| Heparin-induced thrombocytopenia: towards consensus TE Warkentin, BH Chong, A Greinacher Thrombosis and haemostasis 59 (01), 1-7, 1998 | 755 | 1998 |
| MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single … M Seri, A Pecci, F Di Bari, R Cusano, M Savino, E Panza, A Nigro, P Noris, ... Medicine 82 (3), 203-215, 2003 | 402 | 2003 |
| Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium. M Seri, R Cusano, S Gangarossa, G Caridi, D Bordo, L Nigro, ... Nature genetics 26 (1), 103-105, 2000 | 398 | 2000 |
| Polypharmacy, length of hospital stay, and in-hospital mortality among elderly patients in internal medicine wards. The REPOSI study A Nobili, G Licata, F Salerno, L Pasina, M Tettamanti, C Franchi, ... European journal of clinical pharmacology 67, 507-519, 2011 | 388 | 2011 |
| Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemia L Noetzli, RW Lo, AB Lee-Sherick, M Callaghan, P Noris, A Savoia, ... Nature genetics 47 (5), 535-538, 2015 | 338 | 2015 |
| 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 |
| Inherited thrombocytopenias: from genes to therapy CL Balduini, A Iolascon, A Savoia haematologica 87 (8), 860-880, 2002 | 290 | 2002 |
| Age-and sex-related variations in platelet count in Italy: a proposal of reference ranges based on 40987 subjects' data G Biino, I Santimone, C Minelli, R Sorice, B Frongia, M Traglia, S Ulivi, ... PloS one 8 (1), e54289, 2013 | 264 | 2013 |
| Recent advances in the understanding and management of MYH9‐related inherited thrombocytopenias CL Balduini, A Pecci, A Savoia British journal of haematology 154 (2), 161-174, 2011 | 252 | 2011 |
| Protein Z-dependent regulation of coagulation GJ Broze Jr Thrombosis and haemostasis 86 (07), 08-13, 2001 | 238 | 2001 |
| Mutations in the 5′ UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2 T Pippucci, A Savoia, S Perrotta, N Pujol-Moix, P Noris, G Castegnaro, ... The American Journal of Human Genetics 88 (1), 115-120, 2011 | 237 | 2011 |
| New roles for mean platelet volume measurement in the clinical practice? P Noris, F Melazzini, CL Balduini Platelets 27 (7), 607-612, 2016 | 235 | 2016 |
| Clinical and genetic aspects of Bernard-Soulier syndrome: searching for genotype/phenotype correlations A Savoia, A Pastore, D De Rocco, E Civaschi, M Di Stazio, R Bottega, ... haematologica 96 (3), 417, 2011 | 235 | 2011 |
| Heparin-induced thrombocytopenia: a clinicopathologic syndrome TE Warkentin Thrombosis and haemostasis 82 (08), 439-447, 1999 | 227 | 1999 |
| Position of nonmuscle myosin heavy chain IIA (NMMHC‐IIA) mutations predicts the natural history of MYH9‐related disease A Pecci, E Panza, N Pujol‐Moix, C Klersy, F Di Bari, V Bozzi, P Gresele, ... Human mutation 29 (3), 409-417, 2008 | 219 | 2008 |
| MYH9‐Related Disease: A Novel Prognostic Model to Predict the Clinical Evolution of the Disease Based on Genotype–Phenotype Correlations A Pecci, C Klersy, P Gresele, KJD Lee, D De Rocco, V Bozzi, G Russo, ... Human Mutation 35 (2), 236-247, 2014 | 204 | 2014 |
| ANKRD26-related thrombocytopenia and myeloid malignancies P Noris, R Favier, MC Alessi, AE Geddis, S Kunishima, PG Heller, ... Blood, The Journal of the American Society of Hematology 122 (11), 1987-1989, 2013 | 201 | 2013 |
| Autosomal dominant macrothrombocytopenia in Italy is most frequently a type of heterozygous Bernard-Soulier syndrome A Savoia, CL Balduini, M Savino, P Noris, M Del Vecchio, S Perrotta, ... Blood, The Journal of the American Society of Hematology 97 (5), 1330-1335, 2001 | 200 | 2001 |
| High versus standard dose methylprednisolone in the acute phase of idiopathic thrombotic thrombocytopenic purpura: a randomized study CL Balduini, L Gugliotta, M Luppi, L Laurenti, C Klersy, C Pieresca, ... Annals of hematology 89, 591-596, 2010 | 176 | 2010 |
| Eltrombopag for the treatment of the inherited thrombocytopenia deriving from MYH9 mutations A Pecci, P Gresele, C Klersy, A Savoia, P Noris, T Fierro, V Bozzi, ... Blood, The Journal of the American Society of Hematology 116 (26), 5832-5837, 2010 | 175 | 2010 |
