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Cardiology|January 20, 1999
Progression of cardiac involvement in patients with myotonic dystrophy, Becker's muscular dystrophy and mitochondrial myopathy during a 2-year follow-upC Stöllberger, J Finsterer, H Keller, et al.Irish Journal of Medical Science|December 17, 2010
Coronary angiography in noncompaction with and without neuromuscular disordersC Stöllberger, J Finsterer, G Blazek, et al.Acta Neurologica Scandinavica|February 27, 2016
Secondary myopathy due to systemic diseasesJ Finsterer, W N Löscher, J Wanschitz, et al.Clinical Genetics|May 22, 2001
Relation of cardiac abnormalities and CTG-repeat size in myotonic dystrophyJ Finsterer, E Gharehbaghi-Schnell, C Stöllberger, et al.Journal of Clinical Pathology|May 1, 1996
Anti-GM1 antibodies in polyneuropathies of unknown originJ Finsterer, W Muellbacher, W M Halbmayer, et al.The Medical Journal of Malaysia|July 30, 2020
Periodic weakness of the diaphragm as the sole manifestation of bulbar onset myastheniaJ Finsterer, C A Scorza, F A Scorza, et al.Current Neurology and Neuroscience Reports|March 24, 2018
Takotsubo Syndrome: Clinical Features, Pathogenesis, Treatment, and Relationship with Cerebrovascular DiseasesM Ranieri, J Finsterer, G Bedini, et al.Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|October 11, 2001
Intramyocardial hematoma mimicking abnormal left ventricular trabeculationC Stöllberger, J Finsterer, F R Waldenberger, et al.European Neurology|July 15, 2000
Complex mitochondriopathy associated with 4 mtDNA transitionsJ Finsterer, R Bittner, M Bodingbauer, et al.Wiener Klinische Wochenschrift|March 21, 1998
Myotonic dystrophy: molecular genetics and diagnosisE Gharehbaghi-Schnell, J Finsterer, I Korschineck, et al.Pageof 20