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Browsing by Author Brice, A.

Full Text	Issue Date	Title	Author(s)
	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	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.; Sharma, M.; Sheerin, U.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	Cerebellar ataxia with elevated cerebrospinal free sialic acid (CAFSA).	Mochel, F.; Sedel, F.; Vanderver, A.; Engelke, U.F.H.; Barritault, J., 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
	2006	Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations.	Azzedine, H.; Ravise, N.; Verny, C.; Gabreëls-Festen, A.A.W.M.; Lammens, M.M.Y., 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