Programmdetails

Mitochondrial distribution in tachycardiomyopathy

Comprehensive quantitative description of nuclear and cellular morphology and orientation in tachycardiomyopathy

Morbus Fabry als Differentialdiagnose der Hypertrophen Kardiomyopathie: Eine prospektive Diagnostikstudie zur nachträglichen genetischen Testung anhand vorliegender elektronischer Patientendaten

Correlation of Cardiomyopathy Severity Measured by Echo and Quality of Life in Patients with Fabry Disease

Troponinerhöhung bei Patienten mit Muskeldystrophien - Bewertung mittels kardiovaskulärer Magnetresonanztomographie

Outcome of subtotal pericardiectomy for constrictive pericarditis - Lessons from a single centre experience

Novel histopathological risk factors for patients with Tachycardiomyopathy

Mid- to long-term biovariability of hs-cTnT within 6-12 months in Muscular Dystrophic Cardiomyopathy: An Observational Study on 35 patients.