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Brain : a Journal of Neurology|October 8, 1998
Autosomal dominant cerebellar ataxia type I. MRI-based volumetry of posterior fossa structures and basal ganglia in spinocerebellar ataxia types 1, 2 and 3T Klockgether, M Skalej, D Wedekind, et al.Neurology|March 17, 1999
Spinocerebellar ataxia type 6: evidence for a strong founder effect among German familiesM Dichgans, L Schöls, J Herzog, et al.Neuropediatrics|December 7, 2007
Folate receptor autoantibodies and spinal fluid 5-methyltetrahydrofolate deficiency in Rett syndromeV T Ramaekers, J M Sequeira, R Artuch, et al.Journal of Molecular Medicine (Berlin, Germany)|March 28, 2001
The GAA repeat expansion in intron 1 of the frataxin gene is related to the severity of cardiac manifestation in patients with Friedreich's ataxiaN Bit-Avragim, A Perrot, L Schöls, et al.Brain : a Journal of Neurology|May 13, 1998
The natural history of degenerative ataxia: a retrospective study in 466 patientsT Klockgether, R Lüdtke, B Kramer, et al.Neurology|September 17, 1999
DNA analysis of Huntington's disease: five years of experience in Germany, Austria, and SwitzerlandF Laccone, U Engel, E Holinski-Feder, et al.Journal of Medical Genetics|September 27, 2005
Gross rearrangements of the MECP2 gene are found in both classical and atypical Rett syndrome patientsH L Archer, S D Whatley, J C Evans, et al.Pageof 4