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Browsing by Author Schols, L.

Full Text	Issue Date	Title	Author(s)
	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
	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