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Archives of Neurology|August 1, 1993
Late-onset Friedreich's ataxia. Molecular genetics, clinical neurophysiology, and magnetic resonance imagingT Klockgether, S Chamberlain, U Wüllner, et al.Neurology|January 1, 1996
Friedreich's ataxia with retained tendon reflexes: molecular genetics, clinical neurophysiology, and magnetic resonance imagingT Klockgether, C Zühlke, J B Schulz, et al.European Neurology|September 28, 1998
Acute disseminated encephalomyelitis following Pontiac feverS Spieker, D Petersen, A Rolfs, et al.Brain : a Journal of Neurology|October 1, 1996
Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3K Bürk, M Abele, M Fetter, et al.Human Neurobiology|January 1, 1984
Clinical symptoms of cerebellar dysfunction and their topodiagnostical significanceJ DichgansHandbook of Clinical Neurology|September 18, 2016
Acute unilateral loss of vestibular functionM FetterClinical Research in Cardiology : Official Journal of the German Cardiac Society|April 7, 2006
[Diabetes and cerebrovascular disease]M FetterBrain Research Bulletin|January 1, 1996
Three-dimensional orientation of the eye rotation axis during the Purkinje sensationM FetterPageof 35