| Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus BH Anderson, PR Kasher, J Mayer, M Szynkiewicz, EM Jenkinson, ... Nature genetics 44 (3), 338-342, 2012 | 284 | 2012 |
| Effect of multisensory stimulation on analgesia in term neonates: a randomized controlled trial CV Bellieni, F Bagnoli, S Perrone, A Nenci, DM Cordelli, M Fusi, ... Pediatric research 51 (4), 460-463, 2002 | 256 | 2002 |
| Analgesic effect of watching TV during venipuncture CV Bellieni, DM Cordelli, M Raffaelli, B Ricci, G Morgese, G Buonocore Archives of disease in childhood 91 (12), 1015-1017, 2006 | 207 | 2006 |
| Sensorial Saturation: An Effective Analgesic Tool for Heel-Prick in Preterm Infants: A Prospective Randomized Trial1 CV Bellieni, G Buonocore, A Nenci, N Franci, DM Cordelli, F Bagnoli Neonatology 80 (1), 15-18, 2001 | 165 | 2001 |
| Sensorial saturation for neonatal analgesia CV Bellieni, DM Cordelli, S Marchi, S Ceccarelli, S Perrone, M Maffei, ... The Clinical journal of pain 23 (3), 219-221, 2007 | 125 | 2007 |
| Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts EM Jenkinson, MP Rodero, PR Kasher, C Uggenti, A Oojageer, ... Nature genetics 48 (10), 1185-1192, 2016 | 122 | 2016 |
| Efficacy and safety of levetiracetam: an add-on trial in children with refractory epilepsy S Grosso, E Franzoni, G Coppola, P Iannetti, A Verrotti, DM Cordelli, ... Seizure 14 (4), 248-253, 2005 | 110 | 2005 |
| Cry features reflect pain intensity in term newborns: an alarm threshold CV Bellieni, R Sisto, DM Cordelli, G Buonocore Pediatric research 55 (1), 142-146, 2004 | 107 | 2004 |
| Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patients R Carrozzo, D Verrigni, M Rasmussen, R De Coo, H Amartino, M Bianchi, ... Journal of inherited metabolic disease 39, 243-252, 2016 | 92 | 2016 |
| Efficacy and safety of levetiracetam in infants and young children with refractory epilepsy S Grosso, DM Cordelli, E Franzoni, G Coppola, G Capovilla, N Zamponi, ... Seizure 16 (4), 345-350, 2007 | 90 | 2007 |
| Phenotype and genotype of 87 patients with Mowat–Wilson syndrome and recommendations for care I Ivanovski, O Djuric, SG Caraffi, D Santodirocco, M Pollazzon, S Rosato, ... Genetics in Medicine 20 (9), 965-975, 2018 | 81 | 2018 |
| Symmetric polymicrogyria and pachygyria associated with TUBB2B gene mutations R Guerrini, D Mei, DM Cordelli, D Pucatti, E Franzoni, E Parrini European journal of human genetics 20 (9), 995-998, 2012 | 76 | 2012 |
| PRES in children undergoing hematopoietic stem cell or solid organ transplantation R Masetti, DM Cordelli, D Zama, F Vendemini, C Biagi, E Franzoni, ... Pediatrics 135 (5), 890-901, 2015 | 68 | 2015 |
| Inter-observer reliability of two pain scales for newborns CV Bellieni, DM Cordelli, C Caliani, C Palazzi, N Franci, S Perrone, ... Early human development 83 (8), 549-552, 2007 | 61 | 2007 |
| Hot water epilepsy and focal malformation of the parietal cortex development S Grosso, MA Farnetani, S Francione, P Galluzzi, G Vatti, DM Cordelli, ... Brain and Development 26 (7), 490-493, 2004 | 60 | 2004 |
| Neuroimaging findings in Mowat–Wilson syndrome: a study of 54 patients L Garavelli, I Ivanovski, SG Caraffi, D Santodirocco, M Pollazzon, ... Genetics in Medicine 19 (6), 691-700, 2017 | 59 | 2017 |
| Status epilepticus as a main manifestation of posterior reversible encephalopathy syndrome after pediatric hematopoietic stem cell transplantation DM Cordelli, R Masetti, B Bernardi, G Barcia, V Gentile, C Biagi, A Prete, ... Pediatric Blood & Cancer 58 (5), 785-790, 2012 | 57 | 2012 |
| Sleep disorders reveal distress among children and adolescents during the Covid-19 first wave: results of a large web-based Italian survey A Dondi, A Fetta, J Lenzi, F Morigi, E Candela, A Rocca, DM Cordelli, ... Italian journal of pediatrics 47 (1), 130, 2021 | 56 | 2021 |
| Development and validation of the ABC pain scale for healthy full‐term babies CV Bellieni, F Bagnoli, R Sisto, L Neri, D Cordelli, G Buonocore Acta Paediatrica 94 (10), 1432-1436, 2005 | 56 | 2005 |
| Epilepsy in Mowat–Wilson syndrome: Delineation of the electroclinical phenotype DM Cordelli, L Garavelli, S Savasta, A Guerra, A Pellicciari, L Giordano, ... American Journal of Medical Genetics Part A 161 (2), 273-284, 2013 | 53 | 2013 |
