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Browsing by Author Durr, A.
Showing results 8 to 17 of 17
| Full Text | Issue Date | Title | Author(s) | | 2011 | The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study | Jacobi, H.; Bauer, P.; Giunti, P., et al |
| 2006 | Reliability and validity of the International Cooperative Ataxia Rating Scale: a study in 156 spinocerebellar ataxia patients. | Schmitz-Hubsch, T.; Montcel, S.T. du; Baliko, L., et al |
| 2006 | Scale for the assessment and rating of ataxia: development of a new clinical scale. | Schmitz-Hubsch, T.; Montcel, S.T. du; Baliko, L., et al |
| 2010 | Self-rated health status in spinocerebellar ataxia--results from a European multicenter study. | Schmitz-Hubsch, T.; Coudert, M.; Giunti, P., et al |
| 2012 | Spinocerebellar ataxia types 1, 2, 3 and 6: the clinical spectrum of ataxia and morphometric brainstem and cerebellar findings. | Jacobi, H.; Hauser, T.K.; Giunti, P., et al |
| 2008 | Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms. | Schmitz-Hubsch, T.; Coudert, M.; Bauer, P., et al |
| 2010 | Targeted next-generation sequencing of a 12.5 Mb homozygous region reveals ANO10 mutations in patients with autosomal-recessive cerebellar ataxia. | Vermeer, S.; Hoischen, A.; Meijer, R.P., et al |
| 2011 | A two-stage meta-analysis identifies several new loci for Parkinson's disease. | Plagnol, V.; Nalls, M.A.; Bras, J.M., et al |
| 2012 | Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease | Keller, M.F.; Saad, M.; Bras, J., et al |
| 2010 | Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6. | Schulz, J.B.; Borkert, J.; Wolf, S., et al |
Showing results 8 to 17 of 17
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