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Page 1
Characteristics of endobronchial primitive tumors in children.
Eyssartier E, Ang P, Bonnemaison E, Gibertini I, Diot P, Carpentier E, Chantepie A, Leclair MD, Brouard J, Boutard P, Deneuville E, Marie-Cardine A, Lardy H. Eyssartier E, et al. Among authors: gibertini i. Pediatr Pulmonol. 2014 Jun;49(6):E121-5. doi: 10.1002/ppul.22987. Epub 2014 Feb 16. Pediatr Pulmonol. 2014. PMID: 24532419
Predicting the risk of respiratory distress in newborns with congenital pulmonary malformations.
Delacourt C, Bertille N, Salomon LJ, Rahshenas M, Benachi A, Bonnard A, Choupeaux L, Fouquet V, Goua V, Hameury F, Hervieux E, Jouannic JM, Khen-Dunlop N, Le Bouar G, Massardier J, Roditis L, Rosenblatt J, Sartor A, Thong-Vanh C, Lelong N, Khoshnood B; , for the MALFPULM study group; members of the MALFPULM study group:. Delacourt C, et al. Eur Respir J. 2022 Feb 3;59(2):2100949. doi: 10.1183/13993003.00949-2021. Print 2022 Feb. Eur Respir J. 2022. PMID: 34266941 Free article.
A national internet-linked based database for pediatric interstitial lung diseases: the French network.
Nathan N, Taam RA, Epaud R, Delacourt C, Deschildre A, Reix P, Chiron R, de Pontbriand U, Brouard J, Fayon M, Dubus JC, Giovannini-Chami L, Bremont F, Bessaci K, Schweitzer C, Dalphin ML, Marguet C, Houdouin V, Troussier F, Sardet A, Hullo E, Gibertini I, Mahloul M, Michon D, Priouzeau A, Galeron L, Vibert JF, Thouvenin G, Corvol H, Deblic J, Clement A; French RespiRare® Group. Nathan N, et al. Among authors: gibertini i. Orphanet J Rare Dis. 2012 Jun 15;7:40. doi: 10.1186/1750-1172-7-40. Orphanet J Rare Dis. 2012. PMID: 22704798 Free PMC article.
Respiratory Morbidity in Infants Born With a Congenital Lung Malformation.
Delestrain C, Khen-Dunlop N, Hadchouel A, Cros P, Ducoin H, Fayon M, Gibertini I, Labbé A, Labouret G, Lebras MN, Lezmi G, Madhi F, Thouvenin G, Thumerelle C, Delacourt C. Delestrain C, et al. Among authors: gibertini i. Pediatrics. 2017 Mar;139(3):e20162988. doi: 10.1542/peds.2016-2988. Epub 2017 Feb 15. Pediatrics. 2017. PMID: 28202768
Heterogeneity of lung disease associated with NK2 homeobox 1 mutations.
Nattes E, Lejeune S, Carsin A, Borie R, Gibertini I, Balinotti J, Nathan N, Marchand-Adam S, Thumerelle C, Fauroux B, Bosdure E, Houdouin V, Delestrain C, Louha M, Couderc R, De Becdelievre A, Fanen P, Funalot B, Crestani B, Deschildre A, Dubus JC, Epaud R. Nattes E, et al. Among authors: gibertini i. Respir Med. 2017 Aug;129:16-23. doi: 10.1016/j.rmed.2017.05.014. Epub 2017 May 26. Respir Med. 2017. PMID: 28732825 Free article. Clinical Trial.
Pulmonary hemosiderosis in children with Down syndrome: a national experience.
Alimi A, Taytard J, Abou Taam R, Houdouin V, Forgeron A, Lubrano Lavadera M, Cros P, Gibertini I, Derelle J, Deschildre A, Thumerelle C, Epaud R, Reix P, Fayon M, Roullaud S, Troussier F, Renoux MC, de Blic J, Leyronnas S, Thouvenin G, Perisson C, Ravel A, Clement A, Corvol H, Nathan N; French RespiRare® group. Alimi A, et al. Among authors: gibertini i. Orphanet J Rare Dis. 2018 Apr 20;13(1):60. doi: 10.1186/s13023-018-0806-6. Orphanet J Rare Dis. 2018. PMID: 29678139 Free PMC article.
Deciphering an isolated lung phenotype of NKX2-1 frameshift pathogenic variant.
Delestrain C, Aissat A, Nattes E, Gibertini I, Lacroze V, Simon S, Decrouy X, de Becdelièvre A, Fanen P, Epaud R. Delestrain C, et al. Among authors: gibertini i. Front Pediatr. 2023 Jan 17;10:978598. doi: 10.3389/fped.2022.978598. eCollection 2022. Front Pediatr. 2023. PMID: 36733766 Free PMC article.
Cancer-associated Mutations in Congenital Pulmonary Malformations: A Prospective Cohort.
Garinet S, Rahshenas M, Galmiche-Rolland L, Abbo O, Bonnard A, Hameury F, Khen-Dunlop N, Khoshnood B, Blons H, Delacourt C; MALFPULM study group. Garinet S, et al. Am J Respir Crit Care Med. 2023 Mar 1;207(5):615-619. doi: 10.1164/rccm.202208-1573LE. Am J Respir Crit Care Med. 2023. PMID: 36288557 Free PMC article. No abstract available.