Schulte C - Search Results

1

No association between Parkinson disease and autoantibodies against NMDA-type glutamate receptors.

Hopfner F, Müller SH, Steppat D, Miller J, Schmidt N, Wandinger KP, Leypoldt F, Berg D, Franke A, Lieb W, Tittmann L, Balzer-Geldsetzer M, Baudrexel S, Dodel R, Hilker-Roggendorf R, Kalbe E, Kassubek J, Klockgether T, Liepelt-Scarfone I, Mollenhauer B, Neuser P, Reetz K, Riedel O, Schulte C, Schulz JB, Spottke A, Storch A, Trenkwalder C, Wittchen HU, Witt K, Wüllner U, Deuschl G, Kuhlenbäumer G. Hopfner F, et al. Among authors: schulte c. Transl Neurodegener. 2019 Apr 3;8:11. doi: 10.1186/s40035-019-0153-0. eCollection 2019. Transl Neurodegener. 2019. PMID: 30984390 Free PMC article.

2

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

3

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

4

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

5

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

6

Polymorphisms in TGFB1 and PDGFRB are associated with Moyamoya disease in European patients.

Roder C, Peters V, Kasuya H, Nishizawa T, Takehara Y, Berg D, Schulte C, Khan N, Tatagiba M, Krischek B. Roder C, et al. Among authors: schulte c. Acta Neurochir (Wien). 2010 Dec;152(12):2153-60. doi: 10.1007/s00701-010-0711-9. Epub 2010 Jun 23. Acta Neurochir (Wien). 2010. PMID: 20571834

7

Analysis of ACTA2 in European Moyamoya disease patients.

Roder C, Peters V, Kasuya H, Nishizawa T, Wakita S, Berg D, Schulte C, Khan N, Tatagiba M, Krischek B. Roder C, et al. Among authors: schulte c. Eur J Paediatr Neurol. 2011 Mar;15(2):117-22. doi: 10.1016/j.ejpn.2010.09.002. Epub 2010 Oct 20. Eur J Paediatr Neurol. 2011. PMID: 20970362

8

Serum and cerebrospinal fluid uric acid levels in lewy body disorders: associations with disease occurrence and amyloid-β pathway.

Maetzler W, Stapf AK, Schulte C, Hauser AK, Lerche S, Wurster I, Schleicher E, Melms A, Berg D. Maetzler W, et al. Among authors: schulte c. J Alzheimers Dis. 2011;27(1):119-26. doi: 10.3233/JAD-2011-110587. J Alzheimers Dis. 2011. PMID: 21765209

9

Analysis of TGFB1 in European and Japanese Moyamoya disease patients.

Liu C, Roder C, Schulte C, Kasuya H, Akagawa H, Nishizawa T, Yoneyama T, Okada Y, Khan N, Tatagiba M, Berg D, Krischek B. Liu C, et al. Among authors: schulte c. Eur J Med Genet. 2012 Oct;55(10):531-4. doi: 10.1016/j.ejmg.2012.05.002. Epub 2012 Jun 1. Eur J Med Genet. 2012. PMID: 22659181

10

GBA-associated PD. Neurodegeneration, altered membrane metabolism, and lack of energy failure.

Brockmann K, Hilker R, Pilatus U, Baudrexel S, Srulijes K, Magerkurth J, Hauser AK, Schulte C, Csoti I, Merten CD, Gasser T, Berg D, Hattingen E. Brockmann K, et al. Among authors: schulte c. Neurology. 2012 Jul 17;79(3):213-20. doi: 10.1212/WNL.0b013e31825dd369. Epub 2012 Jun 20. Neurology. 2012. PMID: 22722629

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