| COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement F Diomedi-Camassei, S Di Giandomenico, FM Santorelli, G Caridi, ... Journal of the American Society of Nephrology 18 (10), 2773-2780, 2007 | 379 | 2007 |
| Infant high-grade gliomas comprise multiple subgroups characterized by novel targetable gene fusions and favorable outcomes M Clarke, A Mackay, B Ismer, JC Pickles, RG Tatevossian, S Newman, ... Cancer discovery 10 (7), 942-963, 2020 | 244 | 2020 |
| Semaphorin 3B–associated membranous nephropathy is a distinct type of disease predominantly present in pediatric patients S Sethi, H Debiec, B Madden, M Vivarelli, MC Charlesworth, A Ravindran, ... Kidney international 98 (5), 1253-1264, 2020 | 205 | 2020 |
| Long term follow up of children with myocarditis treated by immunosuppression and of children with dilated cardiomyopathy MG Gagliardi, M Bevilacqua, C Bassano, B Leonardi, R Boldrini, ... Heart 90 (10), 1167-1171, 2004 | 102 | 2004 |
| Impaired mitophagy links mitochondrial disease to epithelial stress in methylmalonyl-CoA mutase deficiency A Luciani, A Schumann, M Berquez, Z Chen, D Nieri, M Failli, H Debaix, ... Nature communications 11 (1), 970, 2020 | 99 | 2020 |
| SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder V Del Dotto, F Ullah, I Di Meo, P Magini, M Gusic, A Maresca, L Caporali, ... The Journal of clinical investigation 130 (1), 108-125, 2020 | 91 | 2020 |
| Malignant pancreatic endocrine tumor in a child with tuberous sclerosis P Francalanci, F Diomedi-Camassei, C Purificato, FM Santorelli, ... The American journal of surgical pathology 27 (10), 1386-1389, 2003 | 91 | 2003 |
| FGFR1: TACC1 fusion is a frequent event in molecularly defined extraventricular neurocytoma P Sievers, D Stichel, D Schrimpf, F Sahm, C Koelsche, DE Reuss, ... Acta neuropathologica 136, 293-302, 2018 | 75 | 2018 |
| Role of immunohistochemistry in the identification of supratentorial C11ORF95-RELA fused ependymoma in routine neuropathology M Gessi, M Giagnacovo, P Modena, G Elefante, F Gianno, FR Buttarelli, ... The American journal of surgical pathology 43 (1), 56-63, 2019 | 68 | 2019 |
| Genetic homogeneity but IgG subclass–dependent clinical variability of alloimmune membranous nephropathy with anti-neutral endopeptidase antibodies M Vivarelli, F Emma, T Pellé, C Gerken, S Pedicelli, F Diomedi-Camassei, ... Kidney International 87 (3), 602-609, 2015 | 67 | 2015 |
| Clinical significance of CXC chemokine receptor-4 and c-Met in childhood rhabdomyosarcoma F Diomedi-Camassei, HP McDowell, MA De Ioris, S Uccini, P Altavista, ... Clinical Cancer Research 14 (13), 4119-4127, 2008 | 61 | 2008 |
| Expression of the lipogenic enzyme fatty acid synthase (FAS) in retinoblastoma and its correlation with tumor aggressiveness FD Camassei, R Cozza, A Acquaviva, A Jenkner, L Ravà, R Gareri, ... Investigative ophthalmology & visual science 44 (6), 2399-2403, 2003 | 58 | 2003 |
| Dual IGF1R/IR inhibitors in combination with GD2-CAR T-cells display a potent anti-tumor activity in diffuse midline glioma H3K27M-mutant E de Billy, M Pellegrino, D Orlando, G Pericoli, R Ferretti, P Businaro, ... Neuro-oncology 24 (7), 1150-1163, 2022 | 56 | 2022 |
| BRAF V600E Inhibitor (Vemurafenib) for BRAF V600E Mutated Low Grade Gliomas F Del Bufalo, G Ceglie, A Cacchione, I Alessi, GS Colafati, A Carai, ... Frontiers in oncology 8, 526, 2018 | 55 | 2018 |
| Solitary crystal-storing histiocytosis of the tongue in a patient with rheumatoid arthritis and polyclonal hypergammaglobulinemia C Bosman, FD Camassei, R Boldrini, FR Piro Archives of pathology & laboratory medicine 122 (10), 920, 1998 | 48 | 1998 |
| Collapsing glomerulopathy associated with inherited mitochondrial injury L Barisoni, F Diomedi-Camassei, FM Santorelli, G Caridi, DB Thomas, ... Kidney international 74 (2), 237-243, 2008 | 47 | 2008 |
| IDO1 involvement in mTOR pathway: a molecular mechanism of resistance to mTOR targeting in medulloblastoma V Folgiero, E Miele, A Carai, E Ferretti, V Alfano, A Po, V Bertaina, ... Oncotarget 7 (33), 52900, 2016 | 44 | 2016 |
| Eosinophilic esophagitis and Barrett’s esophagus: an occasional association or an overlap disease? Esophageal ‘double trouble’in two children P Francalanci, P De Angelis, F Minnei, F Diomedi Camassei, F Torroni, ... Digestion 77 (1), 16-19, 2008 | 42 | 2008 |
| Infant high grade gliomas comprise multiple subgroups characterized by novel targetable gene fusions and favorable outcomes. Cancer Discov; 2020 M Clarke, A Mackay, B Ismer, JC Pickles, RG Tatevossian, S Newman, ... CD-19-1030.[Europe PMC free article][Abstract][CrossRef][Academic Search] 10 …, 2020 | 40 | 2020 |
| Identification and subcellular localization of a new cystinosin isoform A Taranta, S Petrini, A Palma, L Mannucci, MJ Wilmer, V De Luca, ... American Journal of Physiology-Renal Physiology 294 (5), F1101-F1108, 2008 | 40 | 2008 |
