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Items: 11


Bacterial killing is enhanced by exogenous administration of lysozyme in the lungs.

Epaud R, Delestrain C, Weaver TE, Akinbi HT.

Respir Med Res. 2019 Jul 20;76:22-27. doi: 10.1016/j.resmer.2019.07.005. [Epub ahead of print]


Pulmonary Fibrosis in Children.

Nathan N, Sileo C, Thouvenin G, Berdah L, Delestrain C, Manali E, Papiris S, Léger PL, Pointe HDL, l'Hermine AC, Clement A.

J Clin Med. 2019 Aug 26;8(9). pii: E1312. doi: 10.3390/jcm8091312. Review.


Health-related quality of life in infants and children with interstitial lung disease.

Lauby C, Boelle PY, Abou Taam R, Bessaci K, Brouard J, Dalphin ML, Delacourt C, Delestrain C, Deschildre A, Dubus JC, Fayon M, Giovannini-Chami L, Houdouin V, Houzel A, Marguet C, Pin I, Reix P, Renoux MC, Schweitzer C, Tatopoulos A, Thumerelle C, Troussier F, Wanin S, Weiss L, Clement A, Epaud R, Nathan N.

Pediatr Pulmonol. 2019 Jun;54(6):828-836. doi: 10.1002/ppul.24308. Epub 2019 Mar 13.


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.

Respir Med. 2017 Aug;129:16-23. doi: 10.1016/j.rmed.2017.05.014. Epub 2017 May 26.


Deciphering the mechanism of Q145H SFTPC mutation unmasks a splicing defect and explains the severity of the phenotype.

Delestrain C, Simon S, Aissat A, Medina R, Decrouy X, Nattes E, Tarze A, Costes B, Fanen P, Epaud R.

Eur J Hum Genet. 2017 Jun;25(6):779-782. doi: 10.1038/ejhg.2017.36. Epub 2017 Mar 15.


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.

Pediatrics. 2017 Mar;139(3). pii: e20162988. doi: 10.1542/peds.2016-2988. Epub 2017 Feb 15.


Non-invasive CT screening for pulmonary arteriovenous malformations in children with confirmed hereditary hemorrhagic telangiectasia: Results from two pediatric centers.

Soysal N, Eyries M, Verlhac S, Escabasse V, Remus N, Tamalet A, Rioux JY, Franchi-Abella S, Vasile M, Robert S, Delestrain C, Hau I, Ducou-Le Pointe H, Soubrier F, Carette MF, Epaud R.

Pediatr Pulmonol. 2017 May;52(5):642-649. doi: 10.1002/ppul.23649. Epub 2017 Feb 6.


Cladribine improves lung cysts and pulmonary function in a child with histiocytosis.

Epaud R, Ducou Le Pointe H, Fasola S, Ploussard S, Delestrain C, Sileo C, Donadieu J.

Eur Respir J. 2015 Mar;45(3):831-3. doi: 10.1183/09031936.00146114. Epub 2014 Nov 13. No abstract available. Erratum in: Eur Respir J. 2016 Feb;47(2):692.


Combined pulmonary fibrosis and emphysema syndrome associated with ABCA3 mutations.

Epaud R, Delestrain C, Louha M, Simon S, Fanen P, Tazi A.

Eur Respir J. 2014 Feb;43(2):638-41. doi: 10.1183/09031936.00145213. Epub 2013 Oct 17. No abstract available.


[Lung diseases in children associated with inherited disorders of surfactant metabolism].

Delestrain C, Flamein F, Jonard L, Couderc R, Guillot L, Fanen P, Epaud R.

Rev Pneumol Clin. 2013 Aug;69(4):183-9. doi: 10.1016/j.pneumo.2013.05.002. Epub 2013 Jul 12. Review. French.


[Genetic disorders of surfactant].

Epaud R, Jonard L, Ducou-le-Pointe H, Delestrain C, Fanen P, Guillot L, Flamein F.

Arch Pediatr. 2012 Feb;19(2):212-9. doi: 10.1016/j.arcped.2011.12.004. Epub 2012 Jan 9. Review. French.


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