Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Nynke J. Elzenga"'
Autor:
Adriana C Gittenberger-de Groot, Joshua C Peterson, Lambertus J Wisse, Arno A W Roest, Robert E Poelmann, Regina Bökenkamp, Nynke J Elzenga, Mark Hazekamp, Margot M Bartelings, Monique R M Jongbloed, Marco C DeRuiter
Publikováno v:
PLoS ONE, Vol 15, Iss 5, p e0228478 (2020)
OBJECTIVES:In congenital heart malformations with pulmonary stenosis to atresia an abnormal lateral ductus arteriosus to left pulmonary artery connection can lead to a localised narrowing (pulmonary ductal coarctation) or even interruption We investi
Externí odkaz:
https://doaj.org/article/97d995e43a3340e7b428c696ec3085d5
Autor:
Lambertus J. Wisse, Marco C. DeRuiter, Monique R.M. Jongbloed, Joshua C. Peterson, Margot M. Bartelings, Adriana C. Gittenberger-de Groot, Nynke J. Elzenga, Robert E. Poelmann, Regina Bökenkamp, Arno A.W. Roest, Mark G. Hazekamp
Publikováno v:
PLoS ONE
PLoS ONE, Vol 15, Iss 5, p e0228478 (2020)
PLoS ONE, 15(5), e0228478
PLoS ONE, 15(5). PUBLIC LIBRARY SCIENCE
PLoS ONE, Vol 15, Iss 5, p e0228478 (2020)
PLoS ONE, 15(5), e0228478
PLoS ONE, 15(5). PUBLIC LIBRARY SCIENCE
Background In a normal neonatal heart the ductus arteriosus forms the direct continuity of the pulmonary trunk to the descending aorta being the main channel for the prenatal blood flow. The pulmonary arteries originate separately from the pulmonary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65a3b4c7191c5bbd2cc304f93853c58d
https://hdl.handle.net/1887/3181313
https://hdl.handle.net/1887/3181313
Autor:
Paul M. A. Broens, Nynke J. Elzenga, Jara E. Jonker, Bouwe Molenbuur, Monika Trzpis, Eryn T. Liem
Publikováno v:
The Journal of Pediatrics, 179, 150-153. MOSBY-ELSEVIER
Objective To determine the prevalence of congenital heart defects (CHDs) in patients with mild or severe congenital anorectal malformations (CARMs), and whether all patients with CARM need pediatric cardiology screening.Study design We included 129 p
Autor:
Nynke J. Elzenga, Beatrijs Bartelds, Hans L. Hillege, Dick van de Weerd, Marcus T. R. Roofthooft, Mark-Jan Ploegstra, Rolf M. F. Berger, Johannes M. Douwes
Publikováno v:
Circulation-Cardiovascular Imaging, 8(1), 1-10. LIPPINCOTT WILLIAMS & WILKINS
Background— The value of echocardiography in assessing disease severity and predicting outcome in pediatric pulmonary arterial hypertension (PAH) is insufficiently defined. The aim of this study was to describe correlations between echocardiography
Autor:
Rolf M. F. Berger, Tjark Ebels, Nynke J. Elzenga, Tjalling W. Waterbolk, Ymkje J. van Slooten
Publikováno v:
Annals of thoracic surgery, 93(6), 2022-2027. ELSEVIER SCIENCE INC
Background. Functional univentricular hearts are currently palliated by a staged procedure of which the bidirectional cavopulmonary shunt is usually the second stage. In addition to this stage, a calibrated amount of additional pulmonary blood flow m
Autor:
Annemiek Smit-van Oosten, Nynke J. Elzenga, Bibiche Boersma, Beatrijs Bartelds, Rolf M. F. Berger, Marcel G.J. Nederhoff, Marinus A.J. Borgdorff, Janny Takens, Wiek H. van Gilst, Leon J. De Windt
Publikováno v:
European journal of heart failure, 13(12), 1275-1282. Wiley
European Journal of Heart Failure, 13(12), 1275-1282. Wiley
European Journal of Heart Failure, 13(12), 1275-1282. Wiley
Aims Right ventricular (RV) dysfunction is a major determinant of long-term morbidity and mortality in congenital heart disease. The right ventricle (RV) is genetically different from the left ventricle (LV), but it is unknown as to whether this has
Autor:
Nynke J. Elzenga, Beatrijs Bartelds, Albertus Timmer, Joost P. van Melle, Leanne de Vetten, Klasien A. Bergman
Publikováno v:
Pediatric cardiology, 32(4), 492-497. SPRINGER
We report a 29 week-gestation preterm infant who presented during his second week of life with cardiogenic shock. Clinical presentation and first diagnostics suggested myocardial infarction, but echocardiographic features during follow-up pointed to
Autor:
Tjalling W. Waterbolk, Tjark Ebels, Nynke J. Elzenga, Gertie C. M. Beaufort-Krol, Margreet Th.E. Bink-Boelkens
Publikováno v:
European Journal of Cardio-Thoracic Surgery. 14:590-595
Objective: Total cavopulmonary connection (TCPC) is a routine operation for palliation of children with cardiac anomalies in whom biventricular repair is impossible. The original technique consists of the creation of a semi-prosthetic intercaval tunn
Autor:
Nynke J. Elzenga, Tjark Ebels, Michiel E. Erasmus, Ad J.J.C. Bogers, A Eijgelaar, Adri H. Cromme-Dijkhuis, Caroline Contant, René M.H.J. Brouwer
Publikováno v:
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 111(1), 168-175. MOSBY-ELSEVIER
Coarctation of the aorta and associated ventricular septal defect may be repaired simultaneously or by initial coarctation repair with or without banding of the pulmonary artery. The question is whether specific preoperative criteria can enable the s
Publikováno v:
The Journal of Thoracic and Cardiovascular Surgery. 108:692-699
Now that systemic-pulmonary collateral arteries are used for unifocalization in patients with pulmonary atresia and ventricular septal defect, the question arises whether morphologic criteria of these collateral arteries could help to provide better