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Frontiers in Cardiovascular Medicine|March 27, 2025
Predictors for long-term outcome of pulmonary valve perforation and balloon valvuloplasty in neonates with critical pulmonary valve stenosis or pulmonary valve atresia with intact ventricular septumTariq Abu-Tair, Ines Willershausen, Melanie Friedmann, et al.Journal of the American College of Cardiology|November 13, 2002
Cardiac manifestations of Anderson-Fabry disease in heterozygous femalesChristoph Kampmann, Frank Baehner, Catharina Whybra, et al.European Heart Journal|May 8, 2007
Cardiac manifestations of Anderson-Fabry disease: results from the international Fabry outcome surveyAles Linhart, Christoph Kampmann, José L Zamorano, et al.Pediatric Radiology|November 26, 2002
Biodegradation of tungsten embolisation coils used in childrenChristoph Kampmann, Rita Brzezinska, Moji Abidini, et al.The American Journal of Cardiology|February 27, 2010
PQ interval in patients with Fabry diseaseMehdi Namdar, Christoph Kampmann, Jan Steffel, et al.Orphanet Journal of Rare Diseases|March 3, 2022
Addressing the need for patient-friendly medical communications: adaptation of the 2019 recommendations for the management of MPS VI and MPS IVAIain A Bruce, Fatih S Ezgü, Christoph Kampmann, et al.Journal of Inherited Metabolic Disease|September 25, 2013
Mucopolysaccharidosis VI: cardiac involvement and the impact of enzyme replacement therapyChristoph Kampmann, Christina Lampe, Catharina Whybra-Trümpler, et al.Frontiers in Pharmacology|June 1, 2022
The Inflammation in the Cytopathology of Patients With Mucopolysaccharidoses- Immunomodulatory Drugs as an Approach to TherapyAnna-Maria Wiesinger, Brian Bigger, Roberto Giugliani, et al.Diagnostics (Basel, Switzerland)|March 14, 2026
Photon-Counting CT Enables Higher Image Quality at a Lower Radiation Dose Compared with a 256-Slice Energy-Integrating Detector CT in Pediatric Patients with Congenital Heart DiseaseAndré Lollert, Fabio Souschek, Tariq Abu-Tair, et al.Pediatric Nephrology (Berlin, Germany)|July 14, 2006
IgA nephropathy in two adolescent sisters heterozygous for Fabry diseaseCatharina Whybra, Andreas Schwarting, Jörg Kriegsmann, et al.Pageof 8