| Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis … A Goodeve, J Eikenboom, G Castaman, F Rodeghiero, AB Federici, ... Blood 109 (1), 112-121, 2007 | 470 | 2007 |
| Role of von Willebrand factor in the haemostasis F Peyvandi, I Garagiola, L Baronciani Blood Transfusion 9 (Suppl 2), s3, 2011 | 316 | 2011 |
| Clinical and molecular predictors of thrombocytopenia and risk of bleeding in patients with von Willebrand disease type 2B: a cohort study of 67 patients AB Federici, PM Mannucci, G Castaman, L Baronciani, P Bucciarelli, ... Blood, The Journal of the American Society of Hematology 113 (3), 526-534, 2009 | 312 | 2009 |
| The ADAMTS13‐von Willebrand factor axis in COVID‐19 patients I Mancini, L Baronciani, A Artoni, P Colpani, M Biganzoli, G Cozzi, ... Journal of Thrombosis and Haemostasis 19 (2), 513-521, 2021 | 226 | 2021 |
| Molecular defects in type 3 von Willebrand disease: updated results from 40 multiethnic patients L Baronciani, G Cozzi, MT Canciani, F Peyvandi, A Srivastava, ... Blood Cells, Molecules, and Diseases 30 (3), 264-270, 2003 | 150 | 2003 |
| Rapid purification of glucose-6-phosphate dehydrogenase from mammal's erythrocytes P Ninfali, I Orsenigo, L Baronciani, S Rapa Preparative biochemistry 20 (3-4), 297-309, 1990 | 101 | 1990 |
| Molecular Characterization of PK-LR Gene in Pyruvate Kinase–Deficient Italian Patients A Zanella, P Bianchi, L Baronciani, M Zappa, E Bredi, C Vercellati, ... Blood, The Journal of the American Society of Hematology 89 (10), 3847-3852, 1997 | 95 | 1997 |
| Molecular characterization of a multiethnic group of 21 patients with type 3 von Willebrand disease L Baronciani, G Cozzi, MT Canciani, F Peyvandi, A Srivastava, ... Thrombosis and haemostasis 84 (10), 536-540, 2000 | 92 | 2000 |
| Analysis of pyruvate kinase-deficiency mutations that produce nonspherocytic hemolytic anemia. L Baronciani, E Beutler Proceedings of the National Academy of Sciences 90 (9), 4324-4327, 1993 | 92 | 1993 |
| Abnormal VWF modifies megakaryocytopoiesis: studies of platelets and megakaryocyte cultures from patients with von Willebrand disease type 2B P Nurden, G Gobbi, A Nurden, J Enouf, I Youlyouz-Marfak, C Carubbi, ... Blood, The Journal of the American Society of Hematology 115 (13), 2649-2656, 2010 | 90 | 2010 |
| Molecular study of pyruvate kinase deficient patients with hereditary nonspherocytic hemolytic anemia. L Baronciani, E Beutler The Journal of clinical investigation 95 (4), 1702-1709, 1995 | 86 | 1995 |
| An association of candidate gene haplotypes and bleeding severity in von Willebrand disease (VWD) type 1 pedigrees TJ Kunicki, AB Federici, DR Salomon, JA Koziol, SR Head, TS Mondala, ... Blood 104 (8), 2359-2367, 2004 | 78 | 2004 |
| New glucose-6-phosphate dehydrogenase mutations from various ethnic groups E Beutler, B Westwood, JT Prchal, G Vaca, CS Bartsocas, L Baronciani | 78 | 1992 |
| Management of inherited von Willebrand disease in Italy: results from the retrospective study on 1234 patients AB Federici, P Bucciarelli, G Castaman, L Baronciani, MT Canciani, ... Seminars in thrombosis and hemostasis 37 (05), 511-521, 2011 | 67 | 2011 |
| A two‐centre comparative evaluation of new automated assays for von Willebrand factor ristocetin cofactor activity and antigen F Stufano, AS Lawrie, S La Marca, C Berbenni, L Baronciani, F Peyvandi Haemophilia 20 (1), 147-153, 2014 | 50 | 2014 |
| Molecular diagnosis of von Willebrand disease L Baronciani, A Goodeve, F Peyvandi Haemophilia 23 (2), 188-197, 2017 | 45 | 2017 |
| How we make an accurate diagnosis of von Willebrand disease L Baronciani, F Peyvandi Thrombosis Research 196, 579-589, 2020 | 40 | 2020 |
| Study of the molecular defects in glucose phosphate isomerase-deficient patients affected by chronic hemolytic anemia L Baronciani, A Zanella, P Bianchi, M Zappa, F Alfinito, N Tannoia, ... Blood 88 (6), 2306-2310, 1996 | 39 | 1996 |
| Study of the molecular defects in glucose phosphate isomerase (GPI) deficient patients affected by chronic hemolytic anemia. L Baronciani, A Zanella, P Bianchi, F Alfinito, A Iolascon, N Tannoia, ... Blood 86 (10), 523-523, 1995 | 39 | 1995 |
| Expression studies on a novel type 2B variant of the von Willebrand factor gene (R1308L) characterized by defective collagen binding L Baronciani, AB Federici, M Beretta, G Cozzi, MT Canciani, PM Mannucci Journal of Thrombosis and Haemostasis 3 (12), 2689-2694, 2005 | 38 | 2005 |
