Gasser T - Search Results

1

Lack of association between the interleukin-1 alpha (-889) polymorphism and early-onset Parkinson's disease.

Möller JC, Depboylu C, Kölsch H, Lohmüller F, Bandmann O, Gocke P, Du Y, Paus S, Wüllner U, Gasser T, Oertel WH, Klockgether T, Dodel RC. Möller JC, et al. Among authors: gasser t. Neurosci Lett. 2004 Apr 15;359(3):195-7. doi: 10.1016/j.neulet.2004.01.058. Neurosci Lett. 2004. PMID: 15050696 Clinical Trial.

2

State of the art review: molecular diagnosis of inherited movement disorders. Movement Disorders Society task force on molecular diagnosis.

Gasser T, Bressman S, Dürr A, Higgins J, Klockgether T, Myers RH. Gasser T, et al. Mov Disord. 2003 Jan;18(1):3-18. doi: 10.1002/mds.10338. Mov Disord. 2003. PMID: 12518296 Review.

3

Lack of association of interleukin-10 promoter region polymorphisms with Alzheimer's disease.

Depboylu C, Du Y, Müller U, Kurz A, Zimmer R, Riemenschneider M, Gasser T, Oertel WH, Klockgether T, Dodel RC. Depboylu C, et al. Among authors: gasser t. Neurosci Lett. 2003 May 15;342(1-2):132-4. doi: 10.1016/s0304-3940(03)00231-3. Neurosci Lett. 2003. PMID: 12727335

4

An interleukin-6 promoter variant is not associated with an increased risk for Alzheimer's disease.

Depboylu C, Lohmüller F, Gocke P, Du Y, Zimmer R, Gasser T, Klockgether T, Dodel RC. Depboylu C, et al. Among authors: gasser t. Dement Geriatr Cogn Disord. 2004;17(3):170-3. doi: 10.1159/000076352. Epub 2004 Jan 20. Dement Geriatr Cogn Disord. 2004. PMID: 14739540

5

A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample.

Buervenich S, Carmine A, Galter D, Shahabi HN, Johnels B, Holmberg B, Ahlberg J, Nissbrandt H, Eerola J, Hellström O, Tienari PJ, Matsuura T, Ashizawa T, Wüllner U, Klockgether T, Zimprich A, Gasser T, Hanson M, Waseem S, Singleton A, McMahon FJ, Anvret M, Sydow O, Olson L. Buervenich S, et al. Among authors: gasser t. Arch Neurol. 2005 Jan;62(1):74-8. doi: 10.1001/archneur.62.1.74. Arch Neurol. 2005. PMID: 15642852

6

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

7

Mutations in the pantothenate kinase gene PANK2 are not associated with Parkinson disease.

Klopstock T, Elstner M, Lücking CB, Müller-Myhsok B, Gasser T, Botz E, Lichtner P, Hörtnagel K. Klopstock T, et al. Among authors: gasser t. Neurosci Lett. 2005 May 13;379(3):195-8. doi: 10.1016/j.neulet.2004.12.061. Neurosci Lett. 2005. PMID: 15843062

8

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

9

UCHL-1 gene in multiple system atrophy: a haplotype tagging approach.

Healy DG, Abou-Sleiman PM, Quinn N, Ahmadi KR, Ozawa T, Kamm C, Wullner U, Oertel WH, Burk K, Dupont E, Pellecchia MT, Tolosa E, Gasser T, Holton JL, Revesz T, Goldstein DB, Lees AJ, Wood NW; European MSA Study Group. Healy DG, et al. Among authors: gasser t. Mov Disord. 2005 Oct;20(10):1338-43. doi: 10.1002/mds.20575. Mov Disord. 2005. PMID: 16007636

10

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

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