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Neurology|December 17, 1998
Sleep disturbance in spinocerebellar ataxias: is the SCA3 mutation a cause of restless legs syndrome?L Schöls, J Haan, O Riess, et al.Human Genetics|February 1, 1997
Transmission distortion of the mutant alleles in spinocerebellar ataxiaO Riess, J T Epplen, G Amoiridis, et al.Der Nervenarzt|December 1, 1996
[Drug-induced rhabdomyolysis and lesions of peripheral nerves. Sequelae of local ischemia within the scope of circulatory collapse?]G Amoiridis, L Schöls, D Pöhlau, et al.Brain : a Journal of Neurology|February 4, 1998
Friedreich's ataxia. Revision of the phenotype according to molecular geneticsL Schöls, G Amoiridis, H Przuntek, et al.Zeitschrift Fur Gastroenterologie|August 1, 1992
[Gallbladder motility in diabetic patients with and without cardiovascular neuropathy]B Wedmann, C Dröge, G Amoiridis, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1996
Relations between genotype and phenotype in German patients with the Machado-Joseph disease mutationL Schöls, G Amoiridis, J T Epplen, et al.Fortschritte Der Neurologie-Psychiatrie|February 1, 1997
[Genetic diagnosis, classification and clinical hereditary ataxia disease entities]L Schöls, O Riess, G Amoiridis, et al.Journal of Neurology, Neurosurgery, and Psychiatry|January 22, 1998
Spinocerebellar ataxia type 6: genotype and phenotype in German kindredsL Schöls, R Krüger, G Amoiridis, et al.Annals of Neurology|December 24, 1997
Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?L Schöls, G Amoiridis, T Büttner, et al.Current Eye Research|May 29, 2012
Correlation of diabetic retinopathy and corneal neuropathy using confocal microscopyE Nitoda, P Kallinikos, A Pallikaris, et al.Pageof 3