Riess O - Search Results

1

Further delineation of the association signal on chromosome 5 from the first whole genome association study in Parkinson's disease.

Sharma M, Lichtner P, Kruger R, Berg D, Schulte C, Illig T, Riess O, Gasser T. Sharma M, et al. Among authors: riess o. Neurobiol Aging. 2009 Oct;30(10):1706-9. doi: 10.1016/j.neurobiolaging.2007.12.016. Epub 2008 Feb 15. Neurobiol Aging. 2009. PMID: 18280617

2

Neurofilament L gene is not a genetic factor of sporadic and familial Parkinson's disease.

Rahner N, Holzmann C, Krüger R, Schöls L, Berger K, Riess O. Rahner N, et al. Among authors: riess o. Brain Res. 2002 Sep 27;951(1):82-6. doi: 10.1016/s0006-8993(02)03138-4. Brain Res. 2002. PMID: 12231460

3

Haploinsufficiency at the alpha-synuclein gene underlies phenotypic severity in familial Parkinson's disease.

Kobayashi H, Krüger R, Markopoulou K, Wszolek Z, Chase B, Taka H, Mineki R, Murayama K, Riess O, Mizuno Y, Hattori N. Kobayashi H, et al. Among authors: riess o. Brain. 2003 Jan;126(Pt 1):32-42. doi: 10.1093/brain/awg010. Brain. 2003. PMID: 12477695

4

14-3-3 protein is a component of Lewy bodies in Parkinson's disease-mutation analysis and association studies of 14-3-3 eta.

Ubl A, Berg D, Holzmann C, Krüger R, Berger K, Arzberger T, Bornemann A, Riess O. Ubl A, et al. Among authors: riess o. Brain Res Mol Brain Res. 2002 Dec;108(1-2):33-9. doi: 10.1016/s0169-328x(02)00510-7. Brain Res Mol Brain Res. 2002. PMID: 12480176

5

Spectrum of phenotypes and genotypes in Parkinson's disease.

Riess O, Krüger R, Schulz JB. Riess O, et al. J Neurol. 2002 Oct;249 Suppl 3:III/15-20. doi: 10.1007/s00415-002-1303-2. J Neurol. 2002. PMID: 12522566 Review.

6

Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease.

Marx FP, Holzmann C, Strauss KM, Li L, Eberhardt O, Gerhardt E, Cookson MR, Hernandez D, Farrer MJ, Kachergus J, Engelender S, Ross CA, Berger K, Schöls L, Schulz JB, Riess O, Krüger R. Marx FP, et al. Among authors: riess o. Hum Mol Genet. 2003 Jun 1;12(11):1223-31. doi: 10.1093/hmg/ddg134. Hum Mol Genet. 2003. PMID: 12761037

7

Therapeutic strategies for Parkinson's disease based on data derived from genetic research.

Riess O, Berg D, Krüger R, Schulz JB. Riess O, et al. J Neurol. 2003 Feb;250 Suppl 1:I3-10. doi: 10.1007/s00415-003-1101-3. J Neurol. 2003. PMID: 12761628 Review.

8

Specification of 14-3-3 proteins in Lewy bodies.

Berg D, Riess O, Bornemann A. Berg D, et al. Among authors: riess o. Ann Neurol. 2003 Jul;54(1):135. doi: 10.1002/ana.10621. Ann Neurol. 2003. PMID: 12838532 No abstract available.

9

14-3-3 proteins in the nervous system.

Berg D, Holzmann C, Riess O. Berg D, et al. Among authors: riess o. Nat Rev Neurosci. 2003 Sep;4(9):752-62. doi: 10.1038/nrn1197. Nat Rev Neurosci. 2003. PMID: 12951567 Review. No abstract available.

10

Mutation analysis of the neurofilament M gene in Parkinson's disease.

Krüger R, Fischer C, Schulte T, Strauss KM, Müller T, Woitalla D, Berg D, Hungs M, Gobbele R, Berger K, Epplen JT, Riess O, Schöls L. Krüger R, et al. Among authors: riess o. Neurosci Lett. 2003 Nov 13;351(2):125-9. doi: 10.1016/s0304-3940(03)00903-0. Neurosci Lett. 2003. PMID: 14583397

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