Riess O - Search Results

1

Screening for mutations of the IRP2 gene in Parkinson's disease patients with hyperechogenicity of the substantia nigra.

Deplazes J, Schöbel K, Hochstrasser H, Bauer P, Walter U, Behnke S, Spiegel J, Becker G, Riess O, Berg D. Deplazes J, et al. Among authors: riess o. J Neural Transm (Vienna). 2004 Apr;111(4):515-21. doi: 10.1007/s00702-004-0125-z. J Neural Transm (Vienna). 2004. PMID: 15057521

2

Screening for mutations in synaptotagmin XI in Parkinson's disease.

Glass AS, Huynh DP, Franck T, Woitalla D, Müller T, Pulst SM, Berg D, Krüger R, Riess O. Glass AS, et al. Among authors: riess o. J Neural Transm Suppl. 2004;(68):21-8. doi: 10.1007/978-3-7091-0579-5_3. J Neural Transm Suppl. 2004. PMID: 15354386

3

Ceruloplasmin gene variations and substantia nigra hyperechogenicity in Parkinson disease.

Hochstrasser H, Bauer P, Walter U, Behnke S, Spiegel J, Csoti I, Zeiler B, Bornemann A, Pahnke J, Becker G, Riess O, Berg D. Hochstrasser H, et al. Among authors: riess o. Neurology. 2004 Nov 23;63(10):1912-7. doi: 10.1212/01.wnl.0000144276.29988.c3. Neurology. 2004. PMID: 15557511

4

The role of alpha-synuclein gene multiplications in early-onset Parkinson's disease and dementia with Lewy bodies.

Hofer A, Berg D, Asmus F, Niwar M, Ransmayr G, Riemenschneider M, Bonelli SB, Steffelbauer M, Ceballos-Baumann A, Haussermann P, Behnke S, Krüger R, Prestel J, Sharma M, Zimprich A, Riess O, Gasser T. Hofer A, et al. Among authors: riess o. J Neural Transm (Vienna). 2005 Sep;112(9):1249-54. doi: 10.1007/s00702-004-0263-3. Epub 2004 Dec 29. J Neural Transm (Vienna). 2005. PMID: 15622440

5

Genetic causes of Parkinson's disease: extending the pathway.

Riess O, Krüger R, Hochstrasser H, Soehn AS, Nuber S, Franck T, Berg D. Riess O, et al. J Neural Transm Suppl. 2006;(70):181-9. doi: 10.1007/978-3-211-45295-0_29. J Neural Transm Suppl. 2006. PMID: 17017528 Review.

6

Mutation analysis and association studies of the UCHL1 gene in German Parkinson's disease patients.

Wintermeyer P, Krüger R, Kuhn W, Müller T, Woitalla D, Berg D, Becker G, Leroy E, Polymeropoulos M, Berger K, Przuntek H, Schöls L, Epplen JT, Riess O. Wintermeyer P, et al. Among authors: riess o. Neuroreport. 2000 Jul 14;11(10):2079-82. doi: 10.1097/00001756-200007140-00004. Neuroreport. 2000. PMID: 10923647

7

Genetic analysis of immunomodulating factors in sporadic Parkinson's disease.

Krüger R, Hardt C, Tschentscher F, Jäckel S, Kuhn W, Müller T, Werner J, Woitalla D, Berg D, Kühnl N, Fuchs GA, Santos EJ, Przuntek H, Epplen JT, Schöls L, Riess O. Krüger R, et al. Among authors: riess o. J Neural Transm (Vienna). 2000;107(5):553-62. doi: 10.1007/s007020070078. J Neural Transm (Vienna). 2000. PMID: 11072751

8

Mutation analysis and association studies of nuclear factor-kappaB1 in sporadic Parkinson's disease patients.

Wintermeyer P, Riess O, Schöls L, Przuntek H, Miterski B, Epplen JT, Krüger R. Wintermeyer P, et al. Among authors: riess o. J Neural Transm (Vienna). 2002 Sep;109(9):1181-8. doi: 10.1007/s00702-001-0688-x. J Neural Transm (Vienna). 2002. PMID: 12203044

9

Modulation of disease risk according to a cathepsin D / apolipoprotein E genotype in Parkinson's disease.

Schulte T, Böhringer S, Schöls L, Müller T, Fischer C, Riess O, Przuntek H, Berger K, Epplen JT, Krüger R. Schulte T, et al. Among authors: riess o. J Neural Transm (Vienna). 2003 Jul;110(7):749-55. doi: 10.1007/s00702-003-0832-x. J Neural Transm (Vienna). 2003. PMID: 12811635

10

Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson disease.

Hering R, Petrovic S, Mietz EM, Holzmann C, Berg D, Bauer P, Woitalla D, Müller T, Berger K, Krüger R, Riess O. Hering R, et al. Among authors: riess o. Neurology. 2004 Apr 13;62(7):1231-2. doi: 10.1212/01.wnl.0000118285.18383.90. Neurology. 2004. PMID: 15079038 No abstract available.

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