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Genes associated with Parkinson syndrome.
Biskup S, Gerlach M, Kupsch A, Reichmann H, Riederer P, Vieregge P, Wüllner U, Gasser T. Biskup S, et al. Among authors: wullner u. J Neurol. 2008 Sep;255 Suppl 5:8-17. doi: 10.1007/s00415-008-5005-2. J Neurol. 2008. PMID: 18787878 Review.
New medical and surgical treatments for Parkinson's disease.
Klockgether T, Löschmann PA, Wüllner U. Klockgether T, et al. Among authors: wullner u. Curr Opin Neurol. 1994 Aug;7(4):346-52. doi: 10.1097/00019052-199408000-00012. Curr Opin Neurol. 1994. PMID: 7952244 Review.
Inflammation in Parkinson's disease.
Wüllner U, Klockgether T. Wüllner U, et al. J Neurol. 2003 Feb;250 Suppl 1:I35-8. doi: 10.1007/s00415-003-1107-x. J Neurol. 2003. PMID: 12761634 Review.
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: wullner u. Arch Neurol. 2005 Jan;62(1):74-8. doi: 10.1001/archneur.62.1.74. Arch Neurol. 2005. PMID: 15642852
The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group.
Kamm C, Healy DG, Quinn NP, Wüllner U, Moller JC, Schols L, Geser F, Burk K, Børglum AD, Pellecchia MT, Tolosa E, del Sorbo F, Nilsson C, Bandmann O, Sharma M, Mayer P, Gasteiger M, Haworth A, Ozawa T, Lees AJ, Short J, Giunti P, Holinski-Feder E, Illig T, Wichmann HE, Wenning GK, Wood NW, Gasser T; European Multiple System Atrophy Study Group. Kamm C, et al. Among authors: wullner u. Brain. 2005 Aug;128(Pt 8):1855-60. doi: 10.1093/brain/awh535. Epub 2005 Jun 9. Brain. 2005. PMID: 15947063
253 results