Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Charlotte, Bendixen"'
Autor:
Felicitas Schulz, Ekkehart Jenetzky, Nadine Zwink, Charlotte Bendixen, Florian Kipfmueller, Neysan Rafat, Andreas Heydweiller, Lucas Wessel, Heiko Reutter, Andreas Mueller, Thomas Schaible
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-8 (2021)
Abstract Background Evidence for periconceptional or prenatal environmental risk factors for the development of congenital diaphragmatic hernia (CDH) is still scarce. Here, in a case-control study we investigated potential environmental risk factors
Externí odkaz:
https://doaj.org/article/8f5f3fdfac5c4967aecc5710413a8ed6
Autor:
Erwin Brosens, Nina C. J. Peters, Kim S. van Weelden, Charlotte Bendixen, Rutger W. W. Brouwer, Frank Sleutels, Hennie T. Bruggenwirth, Wilfred F. J. van Ijcken, Danielle C. M. Veenma, Suzan C. M. Cochius-Den Otter, Rene M. H. Wijnen, Alex J. Eggink, Marieke F. van Dooren, Heiko Martin Reutter, Robbert J. Rottier, J. Marco Schnater, Dick Tibboel, Annelies de Klein
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2022)
Congenital diaphragmatic hernia (CDH) is a congenital structural anomaly in which the diaphragm has not developed properly. It may occur either as an isolated anomaly or with additional anomalies. It is thought to be a multifactorial disease in which
Externí odkaz:
https://doaj.org/article/af7137285f524b758a0191a77d8686a3
Autor:
Corina E. Thiem, Jil D. Stegmann, Alina C. Hilger, Lea Waffenschmidt, Charlotte Bendixen, Ricarda Köllges, Eberhard Schmiedeke, Frank‐Mattias Schäfer, Martin Lacher, Ferdinand Kosch, Sabine Grasshoff‐Derr, Carmen Kabs, Jörg Neser, Ekkehart Jenetzky, Julia Fazaal, Johannes Schumacher, Julia Hoefele, Kerstin U. Ludwig, Heiko Reutter
Publikováno v:
Birth Defects Research. 114:478-486
Publikováno v:
European Journal of Pediatric Surgery. 31:472-481
Congenital diaphragmatic hernia (CDH) is a relatively common and severe birth defect with variable clinical outcome and associated malformations in up to 60% of patients. Mortality and morbidity remain high despite advances in pre-, intra-, and postn
Autor:
Julia Fabian, Gabriel C. Dworschak, Lea Waffenschmidt, Luca Schierbaum, Charlotte Bendixen, Stefanie Heilmann-Heimbach, Sugirthan Sivalingam, Andreas Buness, Nicole Schwarzer, Thomas M. Boemers, Eberhard Schmiedeke, Jörg Neser, Johannes Leonhardt, Ferdinand Kosch, Sandra Weih, Helen Maya Gielen, Stuart Hosie, Carmen Kabs, Markus Palta, Stefanie Märzheuser, Lena Marie Bode, Martin Lacher, Frank-Mattias Schäfer, Maximilian Stehr, Christian Knorr, Benno Ure, Katharina Kleine, Udo Rolle, Marcin Zaniew, Grote Phillip, Nadine Zwink, Ekkehart Jenetzky, Heiko Reutter, Alina C. Hilger
Publikováno v:
European journal of human genetics : EJHG. 31(1)
Anorectal malformations (ARM) represent a spectrum of rare malformations originating from a perturbated development of the embryonic hindgut. Approximately 60% occur as a part of a defined genetic syndrome or within the spectrum of additional congeni
Autor:
Corina E, Thiem, Jil D, Stegmann, Alina C, Hilger, Lea, Waffenschmidt, Charlotte, Bendixen, Ricarda, Köllges, Eberhard, Schmiedeke, Frank-Mattias, Schäfer, Martin, Lacher, Ferdinand, Kosch, Sabine, Grasshoff-Derr, Carmen, Kabs, Jörg, Neser, Ekkehart, Jenetzky, Julia, Fazaal, Johannes, Schumacher, Julia, Hoefele, Kerstin U, Ludwig, Heiko, Reutter
Publikováno v:
Birth defects researchREFERENCES. 114(10)
The acronym VATER/VACTERL association describes the combination of at least three component features (CFs): vertebral defects (V), anorectal malformations (ARM) (A), cardiac defects (C), tracheoesophageal fistula with or without esophageal atresia (T
Autor:
Erwin Brosens, Nina C. J. Peters, Kim S. van Weelden, Charlotte Bendixen, Rutger W. W. Brouwer, Frank Sleutels, Hennie T. Bruggenwirth, Wilfred F. J. van Ijcken, Danielle C. M. Veenma, Suzan C. M. Cochius-Den Otter, Rene M. H. Wijnen, Alex J. Eggink, Marieke F. van Dooren, Heiko Martin Reutter, Robbert J. Rottier, J. Marco Schnater, Dick Tibboel, Annelies de Klein
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2022)
Congenital diaphragmatic hernia (CDH) is a congenital structural anomaly in which the diaphragm has not developed properly. It may occur either as an isolated anomaly or with additional anomalies. It is thought to be a multifactorial disease in which
Autor:
Charlotte Bendixen, Heiko Reutter
Publikováno v:
Genes
Genes, Vol 12, Iss 1405, p 1405 (2021)
Genes, Vol 12, Iss 1405, p 1405 (2021)
The genetic etiology of congenital diaphragmatic hernia (CDH), a common and severe birth defect, is still incompletely understood. Chromosomal aneuploidies, copy number variations (CNVs), and variants in a large panel of CDH-associated genes, both de
Autor:
Andreas Müller, Andreas Heydweiller, Tamene Melaku, Florian Kipfmueller, Heiko Reutter, Annegret Geipel, Christoph Berg, Charlotte Bendixen, Ulrich Gembruch, Lukas Schroeder
Publikováno v:
Klinische Padiatrie. 231(6)
The mortality of neonates with congenital diaphragmatic hernia (CDH) ranges between 20 and 40% even in specialized high-volume centers. The Score for Neonatal Acute Physiology-II (SNAP-II Score) could facilitate the decision about supportive therapie
Autor:
Emma Adams, Pär Gabrielsson, Milica Folic, Per-Anders Carlsson, Magnus Skoglundh, Eva Charlotte Bendixen
Publikováno v:
Applied Catalysis B: Environmental. 165:10-19
We report experimental results for the formation of ammonia from nitric oxide and hydrogen, and from nitric oxide, water and carbon monoxide over silica, alumina and titania supported platinum and palladium catalysts. Temperature programmed reaction