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First Genotype-Phenotype Study in TBX4 Syndrome: Gain-of-Function Mutations Causative for Lung Disease.
Prapa M, Lago-Docampo M, Swietlik EM, Montani D, Eyries M, Humbert M, Welch CL, Chung WK, Berger RMF, Bogaard HJ, Danhaive O, Escribano-Subías P, Gall H, Girerd B, Hernandez-Gonzalez I, Holden S, Hunt D, Jansen SMA, Kerstjens-Frederikse W, Kiely DG, Lapunzina P, McDermott J, Moledina S, Pepke-Zaba J, Polwarth GJ, Schotte G, Tenorio-Castaño J, Thompson AAR, Wharton J, Wort SJ, Megy K, Mapeta R, Treacy CM, Martin JM, Li W, Swift AJ, Upton PD, Morrell NW, Gräf S, Valverde D; NIHR BioResource for Translational Research–Rare Diseases; National Cohort Study of Idiopathic and Heritable PAH; PAH Biobank Enrolling Centers’ Investigators. Prapa M, et al. Among authors: danhaive o. Am J Respir Crit Care Med. 2022 Dec 15;206(12):1522-1533. doi: 10.1164/rccm.202203-0485OC. Am J Respir Crit Care Med. 2022. PMID: 35852389 Free PMC article.
Hypothermia and Meconium Aspiration Syndrome: International Multicenter Retrospective Cohort Study.
De Luca D, Tingay DG, van Kaam A, Brunow de Carvalho W, Valverde E, Christoph Roehr C, Mosca F, Matassa PG, Danhaive O, Carnielli VP, Piastra M; IGLOO Study Group. De Luca D, et al. Among authors: danhaive o. Am J Respir Crit Care Med. 2016 Aug 1;194(3):381-4. doi: 10.1164/rccm.201602-0422LE. Am J Respir Crit Care Med. 2016. PMID: 27479063 No abstract available.
Reply to Giesinger and McNamara: The Impact of Therapeutic Hypothermia on Pulmonary Hemodynamics of Meconium Aspiration Syndrome.
De Luca D, Tingay DG, van Kaam A, Brunow de Carvalho W, Valverde E, Roehr CC, Mosca F, Matassa PG, Danhaive O, Carnielli VP, Piastra M; IGLOO Study Group. De Luca D, et al. Among authors: danhaive o. Am J Respir Crit Care Med. 2018 Jul 15;198(2):287-288. doi: 10.1164/rccm.201803-0411LE. Am J Respir Crit Care Med. 2018. PMID: 29590532 No abstract available.
Phenotype characterisation of TBX4 mutation and deletion carriers with neonatal and paediatric pulmonary hypertension.
Galambos C, Mullen MP, Shieh JT, Schwerk N, Kielt MJ, Ullmann N, Boldrini R, Stucin-Gantar I, Haass C, Bansal M, Agrawal PB, Johnson J, Peca D, Surace C, Cutrera R, Pauciulo MW, Nichols WC, Griese M, Ivy D, Abman SH, Austin ED, Danhaive O. Galambos C, et al. Among authors: danhaive o. Eur Respir J. 2019 Aug 22;54(2):1801965. doi: 10.1183/13993003.01965-2018. Print 2019 Aug. Eur Respir J. 2019. PMID: 31151956 Free article.
The Montreux definition of neonatal ARDS: biological and clinical background behind the description of a new entity.
De Luca D, van Kaam AH, Tingay DG, Courtney SE, Danhaive O, Carnielli VP, Zimmermann LJ, Kneyber MCJ, Tissieres P, Brierley J, Conti G, Pillow JJ, Rimensberger PC. De Luca D, et al. Among authors: danhaive o. Lancet Respir Med. 2017 Aug;5(8):657-666. doi: 10.1016/S2213-2600(17)30214-X. Epub 2017 Jul 4. Lancet Respir Med. 2017. PMID: 28687343
Pulmonary Hypertension in Developmental Lung Diseases.
Danhaive O, Galambos C, Lakshminrusimha S, Abman SH. Danhaive O, et al. Clin Perinatol. 2024 Mar;51(1):217-235. doi: 10.1016/j.clp.2023.12.001. Epub 2023 Dec 28. Clin Perinatol. 2024. PMID: 38325943 Review.
Clinical and ultrastructural spectrum of diffuse lung disease associated with surfactant protein C mutations.
Peca D, Boldrini R, Johannson J, Shieh JT, Citti A, Petrini S, Salerno T, Cazzato S, Testa R, Messina F, Onofri A, Cenacchi G, Westermark P, Ullmann N, Cogo P, Cutrera R, Danhaive O. Peca D, et al. Among authors: danhaive o. Eur J Hum Genet. 2015 Aug;23(8):1033-41. doi: 10.1038/ejhg.2015.45. Epub 2015 Mar 18. Eur J Hum Genet. 2015. PMID: 25782673 Free PMC article.
65 results