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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.Artificial Organs|March 7, 2002
Patient safety technology for microadsorbent systems in extracorporeal blood purificationD Falkenhagen, W Strobl, J Hartmann, et al.The Journal of Biological Chemistry|January 15, 1989
Effect of sucrose diet on apolipoprotein biosynthesis in rat liver. Increase in apolipoprotein E gene transcriptionW Strobl, N L Gorder, G A Fienup, et al.Journal of Investigative Medicine : the Official Publication of the American Federation for Clinical Research|October 8, 1999
Up-regulation of LDL-receptor expression by LDL-immunoapheresis in patients with familial hypercholesterolemiaJ Streicher, P Valent, H Schmidt, 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 24