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The American Journal of Pathology|February 11, 2017
Cardiomyocyte Hypertrophy in Arrhythmogenic CardiomyopathyMustafa Gerçek, Muhammed Gerçek, Sebastian Kant, et al.
Cardiovascular Research|June 14, 2006
Composite polymorphisms in the ryanodine receptor 2 gene associated with arrhythmogenic right ventricular cardiomyopathyHendrik Milting, Nina Lukas, Bärbel Klauke, et al.
Aging Cell|June 26, 2023
Sex and age differences in AMPK phosphorylation, mitochondrial homeostasis, and inflammation in hearts from inflammatory cardiomyopathy patientsMaria Luisa Barcena, Greta Tonini, Natalie Haritonow, et al.
Aging|December 11, 2020
Dilated cardiomyopathy impairs mitochondrial biogenesis and promotes inflammation in an age- and sex-dependent mannerMaria Luisa Barcena, Sofya Pozdniakova, Natalie Haritonow, et al.
Frontiers in Immunology|March 11, 2021
Case Report: Early Transplant Rejection of a Methanol-Intoxicated Donor Heart in a Young Female Patient. A Diagnostic Approach With CMR, Cardiac Biopsy, and Genetic Risk AssessmentLukas Stoiber, Felix Schoenrath, Christoph Knosalla, et al.
Genes|November 14, 2019
Restrictive Cardiomyopathy is Caused by a Novel Homozygous Desmin (<i>DES</i>) Mutation p.Y122H Leading to a Severe Filament Assembly DefectAndreas Brodehl, Seyed Ahmad Pour Hakimi, Caroline Stanasiuk, et al.
Interactive Cardiovascular and Thoracic Surgery|September 16, 2015
Tricuspid valve repair in patients with left-ventricular assist device implants and tricuspid valve regurgitation: propensity score-adjusted analysis of clinical outcomeCenk Oezpeker, Armin Zittermann, Lech Paluszkiewicz, et al.
Nature Communications|October 20, 2025
Apolipoprotein A-IV fibrils: structural diagnosis of mixed cardiac amyloidosisShintaro Aibara, Astrid Kassner, Edmond Wong, et al.
International Journal of Molecular Sciences|June 24, 2022
Compound Heterozygous <i>FKTN</i> Variants in a Patient with Dilated Cardiomyopathy Led to an Aberrant α-Dystroglycan PatternAnna Gaertner, Lidia Burr, Baerbel Klauke, et al.
Molecular Genetics & Genomic Medicine|December 24, 2017
A novel desmin (DES) indel mutation causes severe atypical cardiomyopathy in combination with atrioventricular block and skeletal myopathyIlona Schirmer, Mareike Dieding, Bärbel Klauke, et al.
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