Milan Prsa (Milan Prša)

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 6

Top Topics

Congenital Heart Disease

Magnetic Resonance

Coronary Artery

Top Venues

Magnetic resonance in medicine

Cardiology in the young

Genetics in medicine : official journal of the American College of Medical Genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Ludovica Romanin, Bastien Milani, Christopher W Roy, Jérôme Yerly, Aurélien Bustin, Salim Si-Mohamed, Milan Prsa, Tobias Rutz, Estelle Tenisch, Juerg Schwitter, Matthias Stuber, Davide Piccini
Similarity-driven motion-resolved reconstruction for ferumoxytol-enhanced whole-heart MRI in congenital heart disease. PloS one 19 (6) (2024)
Ludovica Romanin, Bastien Milani, Christopher W Roy, Jérôme Yerly, Aurélien Bustin, Salim Si-Mohamed, Milan Prsa, Tobias Rutz, Estelle Tenisch, Juerg Schwitter, Matthias Stuber, Davide Piccini
Similarity-driven motion-resolved reconstruction for ferumoxytol-enhanced whole-heart MRI in congenital heart disease. PloS one 19 (6) (2024)
Mariana B L Falcão, Giulia M C Rossi, Tobias Rutz, Milan Prsa, Estelle Tenisch, Liliana E Ma, Elizabeth K Weiss, Justin J Baraboo, Jérôme Yerly, Michael Markl, Matthias Stuber, Christopher W Roy
Focused navigation for respiratory-motion-corrected free-running radial 4D flow MRI. Magnetic resonance in medicine (2023)
Mariana B L Falcão, Lorenzo Di Sopra, Liliana E Ma, Mario Bacher, Jérôme Yerly, Peter Speier, Tobias Rutz, Milan Prsa, Michael Markl, Matthias Stuber, Christopher W Roy
Pilot tone navigation for respiratory and cardiac motion-resolved free-running 5D flow MRI. Magnetic resonance in medicine 87 (2) (2021)
Ibrahima S Barry, Stefano Di Bernardo, Milan Prsa
Coronary artery to pulmonary artery collateral as the principal source of pulmonary blood supply in pulmonary atresia and ventricular septal defect with absent left pulmonary artery. Cardiology in the young 30 (11) (2020)
Josephina A N Meester, Geert Vandeweyer, Isabel Pintelon, Martin M Y Lammens, Lana Van Hoorick, Simon De Belder, Kathryn Waitzman, Luciana Young, Larry W Markham, Julie Vogt, Julie Richer, Luc M Beauchesne, Sheila Unger, Andrea Superti-Furga, Milan Prsa, Rami Dhillon, Edwin Reyniers, Harry C Dietz, Wim Wuyts, Geert Mortier, Aline Verstraeten, Lut Van Laer, Bart L Loeys
Loss-of-function mutations in the X-linked biglycan gene cause a severe syndromic form of thoracic aortic aneurysms and dissections. Genetics in medicine : official journal of the American College of Medical Genetics 19 (4) (2016)