| Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families P Noris, S Perrotta, M Seri, A Pecci, C Gnan, G Loffredo, N Pujol-Moix, ... Blood, The Journal of the American Society of Hematology 117 (24), 6673-6680, 2011 | 319 | 2011 |
| Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano … P Noris, S Perrotta, R Bottega, A Pecci, F Melazzini, E Civaschi, S Russo, ... haematologica 97 (1), 82, 2012 | 107 | 2012 |
| Endocrine function and bone disease during long‐term chelation therapy with deferasirox in patients with β‐thalassemia major M Casale, S Citarella, A Filosa, E De Michele, F Palmieri, A Ragozzino, ... American journal of hematology 89 (12), 1102-1106, 2014 | 96 | 2014 |
| Multiparametric cardiac magnetic resonance survey in children with thalassemia major: a multicenter study M Casale, A Meloni, A Filosa, L Cuccia, V Caruso, G Palazzi, ... Circulation: Cardiovascular Imaging 8 (8), e003230, 2015 | 80 | 2015 |
| Splenectomy for hereditary spherocytosis: complete, partial or not at all? M Casale, S Perrotta Expert review of hematology 4 (6), 627-635, 2011 | 52 | 2011 |
| Diagnosis and management of newly diagnosed childhood autoimmune haemolytic anaemia. Recommendations from the Red Cell Study Group of the Paediatric Haemato-Oncology Italian … S Ladogana, M Maruzzi, P Samperi, S Perrotta, GC Del Vecchio, ... Blood Transfusion 15 (3), 259, 2017 | 50 | 2017 |
| Congenital erythrocytosis associated with gain-of-function HIF2A gene mutations and erythropoietin levels in the normal range S Perrotta, DP Stiehl, F Punzo, S Scianguetta, A Borriello, D Bencivenga, ... haematologica 98 (10), 1624, 2013 | 41 | 2013 |
| Effect of splenectomy on iron balance in patients with β‐thalassemia major: a long‐term follow‐up M Casale, P Cinque, P Ricchi, S Costantini, A Spasiano, L Prossomariti, ... European Journal of Haematology 91 (1), 69-73, 2013 | 38 | 2013 |
| Hydroxyurea prescription, availability and use for children with sickle cell disease in Italy: Results of a National Multicenter survey R Colombatti, G Palazzi, N Masera, LD Notarangelo, E Bonetti, P Samperi, ... Pediatric blood & cancer 65 (2), e26774, 2018 | 35 | 2018 |
| Organizing national responses for rare blood disorders: the Italian experience with sickle cell disease in childhood R Colombatti, S Perrotta, P Samperi, M Casale, N Masera, G Palazzi, ... Orphanet Journal of Rare Diseases 8, 1-9, 2013 | 32 | 2013 |
| Long-term treatment with deferiprone enhances left ventricular ejection function when compared to deferoxamine in patients with thalassemia major A Filosa, A Vitrano, P Rigano, G Calvaruso, R Barone, M Capra, L Cuccia, ... Blood Cells, Molecules, and Diseases 51 (2), 85-88, 2013 | 28 | 2013 |
| Extramedullary haematopoiesis correlates with genotype and absence of cardiac iron overload in polytransfused adults with thalassaemia P Ricchi, M Ammirabile, A Spasiano, S Costantini, T Di Matola, A Pepe, ... Blood Transfusion 12 (Suppl 1), s124, 2014 | 25 | 2014 |
| Congenital Dyserythropoietic Anemia Type II: molecular analysis and expression of the SEC23B Gene F Punzo, AM Bertoli-Avella, S Scianguetta, F Della Ragione, M Casale, ... Orphanet Journal of Rare Diseases 6, 1-9, 2011 | 22 | 2011 |
| HNF-1β mutation affects PKD2 and SOCS3 expression causing renal cysts and diabetes in MODY5 kindred. S Mancusi, A La Manna, G Bellini, S Scianguetta, D Roberti, M Casale, ... Journal of nephrology 26 (1), 207-212, 2013 | 19 | 2013 |
| Hereditary hypochromic microcytic anemia associated with loss-of-function DMT1 gene mutations and absence of liver iron overload. M Casale, A Borriello, S Scianguetta, D Roberti, M Caiazza, ... American journal of hematology 93 (3), E58-E60, 2017 | 10 | 2017 |
| Nephrolithiasis in patients exposed to deferasirox and desferioxamine: probably an age-linked event with different effects on some renal parameters P Ricchi, M Ammirabile, S Costantini, A Spasiano, T Di Matola, P Cinque, ... Annals of hematology 93, 525-527, 2014 | 10 | 2014 |
| Subarachnoid haemorrhage and cerebral vasculopathy in a child with sickle cell anaemia B Inusa, M Casale, C Booth, S Lucas Case Reports 2014, bcr2014205464, 2014 | 7 | 2014 |
| Association between serum ferritin and liver iron concentration with cardiac iron in pediatric thalassemia major patients A Pepe, A Meloni, M Casale, MG Neri, PP Bitti, S Macchi, GR Giugno, ... Blood, The Journal of the American Society of Hematology 126 (23), 956-956, 2015 | 4 | 2015 |
| Linee-guida per la gestione della malattia drepanocitica in eta’pediatrica in Italia M Casale, ML Casciana, A Ciliberti Associazione Italiana Ematologia Oncologia Pediatrica, 2018 | 2 | 2018 |
| The Cardiomyopathy of Sickle Cell Disease O Niss, CT Quinn Sickle Cell Disease-Pain and Common Chronic Complications, 2016 | 2 | 2016 |
