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Year Number of Results
1990 1
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2012 3
2013 3
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2016 3
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2021 6
2022 4
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42 results

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Page 1
Randomized Trial of Fetal Surgery for Severe Left Diaphragmatic Hernia.
Deprest JA, Nicolaides KH, Benachi A, Gratacos E, Ryan G, Persico N, Sago H, Johnson A, Wielgoś M, Berg C, Van Calster B, Russo FM; TOTAL Trial for Severe Hypoplasia Investigators. Deprest JA, et al. N Engl J Med. 2021 Jul 8;385(2):107-118. doi: 10.1056/NEJMoa2027030. Epub 2021 Jun 8. N Engl J Med. 2021. PMID: 34106556 Free PMC article. Clinical Trial.
Randomized Trial of Fetal Surgery for Moderate Left Diaphragmatic Hernia.
Deprest JA, Benachi A, Gratacos E, Nicolaides KH, Berg C, Persico N, Belfort M, Gardener GJ, Ville Y, Johnson A, Morini F, Wielgoś M, Van Calster B, DeKoninck PLJ; TOTAL Trial for Moderate Hypoplasia Investigators. Deprest JA, et al. N Engl J Med. 2021 Jul 8;385(2):119-129. doi: 10.1056/NEJMoa2026983. Epub 2021 Jun 8. N Engl J Med. 2021. PMID: 34106555 Free PMC article. Clinical Trial.
Trio Exome Sequencing in VACTERL Association.
Ćomić J, Tilch E, Riedhammer KM, Brugger M, Brunet T, Eyring K, Vill K, Redler S, Tasic V, Schmiedeke E, Schäfer FM, Abazi-Emini N, Jenetzky E, Schwarzer N, Widenmann A, Lacher M, Zech M, Grasshoff-Derr S, Geßner M, Kabs C, Seitz B, Heydweiller AC, Muensterer O, Lange-Sperandio B, Rolle U, Schumacher J, Braunisch MC, Berutti R, Reutter H, Hoefele J. Ćomić J, et al. Among authors: heydweiller ac. Kidney Int Rep. 2024 Dec 9;10(3):877-891. doi: 10.1016/j.ekir.2024.12.006. eCollection 2025 Mar. Kidney Int Rep. 2024. PMID: 40225364 Free PMC article.
Common variants increase risk for congenital diaphragmatic hernia within the context of de novo variants.
Qiao L, Welch CL, Hernan R, Wynn J, Krishnan US, Zalieckas JM, Buchmiller T, Khlevner J, De A, Farkouh-Karoleski C, Wagner AJ, Heydweiller A, Mueller AC, de Klein A, Warner BW, Maj C, Chung D, McCulley DJ, Schindel D, Potoka D, Fialkowski E, Schulz F, Kipfmuller F, Lim FY, Magielsen F, Mychaliska GB, Aspelund G, Reutter HM, Needelman H, Schnater JM, Fisher JC, Azarow K, Elfiky M, Nöthen MM, Danko ME, Li M, Kosiński P, Wijnen RMH, Cusick RA, Soffer SZ, Cochius-Den Otter SCM, Schaible T, Crombleholme T, Duron VP, Donahoe PK, Sun X, High FA, Bendixen C, Brosens E, Shen Y, Chung WK. Qiao L, et al. Among authors: heydweiller a. Am J Hum Genet. 2024 Nov 7;111(11):2362-2381. doi: 10.1016/j.ajhg.2024.08.024. Epub 2024 Sep 26. Am J Hum Genet. 2024. PMID: 39332409 Free PMC article.
Nine new twin pairs with esophageal atresia: a review of the literature and performance of a twin study of the disorder.
Schulz AC, Bartels E, Stressig R, Ritgen J, Schmiedeke E, Mattheisen M, Draaken M, Ludwig M, Bagci S, Müller A, Gembruch U, Geipel A, Berg C, Heydweiller A, Bachour H, Schumacher J, Bartmann P, Nöthen MM, Reutter H. Schulz AC, et al. Among authors: heydweiller a. Birth Defects Res A Clin Mol Teratol. 2012 Mar;94(3):182-6. doi: 10.1002/bdra.22879. Epub 2012 Jan 30. Birth Defects Res A Clin Mol Teratol. 2012. PMID: 22287212
Rapunzel's Syndrome--a rare phenomenon.
Rickert AT, Düker G, Heydweiller A, Strohm J, Born M, Franke I. Rickert AT, et al. Among authors: heydweiller a. Klin Padiatr. 2014 Sep;226(5):297-8. doi: 10.1055/s-0034-1385867. Epub 2014 Aug 25. Klin Padiatr. 2014. PMID: 25153914 No abstract available.
Defining Excellence: The First Core Set of Quality Indicators for the European Paediatric Surgical Audit on Hirschsprung's Disease Care.
Rossi D, Granström AL, Pakarinen M, Bjørnland K, de Blaauw I, Ellebæk M, Leon FF, Gloudemans DJ, Prato AP, Rolle U, Schwarzer N, Tabbers M, Vilanova A, Wijnen R, Sloots CEJ, Wester T; EPSA|ERNICA Registry Group and collaborative authors. Rossi D, et al. Acta Paediatr. 2025 Jun;114(6):1464-1477. doi: 10.1111/apa.17594. Epub 2025 Jan 25. Acta Paediatr. 2025. PMID: 39865350 Free PMC article.
42 results