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Towards the perfect ARM center: the European Union's criteria for centers of expertise and their implementation in the member states. A report from the ARM-Net.
Schmiedeke E, de Blaauw I, Lacher M, Grasshoff-Derr S, Garcia-Vazquez A, Giuliani S, Midrio P, Gamba P, Iacobelli B, Bagolan P, Brisighelli G, Leva E, Cretolle C, Sarnacki S, Broens P, Sloots C, van Rooij I, Schwarzer N, Aminoff D, Haanen M, Jenetzky E. Schmiedeke E, et al. Among authors: lacher m. Pediatr Surg Int. 2015 Aug;31(8):741-5. doi: 10.1007/s00383-015-3752-6. Epub 2015 Jul 26. Pediatr Surg Int. 2015. PMID: 26210660
Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomalies.
Zeidler C, Woelfle J, Draaken M, Mughal SS, Große G, Hilger AC, Dworschak GC, Boemers TM, Jenetzky E, Zwink N, Lacher M, Schmidt D, Schmiedeke E, Grasshoff-Derr S, Märzheuser S, Holland-Cunz S, Schäfer M, Bartels E, Keppler K, Palta M, Leonhardt J, Kujath C, Rißmann A, Nöthen MM, Reutter H, Ludwig M. Zeidler C, et al. Among authors: lacher m. Birth Defects Res A Clin Mol Teratol. 2014 Oct;100(10):750-9. doi: 10.1002/bdra.23278. Epub 2014 Aug 8. Birth Defects Res A Clin Mol Teratol. 2014. PMID: 25131394
Genome-wide mapping of copy number variations in patients with both anorectal malformations and central nervous system abnormalities.
Dworschak GC, Draaken M, Hilger AC, Schramm C, Bartels E, Schmiedeke E, Grasshoff-Derr S, Märzheuser S, Holland-Cunz S, Lacher M, Jenetzky E, Zwink N, Schmidt D, Nöthen MM, Ludwig M, Reutter H. Dworschak GC, et al. Among authors: lacher m. Birth Defects Res A Clin Mol Teratol. 2015 Apr;103(4):235-42. doi: 10.1002/bdra.23321. Epub 2014 Sep 24. Birth Defects Res A Clin Mol Teratol. 2015. PMID: 25250690
European consensus meeting of ARM-Net members concerning diagnosis and early management of newborns with anorectal malformations.
van der Steeg HJ, Schmiedeke E, Bagolan P, Broens P, Demirogullari B, Garcia-Vazquez A, Grasshoff-Derr S, Lacher M, Leva E, Makedonsky I, Sloots CE, Schwarzer N, Aminoff D, Schipper M, Jenetzky E, van Rooij IA, Giuliani S, Crétolle C, Holland Cunz S, Midrio P, de Blaauw I. van der Steeg HJ, et al. Among authors: lacher m. Tech Coloproctol. 2015 Mar;19(3):181-5. doi: 10.1007/s10151-015-1267-8. Epub 2015 Jan 22. Tech Coloproctol. 2015. PMID: 25609592 Free PMC article.
Comparison of environmental risk factors for esophageal atresia, anorectal malformations, and the combined phenotype in 263 German families.
Zwink N, Choinitzki V, Baudisch F, Hölscher A, Boemers TM, Turial S, Kurz R, Heydweiller A, Keppler K, Müller A, Bagci S, Pauly M, Brokmeier U, Leutner A, Degenhardt P, Schmiedeke E, Märzheuser S, Grasshoff-Derr S, Holland-Cunz S, Palta M, Schäfer M, Ure BM, Lacher M, Nöthen MM, Schumacher J, Jenetzky E, Reutter H. Zwink N, et al. Among authors: lacher m. Dis Esophagus. 2016 Nov;29(8):1032-1042. doi: 10.1111/dote.12431. Epub 2015 Nov 6. Dis Esophagus. 2016. PMID: 26541887
More than fetal urine: enteral uptake of amniotic fluid as a major predictor for fetal growth during late gestation.
Bagci S, Brosens E, Tibboel D, De Klein A, Ijsselstijn H, Wijers CH, Roeleveld N, de Blaauw I, Broens PM, van Rooij IA, Hölscher A, Boemers TM, Pauly M, Münsterer OJ, Schmiedeke E, Schäfer M, Ure BE, Lacher M, Choinitzki V, Schumacher J, Zwink N, Jenetzky E, Katzer D, Arand J, Bartmann P, Reutter HM. Bagci S, et al. Among authors: lacher m. Eur J Pediatr. 2016 Jun;175(6):825-31. doi: 10.1007/s00431-016-2713-y. Epub 2016 Mar 16. Eur J Pediatr. 2016. PMID: 26979529
Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations.
Zhang R, Marsch F, Kause F, Degenhardt F, Schmiedeke E, Märzheuser S, Hoppe B, Bachour H, Boemers TM, Schäfer M, Spychalski N, Neser J, Leonhardt J, Kosch F, Ure B, Gómez B, Lacher M, Deffaa OJ, Palta M, Wittekindt B, Kleine K, Schmedding A, Grasshoff-Derr S, Ven AV, Heilmann-Heimbach S, Zwink N, Jenetzky E, Ludwig M, Reutter H. Zhang R, et al. Among authors: lacher m. Birth Defects Res. 2017 Jul 17;109(13):1063-1069. doi: 10.1002/bdr2.1042. Epub 2017 Jun 12. Birth Defects Res. 2017. PMID: 28605140
255 results