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Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions|December 1, 2016
Multicenter midterm follow-up results using the gore septal occluder for atrial septal defect closure in pediatric patientsJochen Grohmann, Christian Wildberg, Peter Zartner, et al.
Plos One|September 10, 2016
Heart and Cardiovascular Involvement in Patients with Mucopolysaccharidosis Type IVA (Morquio-A Syndrome)Christoph Kampmann, Tariq Abu-Tair, Seyfullah Gökce, et al.
Journal of Inherited Metabolic Disease|November 21, 2024
Development of a novel tool for individual treatment trials in mucopolysaccharidosisAnna-Maria Wiesinger, Brian Bigger, Roberto Giugliani, et al.
Molecular Genetics and Metabolism|May 25, 2011
Expanding the clinical spectrum of late-onset Pompe disease: dilated arteriopathy involving the thoracic aorta, a novel vascular phenotype uncoveredAreeg H El-Gharbawy, Gifty Bhat, Jaime E Murillo, et al.
Pharmaceutics|May 27, 2023
An Innovative Tool for Evidence-Based, Personalized Treatment Trials in MucopolysaccharidosisAnna-Maria Wiesinger, Brian Bigger, Roberto Giugliani, et al.
Pacing and Clinical Electrophysiology : PACE|January 5, 2007
ICD Implantation in infants and small children: the extracardiac techniqueThomas Kriebel, Wolfgang Ruschewski, Maria Gonzalez y Gonzalez, et al.
European Radiology|September 13, 2017
Differences in myocardial strain between pectus excavatum patients and healthy subjects assessed by cardiac MRI: a pilot studyAndré Lollert, Tilman Emrich, Jakob Eichstädt, et al.
International Journal of Cardiology|June 24, 2008
Onset and progression of the Anderson-Fabry disease related cardiomyopathyChristoph Kampmann, Ales Linhart, Frank Baehner, et al.
Molecular Genetics and Metabolism Reports|March 4, 2016
Long-term effectiveness of agalsidase alfa enzyme replacement in Fabry disease: A Fabry Outcome Survey analysisMichael Beck, Derralynn Hughes, Christoph Kampmann, et al.
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