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Browsing by Author Durr, A.

Full Text	Issue Date	Title	Author(s)
	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.; Globas, C.; Bauer, P., et al
	2012	Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease	Keller, M.F.; Saad, M.; Bras, J.; Bettella, F.; Nicolaou, N., et al
	2011	A two-stage meta-analysis identifies several new loci for Parkinson's disease.	Plagnol, V.; Nalls, M.A.; Bras, J.M.; Hernandez, D.; Sharma, 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.; 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	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
	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	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	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.; Gilissen, C.F.H.A.; Neveling, K., 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
	2009	Cerebellar Ataxia and Elevated Cerebrospinal Free Sialic Acid	Mochel, F.; Sedel, F.; Vanderver, A.; Engelke, U.F.H.; Yang, B.Z., et al
	2009	Cerebellar ataxia with elevated cerebrospinal free sialic acid (CAFSA).	Mochel, F.; Sedel, F.; Vanderver, A.; Engelke, U.F.H.; Barritault, J., 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	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
	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	Age at onset variance analysis in spinocerebellar ataxias : a study in a Dutch-French cohort	Warrenburg, B.P.C. van de; Hendriks, H.; Durr, A.; Zuijlen, M.C.A. van; Stevanin, G., et al