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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1987 2
1988 2
1990 4
1992 1
1993 2
1995 3
1997 2
1999 1
2000 5
2001 2
2004 3
2005 2
2006 1
2007 2
2009 1
2010 3
2011 9
2012 9
2013 9
2014 5
2015 3
2016 4
2017 9
2018 7
2019 9
2020 4
2021 11
2022 13
2023 10
2024 6

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128 results

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Page 1
Trisomy 13 and 18-Prevalence and mortality-A multi-registry population based analysis.
Goel N, Morris JK, Tucker D, de Walle HEK, Bakker MK, Kancherla V, Marengo L, Canfield MA, Kallen K, Lelong N, Camelo JL, Stallings EB, Jones AM, Nance A, Huynh MP, Martínez-Fernández ML, Sipek A, Pierini A, Nembhard WN, Goetz D, Rissmann A, Groisman B, Luna-Muñoz L, Szabova E, Lapchenko S, Zarante I, Hurtado-Villa P, Martinez LE, Tagliabue G, Landau D, Gatt M, Dastgiri S, Morgan M. Goel N, et al. Among authors: lelong n. Am J Med Genet A. 2019 Dec;179(12):2382-2392. doi: 10.1002/ajmg.a.61365. Epub 2019 Sep 30. Am J Med Genet A. 2019. PMID: 31566869 Free PMC article.
Ten-year survival of children with trisomy 13 or trisomy 18: a multi-registry European cohort study.
Glinianaia SV, Rankin J, Tan J, Loane M, Garne E, Cavero-Carbonell C, de Walle HEK, Gatt M, Gissler M, Klungsøyr K, Lelong N, Neville A, Pierini A, Tucker DF, Urhoj SK, Wellesley DG, Morris JK. Glinianaia SV, et al. Among authors: lelong n. Arch Dis Child. 2023 Jun;108(6):461-467. doi: 10.1136/archdischild-2022-325068. Epub 2023 Mar 7. Arch Dis Child. 2023. PMID: 36882305
Surveillance of multiple congenital anomalies; searching for new associations.
Morris JK, Bergman JEH, Barisic I, Wellesley D, Tucker D, Limb E, Addor MC, Cavero-Carbonell C, Matias Dias C, Draper ES, Echevarría-González-de-Garibay LJ, Gatt M, Klungsøyr K, Lelong N, Luyt K, Materna-Kiryluk A, Nelen V, Neville A, Perthus I, Pierini A, Randrianaivo-Ranjatoelina H, Rankin J, Rissmann A, Rouget F, Sayers G, Wertelecki W, Kinsner-Ovaskainen A, Garne E. Morris JK, et al. Among authors: lelong n. Eur J Hum Genet. 2024 Apr;32(4):407-412. doi: 10.1038/s41431-023-01502-w. Epub 2023 Dec 5. Eur J Hum Genet. 2024. PMID: 38052905 Free PMC article. Review.
Epidemiology of achondroplasia: A population-based study in Europe.
Coi A, Santoro M, Garne E, Pierini A, Addor MC, Alessandri JL, Bergman JEH, Bianchi F, Boban L, Braz P, Cavero-Carbonell C, Gatt M, Haeusler M, Klungsøyr K, Kurinczuk JJ, Lanzoni M, Lelong N, Luyt K, Mokoroa O, Mullaney C, Nelen V, Neville AJ, O'Mahony MT, Perthus I, Rankin J, Rissmann A, Rouget F, Schaub B, Tucker D, Wellesley D, Wisniewska K, Zymak-Zakutnia N, Barišić I. Coi A, et al. Among authors: lelong n. Am J Med Genet A. 2019 Sep;179(9):1791-1798. doi: 10.1002/ajmg.a.61289. Epub 2019 Jul 11. Am J Med Genet A. 2019. PMID: 31294928
[Familial violence during pregnancy].
Saurel-Cubizolles MJ, Lelong N. Saurel-Cubizolles MJ, et al. Among authors: lelong n. J Gynecol Obstet Biol Reprod (Paris). 2005 Feb;34(1 Suppl):S47-53. doi: 10.1016/s0368-2315(05)82687-0. J Gynecol Obstet Biol Reprod (Paris). 2005. PMID: 15767931 Free article. Review. French.
Quality of Life of Children Born with a Congenital Heart Defect.
Derridj N, Bonnet D, Calderon J, Amedro P, Bertille N, Lelong N, Goffinet F, Khoshnood B, Guedj R. Derridj N, et al. Among authors: lelong n. J Pediatr. 2022 May;244:148-153.e5. doi: 10.1016/j.jpeds.2022.01.003. Epub 2022 Jan 13. J Pediatr. 2022. PMID: 35033563
Ten-Year Survival of Children With Congenital Anomalies: A European Cohort Study.
Glinianaia SV, Rankin J, Pierini A, Coi A, Santoro M, Tan J, Reid A, Garne E, Loane M, Given J, Cavero-Carbonell C, de Walle HEK, Gatt M, Gissler M, Heino A, Khoshnood B, Klungsøyr K, Lelong N, Neville AJ, Thayer DS, Tucker D, Urhøj SK, Wellesley D, Zurriaga O, Morris JK. Glinianaia SV, et al. Among authors: lelong n. Pediatrics. 2022 Mar 1;149(3):e2021053793. doi: 10.1542/peds.2021-053793. Pediatrics. 2022. PMID: 35146505
128 results