Riess O - Search Results

1

Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease.

Krüger R, Kuhn W, Müller T, Woitalla D, Graeber M, Kösel S, Przuntek H, Epplen JT, Schöls L, Riess O. Krüger R, et al. Among authors: riess o. Nat Genet. 1998 Feb;18(2):106-8. doi: 10.1038/ng0298-106. Nat Genet. 1998. PMID: 9462735 No abstract available.

2

Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotype.

Krüger R, Vieira-Saecker AM, Kuhn W, Berg D, Müller T, Kühnl N, Fuchs GA, Storch A, Hungs M, Woitalla D, Przuntek H, Epplen JT, Schöls L, Riess O. Krüger R, et al. Among authors: riess o. Ann Neurol. 1999 May;45(5):611-7. doi: 10.1002/1531-8249(199905)45:5<611::aid-ana9>3.0.co;2-x. Ann Neurol. 1999. PMID: 10319883

3

Involvement of alpha-synuclein in Parkinson's disease and other neurodegenerative disorders.

Krüger R, Müller T, Riess O. Krüger R, et al. Among authors: riess o. J Neural Transm (Vienna). 2000;107(1):31-40. doi: 10.1007/s007020050002. J Neural Transm (Vienna). 2000. PMID: 10809401 Review.

4

Genetic influence on the development of Parkinson's disease.

Riess O, Kuhn W, Krüger R. Riess O, et al. J Neurol. 2000 Apr;247 Suppl 2:II69-74. doi: 10.1007/pl00007764. J Neurol. 2000. PMID: 10991669 Review.

5

Familial parkinsonism with synuclein pathology: clinical and PET studies of A30P mutation carriers.

Krüger R, Kuhn W, Leenders KL, Sprengelmeyer R, Müller T, Woitalla D, Portman AT, Maguire RP, Veenma L, Schröder U, Schöls L, Epplen JT, Riess O, Przuntek H. Krüger R, et al. Among authors: riess o. Neurology. 2001 May 22;56(10):1355-62. doi: 10.1212/wnl.56.10.1355. Neurology. 2001. PMID: 11376188

6

Evaluation of the gamma-synuclein gene in German Parkinson's disease patients.

Krüger R, Schöls L, Müller T, Kuhn W, Woitalla D, Przuntek H, Epplen JT, Riess O. Krüger R, et al. Among authors: riess o. Neurosci Lett. 2001 Sep 14;310(2-3):191-3. doi: 10.1016/s0304-3940(01)02127-9. Neurosci Lett. 2001. PMID: 11585599

7

Genetic dissection of familial Parkinson's disease.

Riess O, Jakes R, Krüger R. Riess O, et al. Mol Med Today. 1998 Oct;4(10):438-44. doi: 10.1016/s1357-4310(98)01343-4. Mol Med Today. 1998. PMID: 9793932 Review.

8

Parkinson's disease--a multifactorial neurodegenerative disorder.

Riess O, Krüger R. Riess O, et al. J Neural Transm Suppl. 1999;56:113-25. doi: 10.1007/978-3-7091-6360-3_6. J Neural Transm Suppl. 1999. PMID: 10370906 Review.

9

Genetic analysis of the alpha2-macroglobulin gene in early- and late-onset Parkinson's disease.

Krüger R, Menezes-Saecker AM, Schöls L, Kuhn W, Müller T, Woitalla D, Berg D, Berger K, Przuntek H, Epplen JT, Riess O. Krüger R, et al. Among authors: riess o. Neuroreport. 2000 Aug 3;11(11):2439-42. doi: 10.1097/00001756-200008030-00020. Neuroreport. 2000. PMID: 10943700

10

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

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