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Molecular Genetics & Genomic Medicine|February 25, 2022
Gene variants of unknown significance in Fabry disease: Clinical characteristics of c.376A>G (p.Ser126Gly)Kolja Lau, Nurcan Üçeyler, Tereza Cairns, et al.
BMJ Open|April 10, 2016
Organ manifestations and long-term outcome of Fabry disease in patients with the GLA haplotype D313YDaniel Oder, Nurcan Üçeyler, Dan Liu, et al.
World Journal of Cardiology|July 2, 2015
Long term evolution of magnetic resonance imaging characteristics in a case of atypical left lateral wall hypertrophic cardiomyopathyTobias Gassenmaier, Bernhard Petritsch, Andreas S Kunz, et al.
ESC Heart Failure|May 17, 2019
Impella CP use in patients with non-ischaemic cardiogenic shockOctavian Maniuc, Tim Salinger, Fabian Anders, et al.
NMR in Biomedicine|June 26, 2024
Quantification of the rotating frame relaxation time T2ρ: Comparison of balanced spin-lock and continuous-wave Malcolm-Levitt preparationsMaximilian Gram, Martin Christa, Fabian Tobias Gutjahr, et al.
Journal of Inherited Metabolic Disease|April 15, 2024
Genetic variants of unknown significance in alpha-galactosidase A: Cellular delineation from Fabry diseaseAlexandra Klein, Katharina Klug, Maximilian Breyer, et al.
Journal of Medical Genetics|September 2, 2025
Long-term efficacy of migalastat in females with Fabry diseaseStaci Kallish, Antonia Camporeale, Robert J Hopkin, et al.
Magma (New York, N.Y.)|September 7, 2021
Fast myocardial T1ρ mapping in mice using k-space weighted image contrast and a Bloch simulation-optimized radial sampling patternMaximilian Gram, Daniel Gensler, Patrick Winter, et al.
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