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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.
Annals of Burns and Fire Disasters|July 8, 2024
[DISTRIBUTION OF CARBAPENEMASES IN TUNISIAN BURN PATIENTS]A Mokline, S Zarrouk, I Jemi, et al.
Thrombosis Research|March 10, 2000
Multivariate analysis-based prediction rule for pulmonary embolismC Stöllberger, J Finsterer, W Lutz, et al.
Journal of the Neurological Sciences|April 15, 1997
Light chain myeloma with oro-pharyngeal amyloidosis presenting as bulbar paralysisJ Finsterer, C Wogritsch, P Pokieser, et al.
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