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You searched for: Author/Creator Tiesmeier, Jens

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1. A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy. (April 2020)

2. Cardiomyopathy‐associated mutations in the RS domain affect nuclear localization of RBM20. Issue 11 (9th September 2020)

3. Mechanical circulatory support does not reduce advanced myocardial fibrosis in patients with end‐stage heart failure. (12th November 2020)

4. Molecular autopsy and family screening in a young case of sudden cardiac death reveals an unusually severe case of FHL1 related hypertrophic cardiomyopathy. Issue 8 (10th July 2019)

5. The emergency medical service has a crucial role to unravel the genetics of sudden cardiac arrest in young, out of hospital resuscitated patients: Interim data from the MAP-IT study. (November 2021)