Genetics in Parkinson’s disease
Has parts
Paper I: European Journal of Neurology 10(2), Kurz, M.; Alves, G.; Aarsland, D.; Larsen, J. P., Familial Parkinson's disease: a community-based study, pp. 159-63. Copyright 2003 Blackwell Publishing. Fulltext not available due to publisher restrictions. Published version available at: http://dx.doi.org/10.1046/j.1468-1331.2003.00532.xPaper II: Acta Neurology Scandinavia 113(1), Schlitter, A. M.; Kurz, M.; Larsen, J. P.; Woitalla, D.; Mueller, T.; Epplen, J. T.; Dekomien, G., Parkin gene variations in late-onset Parkinson's disease: comparison between Norwegian and German cohorts, pp. 9-13. Copyright 2006 Blackwell Publishing. Fulltext not available due to publisher restrictions. Published version available at: http://dx.doi.org/10.1111/j.1600-0404.2005.00532.x
Paper III: Journal of Negative Results in Biomedicine 4(10), Schlitter, A. M.: Kurz, M.; Larsen, J. P.; Woitalla, D.; Mueller, T.; Epplen, J. T.; Dekomien. G., Exclusion of PINK1 as candidate gene for the late-onset form of Parkinson's disease in 2 European populations. Copyright © 2005 Schlitter et al; licensee BioMed Central Ltd. Published version available at: http://dx.doi.org/10.1186/1477-5751-4-10
Paper IV: Dementia and Geriatric Cognitive Disorders 22(4), Kurz, M. W.; Schlitter, A. M.; Larsen, J. P.; Ballard, C.; Aarsland, D., Familial occurrence of dementia and parkinsonism. A systematic review, pp. 88-95. Copyright 2006 S. Karger AG. Fulltext not available due to publisher restrictions. Published version available at: http://dx.doi.org/10.1159/000095159