| Autologous bone marrow-derived mesenchymal stromal cells in the treatment of fistulising Crohn's disease R Ciccocioppo, ME Bernardo, A Sgarella, R Maccario, MA Avanzini, ... Gut 60 (6), 788-798, 2011 | 663 | 2011 |
| New 40Ar/39Ar, stratigraphic and palaeoclimatic data on the Isernia la Pineta Lower Palaeolithic site, Molise, Italy M Coltorti, G Feraud, A Marzoli, C Peretto, T Ton-That, P Voinchet, ... Quaternary International 131 (1), 11-22, 2005 | 205 | 2005 |
| The same molecular mechanism at the maternal meiosis I produces mono-and dicentric 8p duplications. G Floridia, M Piantanida, A Minelli, C Dellavecchia, C Bonaglia, E Rossi, ... American journal of human genetics 58 (4), 785, 1996 | 131 | 1996 |
| Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15–20% of cases E Maserati, F Aprili, F Vinante, F Locatelli, G Amendola, A Zatterale, ... Genes, Chromosomes and Cancer 33 (1), 93-97, 2002 | 110 | 2002 |
| Hereditary haemorrhagic telangiectasia with extensive liver involvement is not caused by either HHT1 or HHT2. M Piantanida, E Buscarini, C Dellavecchia, A Minelli, A Rossi, L Buscarini, ... Journal of medical genetics 33 (6), 441-443, 1996 | 108 | 1996 |
| Constitutional trisomy 8 as first mutation in multistep carcinogenesis: clinical, cytogenetic, and molecular data on three cases L Seghezzi, E Maserati, A Minelli, C Dellavecchia, P Addis, F Locatelli, ... Genes, Chromosomes and Cancer 17 (2), 94-101, 1996 | 73 | 1996 |
| The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman‐Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome … E Maserati, B Pressato, R Valli, A Minelli, L Sainati, F Patitucci, C Marletta, ... British journal of haematology 145 (2), 190-197, 2009 | 67 | 2009 |
| The isochromosome i (7)(q10) carrying c. 258+ 2t> c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndrome A Minelli, E Maserati, E Nicolis, M Zecca, L Sainati, D Longoni, F Lo Curto, ... Leukemia 23 (4), 708-711, 2009 | 66 | 2009 |
| Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies E Maserati, A Minelli, B Pressato, R Valli, B Crescenzi, M Stefanelli, ... Genes, chromosomes and cancer 45 (4), 375-382, 2006 | 61 | 2006 |
| Ubiquitin/proteasome-rich particulate cytoplasmic structures (PaCSs) in the platelets and megakaryocytes of ANKRD26-related thrombocytopenia V Necchi, A Balduini, P Noris, S Barozzi, P Sommi, C Di Buduo, ... Thrombosis and haemostasis 109 (02), 263-271, 2013 | 60 | 2013 |
| Inv dup (8)(p21. 1→ 22.1): further case report and a new hypothesis on the origin of the chromosome abnormality M Gorinati, D Caufin, A Minelli, L Memo, G Gaspardo, A Dodero Clinical genetics 39 (1), 55-59, 1991 | 51 | 1991 |
| Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies A Minelli, E Maserati, G Rossi, ME Bernardo, P De Stefano, MP Cecchini, ... Genes, Chromosomes and Cancer 40 (3), 165-171, 2004 | 48 | 2004 |
| Familial partial monosomy 7 and myelodysplasia: different parental origin of the monosomy 7 suggests action of a mutator gene A Minelli, E Maserati, G Giudici, S Tosi, C Olivieri, L Bonvini, P De Filippi, ... Cancer genetics and cytogenetics 124 (2), 147-151, 2001 | 48 | 2001 |
| Incidence of Shwachman-Diamond syndrome A Minelli, C Danesino, E Nicolis, Z Cannioto, D Longoni, S Perobelli, ... Pediatric blood & cancer 59, 1334-1335, 2012 | 45 | 2012 |
| New ESR/U-series data for the early Middle Pleistocene site of Isernia la Pineta, Italy Q Shao, JJ Bahain, C Falgueres, C Peretto, M Arzarello, A Minelli, ... Radiation measurements 46 (9), 847-852, 2011 | 45 | 2011 |
| Isochromosome (7)(q10) in Shwachman syndrome without MDS/AML and role of chromosome 7 anomalies in myeloproliferative disorders E Maserati, A Minelli, C Olivieri, L Bonvini, A Marchi, M Bozzola, ... Cancer genetics and cytogenetics 121 (2), 167-171, 2000 | 41 | 2000 |
| D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p) A Minelli, G Floridia, E Rossi, M Clementi, R Tenconi, L Camurri, ... Human genetics 92, 391-396, 1993 | 38 | 1993 |
| A homozygous missense arginine to histidine substitution at position 482 of the β-galactosidase in an Italian infantile GM1-gangliosidosis patient G Mosna, S Fattore, G Tubiello, S Brocca, M Trubia, E Gianazza, R Gatti, ... Human genetics 90, 247-250, 1992 | 29 | 1992 |
| Shwachman‐Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability R Valli, A Minelli, M Galbiati, G D'Amico, A Frattini, G Montalbano, ... British journal of haematology 184 (6), 974-981, 2019 | 26 | 2019 |
| Shwachman-Diamond syndrome and type 1 diabetes mellitus: more than a chance association? S Gana, L Sainati, MR Frau, C Monciotti, F Poli, Z Cannioto, M Comelli, ... Experimental and clinical endocrinology & diabetes, 610-612, 2011 | 26 | 2011 |
