Schulte C - Search Results

1

Parkinson's disease: evolution of cognitive impairment and CSF Aβ_1-42 profiles in a prospective longitudinal study.

Lerche S, Wurster I, Röben B, Machetanz G, Zimmermann M, Bernhard F, Stransky E, Deuschle C, Schulte C, Hansson O, Zetterberg H, Gasser T, Berg D, Maetzler W, Brockmann K. Lerche S, et al. Among authors: schulte c. J Neurol Neurosurg Psychiatry. 2019 Feb;90(2):165-170. doi: 10.1136/jnnp-2018-318956. Epub 2018 Sep 25. J Neurol Neurosurg Psychiatry. 2019. PMID: 30254084

2

Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*.

Berg D, Schweitzer KJ, Leitner P, Zimprich A, Lichtner P, Belcredi P, Brüssel T, Schulte C, Maass S, Nägele T, Wszolek ZK, Gasser T. Berg D, et al. Among authors: schulte c. Brain. 2005 Dec;128(Pt 12):3000-11. doi: 10.1093/brain/awh666. Brain. 2005. PMID: 16251215 No abstract available.

3

The transcription factor PITX3 is associated with sporadic Parkinson's disease.

Fuchs J, Mueller JC, Lichtner P, Schulte C, Munz M, Berg D, Wüllner U, Illig T, Sharma M, Gasser T. Fuchs J, et al. Among authors: schulte c. Neurobiol Aging. 2009 May;30(5):731-8. doi: 10.1016/j.neurobiolaging.2007.08.014. Epub 2007 Oct 1. Neurobiol Aging. 2009. PMID: 17905480

4

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: schulte c. 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

5

Cortical PIB binding in Lewy body disease is associated with Alzheimer-like characteristics.

Maetzler W, Liepelt I, Reimold M, Reischl G, Solbach C, Becker C, Schulte C, Leyhe T, Keller S, Melms A, Gasser T, Berg D. Maetzler W, et al. Among authors: schulte c. Neurobiol Dis. 2009 Apr;34(1):107-12. doi: 10.1016/j.nbd.2008.12.008. Epub 2008 Dec 31. Neurobiol Dis. 2009. PMID: 19162186

6

A single-nucleotide polymorphism of the osteopontin gene may contribute to a susceptibility to Lewy body disease.

Maetzler W, Michelis J, Tomiuk J, Melms A, Becker C, Gasser T, Schulte C, Berg D. Maetzler W, et al. Among authors: schulte c. J Neural Transm (Vienna). 2009 May;116(5):599-605. doi: 10.1007/s00702-009-0209-x. Epub 2009 Apr 2. J Neural Transm (Vienna). 2009. PMID: 19340392

7

Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease: large-scale collaborative study.

Evangelou E, Maraganore DM, Annesi G, Brighina L, Brice A, Elbaz A, Ferrarese C, Hadjigeorgiou GM, Krueger R, Lambert JC, Lesage S, Markopoulou K, Mellick GD, Meeus B, Pedersen NL, Quattrone A, Van Broeckhoven C, Sharma M, Silburn PA, Tan EK, Wirdefeldt K, Ioannidis JP; Genetic Epidemiology of Parkinson's Disease (GEOPD) Consortium. Evangelou E, et al. Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 5;153B(1):220-8. doi: 10.1002/ajmg.b.30980. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19475631 Free PMC article.

8

No differences of butyrylcholinesterase protein activity and allele frequency in Lewy body diseases.

Maetzler W, Keller S, Michelis J, Koehler N, Stransky E, Becker C, Schulte C, Melms A, Gasser T, Berg D. Maetzler W, et al. Among authors: schulte c. Neurobiol Dis. 2009 Aug;35(2):296-301. doi: 10.1016/j.nbd.2009.05.014. Epub 2009 May 27. Neurobiol Dis. 2009. PMID: 19481150

9

Effect of genetic variation in Kv1.3 on olfactory function.

Guthoff M, Tschritter O, Berg D, Liepelt I, Schulte C, Machicao F, Haering HU, Fritsche A. Guthoff M, et al. Among authors: schulte c. Diabetes Metab Res Rev. 2009 Sep;25(6):523-7. doi: 10.1002/dmrr.979. Diabetes Metab Res Rev. 2009. PMID: 19489042

10

Ataxia with ophthalmoplegia or sensory neuropathy is frequently caused by POLG mutations.

Schulte C, Synofzik M, Gasser T, Schöls L. Schulte C, et al. Neurology. 2009 Sep 15;73(11):898-900. doi: 10.1212/WNL.0b013e3181b78488. Neurology. 2009. PMID: 19752458 No abstract available.

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