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European Neurology|July 15, 2000
Complex mitochondriopathy associated with 4 mtDNA transitionsJ Finsterer, R Bittner, M Bodingbauer, et al.Deutsche Medizinische Wochenschrift (1946)|July 14, 2007
[Merkel cell carcinoma--clinically often misjudged]H Weisser, W Hartschuh, A Greiner, 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.Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]|June 1, 1995
[Bicentric stereotaxic convergent-beam irradiation]M Bischof, J Major, G Christ, 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 Oral Implants Research|August 23, 2024
Survival and complication rates of tooth- and implant-supported restorations after an observation period up to 36 yearsFrank M Bischof, Ayse A Mathey, Alexandra Stähli, et al.The Journal of Allergy and Clinical Immunology|September 1, 1987
A double-blind study comparing monomethoxy polyethylene glycol-modified honeybee venom and unmodified honeybee venom for immunotherapy. I. Clinical resultsU Müller, A R Rabson, M Bischof, et al.Clinical Genetics|April 29, 1998
Genotype-phenotype correlation in myotonic dystrophyE B Gharehbaghi-Schnell, J Finsterer, I Korschineck, et al.Pageof 28