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Biochemical Society Transactions|October 31, 2015
ABCA3, a key player in neonatal respiratory transition and genetic disorders of the surfactant systemDonatella Peca, Renato Cutrera, Andrea Masotti, et al.
Italian Journal of Pediatrics|March 2, 2016
Surfactant Protein C-associated interstitial lung disease; three different phenotypes of the same SFTPC mutationTeresa Salerno, Donatella Peca, Laura Menchini, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|October 29, 2015
New ATP-binding cassette A3 mutation causing surfactant metabolism dysfunction pulmonary type 3Fiammetta Piersigilli, Donatella Peca, Francesca Campi, et al.
Ultrastructural Pathology|September 20, 2013
Ultrastructural characterization of genetic diffuse lung diseases in infants and children: a cohort study and reviewArianna Citti, Donatella Peca, Stefania Petrini, et al.
Pediatric Pulmonology|September 3, 2013
Respiratory insufficiency in a newborn with congenital hypothyroidism due to a new mutation of TTF-1/NKX2.1 geneTeresa Salerno, Donatella Peca, Laura Menchini, et al.
Respiratory Research|August 27, 2011
Altered surfactant homeostasis and recurrent respiratory failure secondary to TTF-1 nuclear targeting defectDonatella Peca, Stefania Petrini, Chryssoula Tzialla, et al.
The European Respiratory Journal|June 16, 2012
Impaired surfactant protein B synthesis in infants with congenital diaphragmatic herniaPaola E Cogo, Manuela Simonato, Olivier Danhaive, et al.
European Journal of Human Genetics : EJHG|March 19, 2015
Clinical and ultrastructural spectrum of diffuse lung disease associated with surfactant protein C mutationsDonatella Peca, Renata Boldrini, Jan Johannson, et al.
The European Respiratory Journal|June 2, 2019
Phenotype characterisation of TBX4 mutation and deletion carriers with neonatal and paediatric pulmonary hypertensionCsaba Galambos, Mary P Mullen, Joseph T Shieh, et al.
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