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Journal of Cardiovascular Electrophysiology|April 25, 2014
Repeated radiofrequency ablation of atrial tachycardia in restrictive cardiomyopathy secondary to myofibrillar myopathyClaudia Stöllberger, Edmund Gatterer, Josef Finsterer, et al.
Acute Cardiac Care|August 8, 2014
Recurrent takotsubo syndrome in a patient with myotonic dystrophy 1Josef Finsterer, Claudia Stöllberger, Dita Demirtas, et al.
Redox Report : Communications in Free Radical Research|May 16, 2023
Relevance of oxidative stress biomarkers, hemoglobin A1c, troponin-I, and angiotensin-converting enzyme metabolism to blood pressure in acute myocardial infarction: a case-control studySounira Mehri, Raja Chaaba, Josef Finsterer, et al.
ISRN Cardiology|July 20, 2012
Novel m.15434C>A (p.230L>I) Mitochondrial Cytb Gene Missense Mutation Associated with Dilated CardiomyopathySinda Zarrouk Mahjoub, Sounira Mehri, Fatma Ourda, et al.
Parkinsonism & Related Disorders|September 8, 2018
Sudden death in Parkinson's disease: Unjustifiably forgottenMariana B Nejm, Monica L Andersen, Sergio Tufik, et al.
Intractable & Rare Diseases Research|June 5, 2018
Muscular and cardiac manifestations in a Duchenne-carrier harboring a dystrophin deletion of exons 12-29Josef Finsterer, Claudia Stöllberger, Birgit Freudenthaler, et al.
Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|April 15, 2014
Familial Himalayan p wave and left ventricular hypertrabeculation/noncompactionClaudia Stöllberger, Marion Avanzini, Peter Siostrzonek, et al.
Acta Neurologica Scandinavica|October 9, 2018
Hereditary transthyretin-related amyloidosisJosef Finsterer, Stephan Iglseder, Julia Wanschitz, et al.
Neuromuscular Disorders : NMD|June 24, 2014
Distal myosin heavy chain-7 myopathy due to the novel transition c.5566G>A (p.E1856K) with high interfamilial cardiac variability and putative anticipationJosef Finsterer, Oliver Brandau, Claudia Stöllberger, et al.
Clinical Case Reports|February 10, 2022
MELAS with multiple stroke-like episodes due to the variant m.13513G>A in MT-ND5Ritwik Ghosh, Souvik Dubey, Subhas Bhuin, et al.
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