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Page 1
alpha-Synuclein and Parkinson disease susceptibility.
Winkler S, Hagenah J, Lincoln S, Heckman M, Haugarvoll K, Lohmann-Hedrich K, Kostic V, Farrer M, Klein C. Winkler S, et al. Among authors: lohmann hedrich k. Neurology. 2007 Oct 30;69(18):1745-50. doi: 10.1212/01.wnl.0000275524.15125.f4. Epub 2007 Sep 13. Neurology. 2007. PMID: 17872362
Impact of recent genetic findings in Parkinson's disease.
Klein C, Lohmann-Hedrich K. Klein C, et al. Among authors: lohmann hedrich k. Curr Opin Neurol. 2007 Aug;20(4):453-64. doi: 10.1097/WCO.0b013e3281e6692b. Curr Opin Neurol. 2007. PMID: 17620882 Review.
Biological effects of the PINK1 c.1366C>T mutation: implications in Parkinson disease pathogenesis.
Grünewald A, Breedveld GJ, Lohmann-Hedrich K, Rohé CF, König IR, Hagenah J, Vanacore N, Meco G, Antonini A, Goldwurm S, Lesage S, Dürr A, Binkofski F, Siebner H, Münchau A, Brice A, Oostra BA, Klein C, Bonifati V. Grünewald A, et al. Among authors: lohmann hedrich k. Neurogenetics. 2007 Apr;8(2):103-9. doi: 10.1007/s10048-006-0072-y. Epub 2007 Jan 12. Neurogenetics. 2007. PMID: 17219214
Myoclonus-dystonia: significance of large SGCE deletions.
Grünewald A, Djarmati A, Lohmann-Hedrich K, Farrell K, Zeller JA, Allert N, Papengut F, Petersen B, Fung V, Sue CM, O'Sullivan D, Mahant N, Kupsch A, Chuang RS, Wiegers K, Pawlack H, Hagenah J, Ozelius LJ, Stephani U, Schuit R, Lang AE, Volkmann J, Münchau A, Klein C. Grünewald A, et al. Among authors: lohmann hedrich k. Hum Mutat. 2008 Feb;29(2):331-2. doi: 10.1002/humu.9521. Hum Mutat. 2008. PMID: 18205193
Myoclonus-dystonia due to maternal uniparental disomy.
Guettard E, Portnoi MF, Lohmann-Hedrich K, Keren B, Rossignol S, Winkler S, El Kamel I, Leu S, Apartis E, Vidailhet M, Klein C, Roze E. Guettard E, et al. Among authors: lohmann hedrich k. Arch Neurol. 2008 Oct;65(10):1380-5. doi: 10.1001/archneur.65.10.1380. Arch Neurol. 2008. PMID: 18852357