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Written informed consent was obtained for all contrast-enhanced CMR procedures. For the retrospective patient cohort, the IRB waived the requirement for individual consent given the anonymized use of pre-existing clinical data.","order":2,"name":"Ethics","group":{"name":"EthicsHeading","label":"Ethical approval"}},{"value":"Informed consent was waived by the Ethics Committee for the retrospective patient cohort. Written informed consent was obtained from all prospectively enrolled healthy control participants.T.","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Consent to participate"}},{"value":"Not applicable.","order":4,"name":"Ethics","group":{"name":"EthicsHeading","label":"Consent for publication"}},{"value":"The authors declare no competing interests.","order":5,"name":"Ethics","group":{"name":"EthicsHeading","label":"Competing interests"}}],"article-number":"21"}}