Gasser T - Search Results

1

Rare Variants in Neurodegeneration Associated Genes Revealed by Targeted Panel Sequencing in a German ALS Cohort.

Krüger S, Battke F, Sprecher A, Munz M, Synofzik M, Schöls L, Gasser T, Grehl T, Prudlo J, Biskup S. Krüger S, et al. Among authors: gasser t. Front Mol Neurosci. 2016 Oct 13;9:92. doi: 10.3389/fnmol.2016.00092. eCollection 2016. Front Mol Neurosci. 2016. PMID: 27790088 Free PMC article.

2

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.

Zimprich A, Biskup S, Leitner P, Lichtner P, Farrer M, Lincoln S, Kachergus J, Hulihan M, Uitti RJ, Calne DB, Stoessl AJ, Pfeiffer RF, Patenge N, Carbajal IC, Vieregge P, Asmus F, Müller-Myhsok B, Dickson DW, Meitinger T, Strom TM, Wszolek ZK, Gasser T. Zimprich A, et al. Among authors: gasser t. Neuron. 2004 Nov 18;44(4):601-7. doi: 10.1016/j.neuron.2004.11.005. Neuron. 2004. PMID: 15541309 Free article.

3

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

4

Myoclonus-dystonia due to genomic deletions in the epsilon-sarcoglycan gene.

Asmus F, Salih F, Hjermind LE, Ostergaard K, Munz M, Kühn AA, Dupont E, Kupsch A, Gasser T. Asmus F, et al. Among authors: gasser t. Ann Neurol. 2005 Nov;58(5):792-7. doi: 10.1002/ana.20661. Ann Neurol. 2005. PMID: 16240355

5

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

6

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

7

Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystonia.

Asmus F, Devlin A, Munz M, Zimprich A, Gasser T, Chinnery PF. Asmus F, et al. Among authors: gasser t. Mov Disord. 2007 Oct 31;22(14):2104-9. doi: 10.1002/mds.21692. Mov Disord. 2007. PMID: 17702043

8

Genomic deletion size at the epsilon-sarcoglycan locus determines the clinical phenotype.

Asmus F, Hjermind LE, Dupont E, Wagenstaller J, Haberlandt E, Munz M, Strom TM, Gasser T. Asmus F, et al. Among authors: gasser t. Brain. 2007 Oct;130(Pt 10):2736-45. doi: 10.1093/brain/awm209. Brain. 2007. PMID: 17898012

9

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: gasser t. 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

10

Genetic variability in the SNCA gene influences alpha-synuclein levels in the blood and brain.

Fuchs J, Tichopad A, Golub Y, Munz M, Schweitzer KJ, Wolf B, Berg D, Mueller JC, Gasser T. Fuchs J, et al. Among authors: gasser t. FASEB J. 2008 May;22(5):1327-34. doi: 10.1096/fj.07-9348com. Epub 2007 Dec 27. FASEB J. 2008. PMID: 18162487

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