| The Montreux definition of neonatal ARDS: biological and clinical background behind the description of a new entity D De Luca, AH Van Kaam, DG Tingay, SE Courtney, O Danhaive, ... The Lancet Respiratory Medicine 5 (8), 657-666, 2017 | 209 | 2017 |
| Novel Coronavirus disease (COVID-19) in newborns and infants: what we know so far DU De Rose, F Piersigilli, MP Ronchetti, A Santisi, I Bersani, A Dotta, ... Italian journal of pediatrics 46 (1), 1-8, 2020 | 177 | 2020 |
| COVID-19 in a 26-week preterm neonate F Piersigilli, K Carkeek, C Hocq, B Van Grambezen, C Hubinont, ... The Lancet Child & Adolescent Health 4 (6), 476-478, 2020 | 118 | 2020 |
| Spectrum of MMACHC mutations in Italian and Portuguese patients with combined methylmalonic aciduria and homocystinuria, cblC type C Nogueira, C Aiello, R Cerone, E Martins, U Caruso, I Moroni, C Rizzo, ... Molecular genetics and metabolism 93 (4), 475-480, 2008 | 102 | 2008 |
| Rapid and safe response to low‐dose carbamazepine in neonatal epilepsy TT Sands, M Balestri, G Bellini, SB Mulkey, O Danhaive, EH Bakken, ... Epilepsia 57 (12), 2019-2030, 2016 | 96 | 2016 |
| Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia MJ Wat, D Veenma, J Hogue, AM Holder, Z Yu, JJ Wat, N Hanchard, ... Journal of medical genetics 48 (5), 299-307, 2011 | 96 | 2011 |
| Unexplained neonatal respiratory distress due to congenital surfactant deficiency M Somaschini, LM Nogee, I Sassi, O Danhaive, S Presi, R Boldrini, ... The Journal of pediatrics 150 (6), 649-653. e1, 2007 | 80 | 2007 |
| Phenotype characterisation of TBX4 mutation and deletion carriers with neonatal and paediatric pulmonary hypertension C Galambos, MP Mullen, JT Shieh, N Schwerk, MJ Kielt, N Ullmann, ... European Respiratory Journal 54 (2), 2019 | 54 | 2019 |
| Pulmonary hypertension and right ventricular dysfunction in growth-restricted, extremely low birth weight neonates O Danhaive, R Margossian, T Geva, S Kourembanas Journal of Perinatology 25 (7), 495-499, 2005 | 51 | 2005 |
| Birth weight and McGoon Index predict mortality in newborn infants with congenital diaphragmatic hernia G Casaccia, F Crescenzi, A Dotta, I Capolupo, A Braguglia, O Danhaive, ... Journal of pediatric surgery 41 (1), 25-28, 2006 | 50 | 2006 |
| Surfactant replacement therapy: from biological basis to current clinical practice R Hentschel, K Bohlin, A van Kaam, H Fuchs, O Danhaive Pediatric research 88 (2), 176-183, 2020 | 48 | 2020 |
| Study Group of Neonatal Infectious Diseases of The Italian Society of Neonatology (SIN). Novel Coronavirus disease (COVID-19) in newborns and infants: what we know so far DU De Rose, F Piersigilli, MP Ronchetti, A Santisi, I Bersani, A Dotta, ... Ital J Pediatr 46 (1), 56, 2020 | 44 | 2020 |
| Dysregulation of locus coeruleus development in congenital central hypoventilation syndrome H Nobuta, MR Cilio, O Danhaive, HH Tsai, S Tupal, SM Chang, A Murnen, ... Acta neuropathologica 130, 171-183, 2015 | 43 | 2015 |
| Nutrients and microbiota in lung diseases of prematurity: the placenta-gut-lung triangle F Piersigilli, B Van Grambezen, C Hocq, O Danhaive Nutrients 12 (2), 469, 2020 | 36 | 2020 |
| ABCA3, a key player in neonatal respiratory transition and genetic disorders of the surfactant system D Peca, R Cutrera, A Masotti, R Boldrini, O Danhaive Biochemical Society Transactions 43 (5), 913-919, 2015 | 31 | 2015 |
| Clinical and ultrastructural spectrum of diffuse lung disease associated with surfactant protein C mutations D Peca, R Boldrini, J Johannson, JT Shieh, A Citti, S Petrini, T Salerno, ... European Journal of Human Genetics 23 (8), 1033-1041, 2015 | 31 | 2015 |
| Surfactant Protein C-associated interstitial lung disease; three different phenotypes of the same SFTPC mutation T Salerno, D Peca, L Menchini, A Schiavino, R Boldrini, F Esposito, ... Italian journal of pediatrics 42, 1-4, 2016 | 30 | 2016 |
| Ultrastructural characterization of genetic diffuse lung diseases in infants and children: a cohort study and review A Citti, D Peca, S Petrini, R Cutrera, P Biban, C Haass, R Boldrini, ... Ultrastructural pathology 37 (5), 356-365, 2013 | 27 | 2013 |
| Respiratory insufficiency in a newborn with congenital hypothyroidism due to a new mutation of TTF‐1/NKX2. 1 gene T Salerno, D Peca, L Menchini, A Schiavino, F Petreschi, F Occasi, ... Pediatric pulmonology 49 (3), E42-E44, 2014 | 25 | 2014 |
| Impaired surfactant protein B synthesis in infants with congenital diaphragmatic hernia PE Cogo, M Simonato, O Danhaive, G Verlato, G Cobellis, F Savignoni, ... European Respiratory Journal 41 (3), 677-682, 2013 | 24 | 2013 |
paola carreraGroup Leader, Ospedale San Raffaele, MilanoVerified email at hsr.it
