Showing results (181-190 of 208) with videos related to
Sort By:
Pageof 21
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.Journal of Toxicology. Clinical Toxicology|August 26, 1998
Malnutrition-induced hypokalemic myopathy in chronic alcoholismJ Finsterer, B Hess, C Jarius, et al.Acta Neurologica Scandinavica|March 16, 2017
Causally treatable, hereditary neuropathies in Fabry's disease, transthyretin-related familial amyloidosis, and Pompe's diseaseJ Finsterer, J Wanschitz, S Quasthoff, et al.Cephalalgia : an International Journal of Headache|November 25, 1998
Headache as the initial manifestation of acute aortic dissection type AC Stöllberger, J Finsterer, C Fousek, et al.Clinical Genetics|April 29, 1998
Genotype-phenotype correlation in myotonic dystrophyE B Gharehbaghi-Schnell, J Finsterer, I Korschineck, et al.Acta Clinica Belgica|July 4, 2015
Myotonic dystrophy 2 manifesting with non-alcoholic and non-hepatitic liver cirrhosisJ Finsterer, A Karpatova, H Rauschka, et al.Pageof 21