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Browsing by Author Schols, L.

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.; Labrum, R.; Sweeney, M.G., et al
	2011	Depression comorbidity in spinocerebellar ataxia	Schmitz-Hubsch, T.; Coudert, M.; Tezenas du Montcel, S.; Giunti, P.; Labrum, R., 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.; Schmitz-Hubsch, T.; Rakowicz, M., et al
	2010	Falls in spinocerebellar ataxias: Results of the EuroSCA Fall Study.	Fonteyn, E.M.; Schmitz-Hubsch, T.; Verstappen, C.C.P.; Baliko, L.; Bloem, B.R., et al
	2010	Responsiveness of different rating instruments in spinocerebellar ataxia patients.	Schmitz-Hubsch, T.; Fimmers, R.; Rakowicz, M.; Rola, R.; Zdzienicka, E., et al
	2010	Self-rated health status in spinocerebellar ataxia--results from a European multicenter study.	Schmitz-Hubsch, T.; Coudert, M.; Giunti, P.; Globas, C.; Baliko, L., et al
	2009	Spinocerebellar ataxia type 6 (SCA6): neurodegeneration goes beyond the known brain predilection sites.	Gierga, K.; Schelhaas, H.J.; Brunt, E.R.; Seidel, K.; Scherzed, W., et al
	2009	Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24.	Schule, R.; Bonin, M.; Durr, A.; Forlani, S.; Sperfeld, A.D., et al
	2008	Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms.	Schmitz-Hubsch, T.; Coudert, M.; Bauer, P.; Giunti, P.; Globas, C., et al
	2008	REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31.	Beetz, C.; Schule, R.; Deconinck, T.; Tran-Viet, K.N.; Zhu, H., et al
	2008	Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6.	Globas, C.; Montcel, S.T. du; Baliko, L.; Boesch, S.; Depondt, C., et al
	2008	SPG10 is a rare cause of spastic paraplegia in European families.	Schule, R.; Kremer, B.P.; Kassubek, J.; Auer-Grumbach, M.; Kostic, V., et al
	2008	SCA Functional Index: a useful compound performance measure for spinocerebellar ataxia.	Schmitz-Hubsch, T.; Giunti, P.; Stephenson, D.A.; Globas, C.; Baliko, L., 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.; Boesch, S.; Bonato, S., 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.; Berciano, J.; Boesch, S., et al
	2005	L carnitine and creatine in Friedreich's ataxia. A randomized, placebo-controlled crossover trial.	Schols, L.; Zange, J.; Abele, M.; Schillings, M.L.; Skipka, G., et al