectious Diseases|March 22, 2021
Mental Well-Being in Patients with Transfusion-Dependent Anemias and Hemochromatosis during the SARS-CoV-2 PandemicRachele Piperno, Gabriella Bertazioli, Giulia Ravasi, et al.
AJNR. American Journal of Neuroradiology|March 12, 2005
MR imaging of cerebral cortical involvement in aceruloplasminemiaMarina Grisoli, Alberto Piperno, Luisa Chiapparini, et al.
British Journal of Haematology|November 28, 2008
Reduced expression of hepcidin in patients with myelodysplastic syndrome and myelofibrosis: the causes might be more heterogeneous than in thalassaemiaRaffaella Mariani, Sara Pelucchi, Matteo Pozzi, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|May 4, 2020
Ferroportin disease: A novel SLC40A1 mutationGiulia Ravasi, Sara Pelucchi, Andrea Russo, et al.
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