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Zschiedrich K, König IR, Brüggemann N, Kock N, Kasten M, Leenders KL, et al. MDR1 variants and risk of Parkinson disease. Association with pesticide exposure? J Neurol. 2009;256(1):115-20.
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Biskup S, Gerlach M, Kupsch A, Reichmann H, Riederer P, Vieregge P, et al. Genes associated with Parkinson syndrome. J Neurol. 2008;255 Suppl 5:8-17.
Djarmati A, Guzvić M, Grünewald A, Lang AE, Pramstaller PP, Simon DK, et al. Rapid and reliable detection of exon rearrangements in various movement disorders genes by multiplex ligation-dependent probe amplification. Mov Disord. 2007;22(12):1708-14.
Winkler S, König IR, Lohmann-Hedrich K, Vieregge P, Kostic V, Klein C. Role of ethnicity on the association of MAPT H1 haplotypes and subhaplotypes in Parkinson's disease. Eur J Hum Genet. 2007;15(11):1163-8.
Hedrich K, Eskelson C, Wilmot B, Marder K, Harris J, Garrels J, et al. Distribution, type, and origin of Parkin mutations: review and case studies. Mov Disord. 2004;19(10):1146-57.
Zimprich A, Biskup S, Leitner P, Lichtner P, Farrer M, Lincoln S, et al. Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology. Neuron. 2004;44(4):601-7.
Hedrich K, Schäfer N, Hering R, Hagenah J, Lanthaler AJ, Schwinger E, et al. The R98Q variation in DJ-1 represents a rare polymorphism. Ann Neurol. 2004;55(1):145; author reply 145-6.
DeStefano AL, Lew MF, Golbe LI, Mark MH, Lazzarini AM, Guttman M, et al. PARK3 influences age at onset in Parkinson disease: a genome scan in the GenePD study. Am J Hum Genet. 2002;70(5):1089-95.