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Browsing by Author "Blaauw, I. de"
Now showing items 1-50 of 80
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Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformations Putte, R. van de; ; Reutter, H.; ; ; Brosens, E.; Broens, P.; Homberg, M.; Ludwig, M.; Jenetzky, E.; et al.2019, Article / Letter to editor (PLoS One, vol. 14, iss. 5, (2019), article e0217477)
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The Pediatric Colorectal and Pelvic Learning Consortium (PCPLC): rationale, infrastructure, and initial steps Reeder, R.W.; Wood, R.J.; Avansino, J.R.; Levitt, M.A.; Durham, M.M.; Sutcliffe, J.; Midrio, P.; Calkins, C.M.; ; Dickie, B.H.; et al.2018, Article / Letter to editor (Techniques in Coloproctology, vol. 22, iss. 5, (2018), pp. 395-399)
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The timing of surgery of antenatally diagnosed choledochal malformations: A descriptive analysis of a 26-year nationwide cohort Eijnden, M.H.A. van den; Kleine, R.H. de; ; Peeters, P.; Koot, B.G.; Oomen, M.W.A.T.; Sloots, C.E.; Gemert, W.G. van; Zee, D.C. van der; Heurn, L.W. van; et al.2017, Article / Letter to editor (Journal of Pediatric Surgery, vol. 52, iss. 7, (2017), pp. 1156-1160)
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Choledochal Malformation in Children: Lessons Learned from a Dutch National Study Eijnden, M.H.A. van den; Kleine, R.H. de; ; Peeters, P.; Koot, B.P.G.; Oomen, M.W.A.T.; Sloots, C.E.; Gemert, W.G. van; Zee, D.C. van der; Heurn, L.W. van; et al.2017, Article / Letter to editor (World Journal of Surgery, vol. 41, iss. 10, (2017), pp. 2631-2637)
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Tethered cord in patients affected by anorectal malformations: a survey from the ARM-Net Consortium Fanjul, M.; Samuk, I.; Bagolan, P.; Leva, E.; Sloots, C.; Gine, C.; Aminoff, D.; Midrio, P.; ; ; et al.2017, Article / Letter to editor (Pediatric Surgery International, vol. 33, iss. 8, (2017), pp. 849-854)
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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.; Klein, A.; Ijsselstijn, H.; ; ; ; Broens, P.M.; ; et al.2016, Article / Letter to editor (European Journal of Pediatrics, vol. 175, iss. 6, (2016), pp. 825-831)
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AGORA, a data- and biobank for birth defects and childhood cancer ; ; ; ; Wijers, C.H.; Thonissen, M.; Dokter, E.M.; ; ; ; et al.2016, Article / Letter to editor (Birth Defects Research Part A-Clinical and Molecular Teratology, vol. 106, iss. 8, (2016), pp. 675-684)
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Children With Anorectal Malformations, Hirschsprung Disease, and Their Siblings: Proxy Reports and Self-Reports Hartman, E.E.; Oort, F.J.; ; Steeg, A.F. van der; Heij, H.A.; Heurn, E. van; Madern, G.C.; Zee, D.C. van der; ; Dijk, A. van; et al.2015, Article / Letter to editor (Journal of Pediatric Gastroenterology and Nutrition, vol. 61, iss. 6, (2015), pp. 630-635)
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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.; ; Lacher, M.; Grasshoff-Derr, S.; Garcia-Vazquez, A.; Giuliani, S.; Midrio, P.; Gamba, P.; Iacobelli, B.; Bagolan, P.; et al.2015, Article / Letter to editor (Pediatric Surgery International, vol. 31, iss. 8, (2015), pp. 741-745)
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European consensus meeting of ARM-Net members concerning diagnosis and early management of newborns with anorectal malformations Steeg, H.J.J. van der; Schmiedeke, E.; Bagolan, P.; Broens, P.; Demirogullari, B.; Garcia-Vazquez, A.; Grasshoff-Derr, S.; Lacher, M.; Leva, E.; Makedonsky, I.; et al.2015, Article / Letter to editor (Techniques in Coloproctology, vol. 19, iss. 3, (2015), pp. 181-185)
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Sequencing of the DKK1 gene in patients with anorectal malformations and hypospadias Putte, R. van de; ; ; ; ; Hakobjan, M.H.; Sloots, C.E.; Bever, Y. Van; ; ; et al.2015, Article / Letter to editor (European Journal of Pediatrics, vol. 174, iss. 5, (2015), pp. 583-587)
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Clinical outcome of cloacal exstrophy, current status, and a change in surgical management Vliet, R.; ; Rassouli, R.; ; ; ; ; ; ; ; et al.2015, Article / Letter to editor (European Journal of Pediatric Surgery, vol. 25, iss. 1, (2015), pp. 87-93)
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Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association Saisawat, P.; Kohl, S.; Hilger, A.C.; Hwang, D.Y.; Yung Gee, H.; Dworschak, G.C.; Tasic, V.; Pennimpede, T.; Natarajan, S.; Sperry, E.; et al.2014, Article / Letter to editor (Kidney International. Supplement, vol. 85, iss. 6, (2014), pp. 1310-1317)
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Now showing items 1-50 of 80
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