Zobrazeno 1 - 10
of 35
pro vyhledávání: '"J W Roos-Hesselink"'
Autor:
V. P. Zakharova, S. O. Siromakha, J. W. Roos-Hesselink, V. I. Kravchenko, Yu. V. Davydova, V. V. Lazoryshynets
Publikováno v:
Patologìâ, Vol 18, Iss 3, Pp 356-364 (2021)
Aortic dissection is rare but life-threatening complication in pregnancy, causing significant maternal and perinatal losses. Pregnancy may influence the integrity of the vessel wall and is a risk factor for dissection. There are very few data in the
Externí odkaz:
https://doaj.org/article/254c23df910f462caa7e3b54bd8a9fef
Autor:
A. R. Wahadat, W. Tanis, T. W. Galema, L. E. Swart, W. J. van Leeuwen, N. J. Verkaik, C. A. M. Schurink, B. van Dalen, S. Zoet-Nugteren, C. Gurlek, R. P. J. Budde, J. W. Roos-Hesselink
Publikováno v:
Netherlands Heart Journal, 31(1), 29-35. Bohn Stafleu van Loghum
Background In their latest guidelines for infective endocarditis (IE) (2015), the European Society of Cardiology (ESC) introduced the implementation of the Endocarditis Team (ET) to facilitate the management of IE. This study presents our experiences
Autor:
C. Pelosi, R. M. Kauling, J. A. A. E. Cuypers, E. M. W. J. Utens, A. E. van den Bosch, I. Kardys, A. J. J. C. Bogers, W. A. Helbing, J. W. Roos-Hesselink, Jeroen S. Legerstee
Publikováno v:
Clinical Research in Cardiology. D. Steinkopff-Verlag
Background Nowadays, more than 90% of patients with congenital heart disease (CHD) reach adulthood. However, long-term impact on neurodevelopment and executive functioning in adults with CHD are not completely understood. Purpose To investigate the s
Autor:
F. Meccanici, J.W.C. de Bruijn, J.S. Dommisse, J.J.M. Takkenberg, A.E. van den Bosch, J. W. Roos-Hesselink
Women with Turner syndrome (TS) have an increased risk of aortic disease, reducing life-expectancy. This study aimed to systematically review the prevalence of thoracic aortic dilatation, aortic dimensions and growth, and the incidence of aortic diss
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5005a6f86f2b392817ee511b7d0f9e1c
Autor:
C. Pelosi, R. M. Kauling, J. A. A. E. Cuypers, A. E. van den Bosch, W. A. Helbing, E. M. W. J. Utens, J. S. Legerstee, J. W. Roos-Hesselink
Publikováno v:
Clinical Research in Cardiology. D. Steinkopff-Verlag
Introduction Nowadays, more than 90% of patients with congenital heart disease (CHD) reach adulthood. However, knowledge about their psychosocial functioning is limited. Methods Longitudinal cohort study of patients (n = 204, mean age: 50 years, 46.1
Autor:
C Pelosi, R M Kauling, J A A E Cuypers, E M W J Utens, A E Van Den Bosch, I Kardys, A J J C Bogers, W A Helbing, J W Roos-Hesselink, J S Legerstee
Publikováno v:
European Heart Journal. 43
Background For children with congenital heart disease (CHD), subtle neuropsychological deficits have been reported. However, very little is known about executive functioning in their adulthood. Purpose To investigate the self- and informant-reported
Autor:
Z Keuning, F Meccanici, F M Sneep, A Hirsch, J J M Takkenberg, A E Van Den Bosch, J W Roos-Hesselink
Publikováno v:
European Heart Journal. 43
Background Congenital aortic stenosis (ConAoS) accounts for 4–8% of all congenital cardiac diagnosis and is associated with important morbidity and mortality. However, little is known about the natural history of ConAoS in adult patients. We aim to
Publikováno v:
European Heart Journal. 43
Background Ebstein's anomaly is a rare congenital cardiac condition characterized by displacement of the posterior and septal leaflets of the tricuspid valve towards the apex of the right ventricle. The ESC Guidelines for the management of cardiovasc
Autor:
F Meccanici, C G E Thijssen, A L Gokalp, J L De Bruin, J A Bekkers, R R J Van Kimmenade, G S C Geuzebroek, P Poyck, F J Ter Woorst, M C Post, R H Heijmen, M M Mokhles, J J M Takkenberg, J W Roos-Hesselink, H J M Verhagen
Publikováno v:
European Heart Journal. 43
Background/Introduction Acute type B aortic dissection (ATBAD) is a cardiovascular emergency with high risk of morbidity and mortality. Elucidating male-female differences in ATBAD might help optimize patient-specific care, while data is scarce on th
Autor:
K Sliwa-Hahnle, P Van Der Meer, C Viljoen, A M Jackson, M C Petrie, A P Maggioni, C Laroche, V Regitz-Zagrosek, L Tavazzi, J W Roos-Hesselink, P Seferovic, A Frogoudaki, B Ibrahim, H Al-Farham, J Bauersachs
Publikováno v:
European Heart Journal. 43
Background Peripartum cardiomyopathy (PPCM) is a global disease associated with substantial morbidity and mortality. Purpose The aim of this study was to analyse to what extent country- and individual-level socioeconomic factors were associated with