Your search returned 7 results.

Results
	1.	Trinucleotide expansion within the MJD1 gene presents clinically as spinocerebellar ataxia and occurs most frequently in German SCA patients. [electronic resource] by Schöls, L Vieira-Saecker, A M Schöls, S Przuntek, H Epplen, J T Riess, O Producer: 19951005 In: Human molecular genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Machado-Joseph disease mutations as the genetic basis of most spinocerebellar ataxias in Germany. [electronic resource] by Schöls, L Amoiridis, G Langkafel, M Büttner, T Przuntek, H Riess, O Vieira-Saecker, A M Epplen, J T Producer: 19951103 In: Journal of neurology, neurosurgery, and psychiatry vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel gene. [electronic resource] by Riess, O Schöls, L Bottger, H Nolte, D Vieira-Saecker, A M Schimming, C Kreuz, F Macek, M Krebsová, A Klockgether, T Zühlke, C Laccone, F A Producer: 19971030 In: Human molecular genetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds. [electronic resource] by Schöls, L Gispert, S Vorgerd, M Menezes Vieira-Saecker, A M Blanke, P Auburger, G Amoiridis, G Meves, S Epplen, J T Przuntek, H Pulst, S M Riess, O Producer: 19971023 In: Archives of neurology vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotype. [electronic resource] by Krüger, R Vieira-Saecker, A M Kuhn, W Berg, D Müller, T Kühnl, N Fuchs, G A Storch, A Hungs, M Woitalla, D Przuntek, H Epplen, J T Schöls, L Riess, O Producer: 19990525 In: Annals of neurology vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	DNA analysis of Huntington's disease: five years of experience in Germany, Austria, and Switzerland. [electronic resource] by Laccone, F Engel, U Holinski-Feder, E Weigell-Weber, M Marczinek, K Nolte, D Morris-Rosendahl, D J Zühlke, C Fuchs, K Weirich-Schwaiger, H Schlüter, G von Beust, G Vieira-Saecker, A M Weber, B H Riess, O Producer: 19991029 In: Neurology vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	SCA2 trinucleotide expansion in German SCA patients. [electronic resource] by Riess, O Laccone, F A Gispert, S Schöls, L Zühlke, C Vieira-Saecker, A M Herlt, S Wessel, K Epplen, J T Weber, B H Kreuz, F Chahrokh-Zadeh, S Meindl, A Lunkes, A Aguiar, J Macek, M Krebsová, A Macek, M Bürk, K Tinschert, S Schreyer, I Pulst, S M Auburger, G Producer: 20000411 In: Neurogenetics vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)