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Browsing by Author Brice, A.

Full Text	Issue Date	Title	Author(s)
	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., et al
	2009	Cerebellar Ataxia and Elevated Cerebrospinal Free Sialic Acid	Mochel, F.; Sedel, F.; Vanderver, A., et al
	2009	Cerebellar ataxia with elevated cerebrospinal free sialic acid (CAFSA).	Mochel, F.; Sedel, F.; Vanderver, A., et al
	2011	Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies	Nalls, M.A.; Plagnol, V.; Hernandez, D.G., et al
	2006	Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations.	Azzedine, H.; Ravise, N.; Verny, C., 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