Zobrazeno 1 - 10
of 262
pro vyhledávání: '"M H, Wijnen"'
Autor:
Emily J. J. Horn-Oudshoorn, Marijn J. Vermeulen, Ronny Knol, Rebekka Bout-Rebel, Arjan B. te Pas, Stuart B. Hooper, Suzan C. M. Cochius-den Otter, Rene M. H. Wijnen, Kelly J. Crossley, Neysan Rafat, Thomas Schaible, Willem P. de Boode, Anne Debeer, Berndt Urlesberger, Calum T. Roberts, Florian Kipfmueller, Irma Capolupo, Carmen M. Burgos, Bettina E. Hansen, Irwin K. M. Reiss, Philip L. J. DeKoninck
Publikováno v:
Trials, Vol 25, Iss 1, Pp 1-12 (2024)
Abstract Background Infants born with congenital diaphragmatic hernia (CDH) are at high risk of respiratory insufficiency and pulmonary hypertension. Routine practice includes immediate clamping of the umbilical cord and endotracheal intubation. Expe
Externí odkaz:
https://doaj.org/article/b6993f45019b418b959a50622985b099
Autor:
René M H Wijnen, Hanneke IJsselstijn, Joost van Rosmalen, Maarten Schurink, Nagarajan Muthialu, Marten J Poley, J Marco Schnater, Pierluigi Ciet, Harm A W M Tiddens, Paul D Losty, Jan von der Thüsen, Casper M Kersten, Sergei M Hermelijn, Louis W J Dossche, André B Rietman, Tabitha P L Zanen - van den Adel, Erwin Brosens
Publikováno v:
BMJ Open, Vol 13, Iss 3 (2023)
Introduction Consensus is lacking on the optimal management of asymptomatic congenital pulmonary airway malformation (CPAM). For future studies, the CONNECT consortium (the COllaborative Neonatal Network for the first European CPAM Trial)—an intern
Externí odkaz:
https://doaj.org/article/a7f66de3e6e74135aaae85cfcd92f488
Publikováno v:
PLoS ONE, Vol 18, Iss 5, p e0285108 (2023)
In laparoscopic surgery the abdominal cavity is insufflated with pressurized carbon dioxide gas to create workspace. This pressure is exerted through the diaphragm onto the lungs, competing with ventilation and hampering it. In clinical practice the
Externí odkaz:
https://doaj.org/article/142c18095bdb4a64a54751f3b3e1d000
Autor:
Almira Zada, Laura E. Kuil, Bianca M. de Graaf, Naomi Kakiailatu, Jonathan D. Windster, Alice S. Brooks, Marjon van Slegtenhorst, Barbara de Koning, René M. H. Wijnen, Veerle Melotte, Robert M. W. Hofstra, Erwin Brosens, Maria M. Alves
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 10 (2022)
Background: Pediatric Intestinal Pseudo-obstruction (PIPO) is a congenital enteric disorder characterized by severe gastrointestinal (GI) dysmotility, without mechanical obstruction. Although several genes have been described to cause this disease, m
Externí odkaz:
https://doaj.org/article/88f91001bc774e99be4b2759acc6def2
Autor:
Kim A. A. Schilders, Gabriëla G. Edel, Evelien Eenjes, Bianca Oresta, Judith Birkhoff, Anne Boerema-de Munck, Marjon Buscop-van Kempen, Panagiotis Liakopoulos, Petros Kolovos, Jeroen A. A. Demmers, Raymond Poot, Rene M. H. Wijnen, Dick Tibboel, Robbert J. Rottier
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Congenital diaphragmatic hernia is a structural birth defect of the diaphragm, with lung hypoplasia and persistent pulmonary hypertension. Aside from vascular defects, the lungs show a disturbed balance of differentiated airway epithelial cells. The
Externí odkaz:
https://doaj.org/article/2f12adbac68b45d1bf82ee1fe83b5a3e
Autor:
Lotte E. Vlug, Patric J. D. Delhanty, Esther G. Neelis, Martin Huisman, Jenny A. Visser, Edmond H. H. M. Rings, René M. H. Wijnen, Sjoerd C. J. Nagelkerke, Merit M. Tabbers, Jessie M. Hulst, Barbara A. E. de Koning
Publikováno v:
Frontiers in Nutrition, Vol 9 (2022)
BackgroundChildren with intestinal failure (IF) require parenteral nutrition (PN). Transition to oral and enteral nutrition (EN) can be difficult also due to abnormal gastrointestinal motility. The gut hormone ghrelin is increased in states of negati
Externí odkaz:
https://doaj.org/article/3084db30791b44a481ef4d22572d4282
Autor:
Arjan B te Pas, Neysan Rafat, Thomas Schaible, Stuart B Hooper, René M H Wijnen, Kelly J Crossley, Philip L J DeKoninck, Ronny Knol, Irwin K M Reiss, Marijn J Vermeulen, Florian Kipfmueller, Berndt Urlesberger, Anne Debeer, Emily J J Horn-Oudshoorn, Suzan C M Cochius-den Otter, Calum T Roberts, Willem P de Boode
Publikováno v:
BMJ Open, Vol 12, Iss 3 (2022)
Introduction Pulmonary hypertension is a major determinant of postnatal survival in infants with a congenital diaphragmatic hernia (CDH). The current care during the perinatal stabilisation period in these infants might contribute to the development
Externí odkaz:
https://doaj.org/article/ef4b32ffdcf04350902c0dc96af0af5d
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:
Gabriëla G. Edel, Gerben Schaaf, Rene M. H. Wijnen, Dick Tibboel, Gabrielle Kardon, Robbert J. Rottier
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Congenital diaphragmatic hernia (CDH) is a structural birth defect characterized by a diaphragmatic defect, lung hypoplasia and structural vascular defects. In spite of recent developments, the pathogenesis of CDH is still poorly understood. CDH is a
Externí odkaz:
https://doaj.org/article/b1ee41e42cc64e9f89c1c0499fc7b730
Autor:
Sophie de Munck, Monique H. M. van der Cammen-van Zijp, Tabitha P. L. Zanen-van den Adel, René M. H. Wijnen, Suzan C. M. Cochius-den Otter, Neeltje E. M. van Haren, Saskia J. Gischler, Joost van Rosmalen, Hanneke IJsselstijn
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Background and Objectives: Children born with congenital diaphragmatic hernia (CDH) and treated with extracorporeal membrane oxygenation (ECMO), are at risk for motor function impairment during childhood. We hypothesized that all children born with C
Externí odkaz:
https://doaj.org/article/37906b3560fd49279e29c4e7953f03c5