I. Gibertini

Heterogeneity of lung disease associated with NK2 homeobox 1 mutations.

R. Epaud, R. Borie, E. Bosdure, 2017, Respiratory medicine.

Characteristics of endobronchial primitive tumors in children

P. Diot, M. Leclair, É. Carpentier, 2014, Pediatric pulmonology.

Pulmonary hemosiderosis in children with Down syndrome: a national experience

P. Reix, R. Epaud, A. Clément, 2018, Orphanet Journal of Rare Diseases.

Respiratory Morbidity in Infants Born With a Congenital Lung Malformation

C. Delacourt, A. Labbé, G. Thouvenin, 2017, Pediatrics.

A national internet-linked based database for pediatric interstitial lung diseases: the French network

C. Delacourt, J. Vibert, P. Reix, 2012, Orphanet Journal of Rare Diseases.

Deciphering an isolated lung phenotype of NKX2-1 frameshift pathogenic variant

S. Simon, R. Epaud, X. Decrouy, 2023, Frontiers in Pediatrics.