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olivier danhaive
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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
2092017
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
1772020
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
1182020
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
1022008
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
962016
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
962011
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
802007
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
542019
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
512005
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
502006
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
482020
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
442020
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
432015
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
362020
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
312015
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
312015
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
302016
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
272013
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
252014
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
242013
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