Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Frans van Hoorn"'
Autor:
Frans van Hoorn, Maria E Campian, Anje Spijkerboer, Marieke T Blom, R Nils Planken, Albert C van Rossum, Jacques M T de Bakker, Arthur A M Wilde, Maarten Groenink, Hanno L Tan
Publikováno v:
PLoS ONE, Vol 7, Iss 8, p e42037 (2012)
BACKGROUND: The cardiac sodium channel (Na(v)1.5) controls cardiac excitability. Accordingly, SCN5A mutations that result in loss-of-function of Na(v)1.5 are associated with various inherited arrhythmia syndromes that revolve around reduced cardiac e
Externí odkaz:
https://doaj.org/article/95a4fc16eb9a4957804670757c04603b
Autor:
Frans van Hoorn, Martha Koehn, Rashin F. Rastegar, Elizabeth Roy, Savvas Nicolaou, Ferco H. Berger, Kristy Lee
Publikováno v:
Canadian Association of Radiologists Journal. 63(4):318-322
Autor:
Hans A. Huysmans, Jan A. Bruijn, Mark G. Hazekamp, Robert A.E. Dion, Dave R. Koolbergen, Emile de Heer, Frans van Hoorn
Publikováno v:
European journal of cardio-thoracic surgery, 22(5), 802-807. Elsevier
Objectives: The limited availability of donor valves and experimental evidence that pulmonary valves can withstand systemic pressure made us use cryopreserved pulmonary homografts as aortic valve substitutes. We observed a high incidence of early reo
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 157(49)
A 43-year-old woman came to the Emergency Room with acute abdominal pain during the night. CT examination of the abdomen showed ventral herniation of the stomach and parts of the small intestine and colon in the right hemithorax. We made the diagnosi
Autor:
Maaike, Mühl, Frans, van Hoorn
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 156(12)
A 21-year-old woman reported to the first aid with acute pain in the right lower abdomen since 5 days, diarrhoea and nausea. There was no fever or muscular guarding, and no signs of inflammation in the blood screening. An ultrasound and a CT-scan of
Autor:
Hanno L. Tan, Albert C. van Rossum, Frans van Hoorn, Anje M. Spijkerboer, Jacques M.T. de Bakker, Maarten Groenink, Marieke T. Blom, Arthur A.M. Wilde, R. Nils Planken, Maria E. Campian
Publikováno v:
PLoS ONE, 7(8). Public Library of Science
PLoS ONE, 7(8):e42037. Public Library of Science
PLoS ONE, Vol 7, Iss 8, p e42037 (2012)
PLoS ONE
van Hoorn, F, Campian, M E, Spijkerboer, A, Blom, M T, Planken, R N, van Rossum, A C, de Bakker, J M T, Wilde, A A M, Groenink, M & Tan, H L 2012, ' Scn5a mutations in brugada syndrome are associated with increased cardiac dimensions and reduced contractility ', PLoS ONE, vol. 7, no. 8, e42037 . https://doi.org/10.1371/journal.pone.0042037
PLoS ONE, 7(8):e42037. Public Library of Science
PLoS ONE, Vol 7, Iss 8, p e42037 (2012)
PLoS ONE
van Hoorn, F, Campian, M E, Spijkerboer, A, Blom, M T, Planken, R N, van Rossum, A C, de Bakker, J M T, Wilde, A A M, Groenink, M & Tan, H L 2012, ' Scn5a mutations in brugada syndrome are associated with increased cardiac dimensions and reduced contractility ', PLoS ONE, vol. 7, no. 8, e42037 . https://doi.org/10.1371/journal.pone.0042037
Background: The cardiac sodium channel (Nav1.5) controls cardiac excitability. Accordingly, SCN5A mutations that result in loss-of-function of Nav1.5 are associated with various inherited arrhythmia syndromes that revolve around reduced cardiac excit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5362661365d11cfac3bcb7faca70a029
https://pure.amc.nl/en/publications/scn5a-mutations-in-brugada-syndrome-are-associated-with-increased-cardiac-dimensions-and-reduced-contractility(c7492013-5b64-4099-a555-38afb080f394).html
https://pure.amc.nl/en/publications/scn5a-mutations-in-brugada-syndrome-are-associated-with-increased-cardiac-dimensions-and-reduced-contractility(c7492013-5b64-4099-a555-38afb080f394).html
Publikováno v:
European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery. 29(6)
Autor:
Rachel Wald, Elsie T Nguyen, Danna A. Spears, Janice Paproski, Sebastian Ley, Narinder Paul, Bernd J. Wintersperger, Frans van Hoorn, Felipe Soares Torres, Andrew M. Crean
Publikováno v:
Europe PubMed Central
Journal of Cardiovascular Magnetic Resonance
Journal of Cardiovascular Magnetic Resonance, Vol 14, Iss Suppl 1, p P141 (2012)
Journal of Cardiovascular Magnetic Resonance
Journal of Cardiovascular Magnetic Resonance, Vol 14, Iss Suppl 1, p P141 (2012)
Background ARVC is a rare potentially life-threatening inherited disease of the desmosome. Right ventricular wall motion abnormalities combined with right ventricular dilatation or impaired function on CMR are diagnostic criteria for this disease. Th