Gasser T - Search Results

1

Predictive value of transcranial sonography in the diagnosis of Parkinson's disease.

Prestel J, Schweitzer KJ, Hofer A, Gasser T, Berg D. Prestel J, et al. Among authors: gasser t. Mov Disord. 2006 Oct;21(10):1763-5. doi: 10.1002/mds.21054. Mov Disord. 2006. PMID: 16874758 Clinical Trial.

2

PARK11 is not linked with Parkinson's disease in European families.

Prestel J, Sharma M, Leitner P, Zimprich A, Vaughan JR, Dürr A, Bonifati V, De Michele G, Hanagasi HA, Farrer M, Hofer A, Asmus F, Volpe G, Meco G, Brice A, Wood NW, Müller-Myhsok B, Gasser T; European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD). Prestel J, et al. Among authors: gasser t. Eur J Hum Genet. 2005 Feb;13(2):193-7. doi: 10.1038/sj.ejhg.5201317. Eur J Hum Genet. 2005. PMID: 15523496

3

New aspects of genetic contributions to Parkinson's disease.

Hofer A, Gasser T. Hofer A, et al. Among authors: gasser t. J Mol Neurosci. 2004;24(3):417-24. doi: 10.1385/JMN:24:3:417. J Mol Neurosci. 2004. PMID: 15655263 Review.

4

Multiple regions of alpha-synuclein are associated with Parkinson's disease.

Mueller JC, Fuchs J, Hofer A, Zimprich A, Lichtner P, Illig T, Berg D, Wüllner U, Meitinger T, Gasser T. Mueller JC, et al. Among authors: gasser t. Ann Neurol. 2005 Apr;57(4):535-41. doi: 10.1002/ana.20438. Ann Neurol. 2005. PMID: 15786467

5

Alpha-synuclein and Parkinson's disease: implications from the screening of more than 1,900 patients.

Berg D, Niwar M, Maass S, Zimprich A, Möller JC, Wuellner U, Schmitz-Hübsch T, Klein C, Tan EK, Schöls L, Marsh L, Dawson TM, Janetzky B, Müller T, Woitalla D, Kostic V, Pramstaller PP, Oertel WH, Bauer P, Krueger R, Gasser T, Riess O. Berg D, et al. Among authors: gasser t. Mov Disord. 2005 Sep;20(9):1191-4. doi: 10.1002/mds.20504. Mov Disord. 2005. PMID: 15895422

6

Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease.

Strauss KM, Martins LM, Plun-Favreau H, Marx FP, Kautzmann S, Berg D, Gasser T, Wszolek Z, Müller T, Bornemann A, Wolburg H, Downward J, Riess O, Schulz JB, Krüger R. Strauss KM, et al. Among authors: gasser t. Hum Mol Genet. 2005 Aug 1;14(15):2099-111. doi: 10.1093/hmg/ddi215. Epub 2005 Jun 16. Hum Mol Genet. 2005. PMID: 15961413

7

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: gasser t. Brain. 2005 Dec;128(Pt 12):3000-11. doi: 10.1093/brain/awh666. Brain. 2005. PMID: 16251215 No abstract available.

8

Common variants of LRRK2 are not associated with sporadic Parkinson's disease.

Biskup S, Mueller JC, Sharma M, Lichtner P, Zimprich A, Berg D, Wüllner U, Illig T, Meitinger T, Gasser T. Biskup S, et al. Among authors: gasser t. Ann Neurol. 2005 Dec;58(6):905-8. doi: 10.1002/ana.20664. Ann Neurol. 2005. PMID: 16254973

9

Osteopontin is elevated in Parkinson's disease and its absence leads to reduced neurodegeneration in the MPTP model.

Maetzler W, Berg D, Schalamberidze N, Melms A, Schott K, Mueller JC, Liaw L, Gasser T, Nitsch C. Maetzler W, et al. Among authors: gasser t. Neurobiol Dis. 2007 Mar;25(3):473-82. doi: 10.1016/j.nbd.2006.10.020. Epub 2006 Dec 26. Neurobiol Dis. 2007. PMID: 17188882

10

Data protection in biomaterial banks for Parkinson's disease research: the model of GEPARD (Gene Bank Parkinson's Disease Germany).

Eggert K, Wüllner U, Antony G, Gasser T, Janetzky B, Klein C, Schöls L, Oertel W. Eggert K, et al. Among authors: gasser t. Mov Disord. 2007 Apr 15;22(5):611-8. doi: 10.1002/mds.21331. Mov Disord. 2007. PMID: 17230444

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