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Brain Research. Molecular Brain Research|December 14, 2002
14-3-3 protein is a component of Lewy bodies in Parkinson's disease-mutation analysis and association studies of 14-3-3 etaAndreas Ubl, Daniela Berg, Carsten Holzmann, et al.
Brain Research|September 17, 2002
Neurofilament L gene is not a genetic factor of sporadic and familial Parkinson's diseaseNils Rahner, Carsten Holzmann, Rejko Krüger, et al.
Journal of Neurology|May 23, 2003
Therapeutic strategies for Parkinson's disease based on data derived from genetic researchOlaf Riess, Daniela Berg, Rejko Krüger, et al.
Neurotoxicity Research|February 9, 2006
Disturbance of iron metabolism in Parkinson's disease -- ultrasonography as a biomarkerDaniela Berg, Helmine Hochstrasser, Katherine J Schweitzer, et al.
Journal of Neurochemistry|July 22, 2005
Regional and subtype selective changes of neurotransmitter receptor density in a rat transgenic for the Huntington's disease mutationAndreas Bauer, Karl Zilles, Andreas Matusch, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|March 4, 2009
Genetic analysis of coding SNPs in blood-brain barrier transporter MDR1 in European Parkinson's disease patientsClaudia Funke, Anne S Soehn, Juergen Tomiuk, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|May 29, 2009
Genetic analysis of heme oxygenase-1 (HO-1) in German Parkinson's disease patientsClaudia Funke, Juergen Tomiuk, Olaf Riess, et al.
Proteomics. Clinical Applications|December 8, 2010
Age-dependent gene expression profile and protein expression in a transgenic rat model of Huntington's diseaseHuu Phuc Nguyen, Silke Metzger, Carsten Holzmann, et al.
Neurobiology of Aging|February 19, 2008
Further delineation of the association signal on chromosome 5 from the first whole genome association study in Parkinson's diseaseManu Sharma, Peter Lichtner, Rejko Kruger, et al.
Human Molecular Genetics|August 12, 2009
Reversibility of symptoms in a conditional mouse model of spinocerebellar ataxia type 3Jana Boy, Thorsten Schmidt, Hartwig Wolburg, et al.
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