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J Finsterer

Showing results (301-310 of 336) with videos related to

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Muscle & Nerve|June 17, 1998
Axonal polyneuropathy in Ehlers-Danlos syndromeW Muellbacher, J Finsterer, B Mamoli, et al.
Brain, Behavior, & Immunity - Health|December 3, 2020
Before attributing COVID_19-related ischemic stroke to hypercoagulability alternative causes should be excludedJ Finsterer, F A Scorza, C A Scorza, et al.
Kinderarztliche Praxis|June 1, 1977
[Ophthalmologic findings in congenital hypo- and athyreoses and their combination with additional disorders]V Hesse, W Krebs, W Schmäche, 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.
Pageof 34

Showing results (301-310 of 336) with videos related to

Sort By:
Pageof 34
Muscle & Nerve|June 17, 1998
Axonal polyneuropathy in Ehlers-Danlos syndromeW Muellbacher, J Finsterer, B Mamoli, et al.
Brain, Behavior, & Immunity - Health|December 3, 2020
Before attributing COVID_19-related ischemic stroke to hypercoagulability alternative causes should be excludedJ Finsterer, F A Scorza, C A Scorza, et al.
Kinderarztliche Praxis|June 1, 1977
[Ophthalmologic findings in congenital hypo- and athyreoses and their combination with additional disorders]V Hesse, W Krebs, W Schmäche, 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.
Pageof 34