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Browsing by Author Schols, L.
Showing results 5 to 17 of 17
| Full Text | Issue Date | Title | Author(s) | | 2005 | L carnitine and creatine in Friedreich's ataxia. A randomized, placebo-controlled crossover trial. | Schols, L.; Zange, J.; Abele, M., et al |
| 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 |
| 2008 | REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31. | Beetz, C.; Schule, R.; Deconinck, T., 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 |
| 2010 | Responsiveness of different rating instruments in spinocerebellar ataxia patients. | Schmitz-Hubsch, T.; Fimmers, R.; Rakowicz, M., et al |
| 2008 | SCA Functional Index: a useful compound performance measure for spinocerebellar ataxia. | Schmitz-Hubsch, T.; Giunti, P.; Stephenson, D.A., 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 |
| 2008 | SPG10 is a rare cause of spastic paraplegia in European families. | Schule, R.; Kremer, B.P.; Kassubek, J., et al |
| 2009 | Spinocerebellar ataxia type 6 (SCA6): neurodegeneration goes beyond the known brain predilection sites. | Gierga, K.; Schelhaas, H.J.; Brunt, E.R., 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 | 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 5 to 17 of 17
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