Gasser T - Search Results

1

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

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

2

Inherited myoclonus-dystonia.

Asmus F, Gasser T. Asmus F, et al. Among authors: gasser t. Adv Neurol. 2004;94:113-9. Adv Neurol. 2004. PMID: 14509663 Review. No abstract available.

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

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.

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

Acute parkinsonism with corresponding lesions in the basal ganglia after heroin abuse.

Mätzler W, Nägele T, Gasser T, Krüger R. Mätzler W, et al. Among authors: gasser t. Neurology. 2007 Feb 6;68(6):414. doi: 10.1212/01.wnl.0000250230.86581.ea. Neurology. 2007. PMID: 17283314 No abstract available.

8

Transcranial ultrasound in different monogenetic subtypes of Parkinson's disease.

Schweitzer KJ, Brüssel T, Leitner P, Krüger R, Bauer P, Woitalla D, Tomiuk J, Gasser T, Berg D. Schweitzer KJ, et al. Among authors: gasser t. J Neurol. 2007 May;254(5):613-6. doi: 10.1007/s00415-006-0369-7. Epub 2007 Apr 6. J Neurol. 2007. PMID: 17415511

9

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

10

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

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