Zobrazeno 1 - 10
of 379
pro vyhledávání: '"H. Wijnen"'
Autor:
G. G. Edel, M. van Kempen, A. Boerema-de Munck, C. N. Huisman, C. A. P. Naalden, R. W. W. Brouwer, S. Koornneef, W. F. J. van IJcken, R. M. H. Wijnen, R. J. Rottier
Publikováno v:
Journal of Biomedical Science, Vol 31, Iss 1, Pp 1-17 (2024)
Abstract Background Alveolar capillary dysplasia with misalignment of pulmonary veins (ACD/MPV) is a fatal congenital lung disorder strongly associated with genomic alterations in the Forkhead box F1 (FOXF1) gene and its regulatory region. However, l
Externí odkaz:
https://doaj.org/article/64a93163d0b443069e918dece0926290
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:
Suzanne Polinder, Detlef van der Velde, Taco Gosens, Esther M M van Lieshout, Michael H J Verhofstad, Pieter Joosse, K de Vries, Dennis Den Hartog, J. Jansen, Ruth E Pel-Littel, Henk Jan Schuijt, Miliaan L Zeelenberg, Paulieke C Oosterwijk, Hanna C Willems, Sverre A I Loggers, Thomas MP Nijdam, Hugo H Wijnen, E. Sohl, J.A. Jansen, M. Leijnen, W.A.H. Van der Stappen, M Peters-Kop, A.H. Van der Veen, N.C. Schepel, J.A.M. Wilmer, J. Steens, J. Winkelhagen, N.M.F. Noorda, H.A.A.M. Maas, O. Wijers, V. Vis, D. Van der Stap, G.R. Roukema, E. Bosma, T.M. Van Raaij, A.M. Van der Knaap, R. De Groot, A.V.C.M. Zeegers, H.A. Formijne Jonkers, D.H.R. Kempen, A.F Pull ter Gunne, M.P. Somford, E. Tanis, J.H. Duits, R.A. Zandbergen, N.C. Leegwater, O.C. Geraghty, J.H. Hegeman, E.M. Regtuijt
Publikováno v:
BMJ Open, Vol 14, Iss 4 (2024)
Background and purpose Recent research has highlighted non-operative management (NOM) as a viable alternative for frail older adults with hip fractures in the final phase of life. This study aims to guide Dutch physicians and hospitals nationwide in
Externí odkaz:
https://doaj.org/article/3edb7ca2aba14272bf955bbb67838815
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:
Hugo H Wijnen, Peter P Schmitz, Houda Es-Safraouy, Lian A Roovers, Diana G Taekema, Job L C Van Susante
Publikováno v:
Acta Orthopaedica, Vol 92, Iss 6, Pp 728-732 (2021)
Background and purpose — Surgical treatment is still the mainstay of care even in very frail elderly hip fracture patients. However, one may argue whether surgery is in the best interest of all patients. We elucidated mortality rates of nonoperativ
Externí odkaz:
https://doaj.org/article/98c6eb937f8442a18f3b9833f62b226c
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