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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 |
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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 | 339 | 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 |
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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 |
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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 |
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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 | 178 | 2010 |
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