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British Journal of Haematology|June 15, 2007
Modern treatment of thalassaemia intermediaCaterina Borgna-PignattiHematology/Oncology Clinics of North America|July 28, 2014
Transfusional iron overload and iron chelation therapy in thalassemia major and sickle cell diseaseMaria Marsella, Caterina Borgna-PignattiClinical Therapeutics|November 1, 2015
Iron Chelation in Thalassemia MajorCaterina Borgna-Pignatti, Maria MarsellaExpert Review of Hematology|October 6, 2016
Pica as a manifestation of iron deficiencyCaterina Borgna-Pignatti, Sara ZanellaExpert Review of Hematology|June 15, 2011
Complications of thalassemia major and their treatmentCaterina Borgna-Pignatti, Maria Rita GamberiniExpert Review of Hematology|December 22, 2016
Can the surgical tourniquet be used in patients with sickle cell disease or trait? A review of the literatureMarco Pignatti, Sara Zanella, Caterina Borgna-PignattiStroke Research and Treatment|July 22, 2011
Ischemic stroke in infants and children: practical management in emergencySara Ciccone, Michela Cappella, Caterina Borgna-PignattiThe Journal of Pediatrics|July 22, 2009
Thiamine-responsive megaloblastic anemia syndrome: long term follow-upCaterina Borgna-Pignatti, Milena Azzalli, Stefania PedrettiAnnals of the New York Academy of Sciences|August 18, 2010
The natural history of thalassemia intermediaCaterina Borgna-Pignatti, Maria Marsella, Nicolò ZanforlinAnnals of the New York Academy of Sciences|August 18, 2010
Better survival and less cardiac morbidity in female patients with thalassemia major: a review of the literatureMaria Marsella, Alessia Pepe, Caterina Borgna-PignattiPageof 5