Epplen JT - Search Results

1

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: epplen jt. Neuroreport. 2000 Aug 3;11(11):2439-42. doi: 10.1097/00001756-200008030-00020. Neuroreport. 2000. PMID: 10943700

2

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: epplen jt. Neurosci Lett. 2003 Nov 13;351(2):125-9. doi: 10.1016/s0304-3940(03)00903-0. Neurosci Lett. 2003. PMID: 14583397

3

Analysis of the parkin deletion in sporadic and familial Parkinson's disease. Short communication.

Krüger R, Vieira-Säcker AM, Kuhn W, Müller T, Woitalla D, Schöls L, Przuntek H, Epplen JT, Riess O. Krüger R, et al. Among authors: epplen jt. J Neural Transm (Vienna). 1999;106(2):159-63. doi: 10.1007/s007020050148. J Neural Transm (Vienna). 1999. PMID: 10226936

4

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: epplen jt. 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

5

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: epplen jt. Neuroreport. 2000 Jul 14;11(10):2079-82. doi: 10.1097/00001756-200007140-00004. Neuroreport. 2000. PMID: 10923647

6

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: epplen jt. J Neural Transm (Vienna). 2000;107(5):553-62. doi: 10.1007/s007020070078. J Neural Transm (Vienna). 2000. PMID: 11072751

7

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: epplen jt. Neurosci Lett. 2001 Sep 14;310(2-3):191-3. doi: 10.1016/s0304-3940(01)02127-9. Neurosci Lett. 2001. PMID: 11585599

8

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: epplen jt. J Neural Transm (Vienna). 2003 Jul;110(7):749-55. doi: 10.1007/s00702-003-0832-x. J Neural Transm (Vienna). 2003. PMID: 12811635

9

Parkin gene variations in late-onset Parkinson's disease: comparison between Norwegian and German cohorts.

Schlitter AM, Kurz M, Larsen JP, Woitalla D, Müller T, Epplen JT, Dekomien G. Schlitter AM, et al. Among authors: epplen jt. Acta Neurol Scand. 2006 Jan;113(1):9-13. doi: 10.1111/j.1600-0404.2005.00532.x. Acta Neurol Scand. 2006. PMID: 16367892

10

Relations between genotype and phenotype in German patients with the Machado-Joseph disease mutation.

Schöls L, Amoiridis G, Epplen JT, Langkafel M, Przuntek H, Riess O. Schöls L, et al. Among authors: epplen jt. J Neurol Neurosurg Psychiatry. 1996 Nov;61(5):466-70. doi: 10.1136/jnnp.61.5.466. J Neurol Neurosurg Psychiatry. 1996. PMID: 8937340 Free PMC article.

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