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Page 1
Validation of the QUEST for German-speaking countries.
Hopfner F, Nebel A, Lyons KE, Tröster AI, Kuhlenbäumer G, Deuschl G, Martinez-Martin P. Hopfner F, et al. Among authors: kuhlenbaumer g. Int J Neurosci. 2016;126(2):127-34. doi: 10.3109/00207454.2015.1077241. Epub 2015 Aug 25. Int J Neurosci. 2016. PMID: 26327253
LINGO1 polymorphisms are associated with essential tremor in Europeans.
Thier S, Lorenz D, Nothnagel M, Stevanin G, Dürr A, Nebel A, Schreiber S, Kuhlenbäumer G, Deuschl G, Klebe S. Thier S, et al. Among authors: kuhlenbaumer g. Mov Disord. 2010 Apr 30;25(6):717-23. doi: 10.1002/mds.22887. Mov Disord. 2010. PMID: 20310002
LINGO1 is not associated with Parkinson's disease in German patients.
Klebe S, Thier S, Lorenz D, Nothnagel M, Schreiber S, Klein C, Hagenah J, Kasten M, Berg D, Srulijes K, Gasser T, Deuschl G, Kuhlenbäumer G. Klebe S, et al. Among authors: kuhlenbaumer g. Am J Med Genet B Neuropsychiatr Genet. 2010 Sep;153B(6):1173-8. doi: 10.1002/ajmg.b.31085. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 20468067
Polymorphisms in the glial glutamate transporter SLC1A2 are associated with essential tremor.
Thier S, Lorenz D, Nothnagel M, Poremba C, Papengut F, Appenzeller S, Paschen S, Hofschulte F, Hussl AC, Hering S, Poewe W, Asmus F, Gasser T, Schöls L, Christensen K, Nebel A, Schreiber S, Klebe S, Deuschl G, Kuhlenbäumer G. Thier S, et al. Among authors: kuhlenbaumer g. Neurology. 2012 Jul 17;79(3):243-8. doi: 10.1212/WNL.0b013e31825fdeed. Epub 2012 Jul 3. Neurology. 2012. PMID: 22764253 Free PMC article.
No association between NOD2 variants and Parkinson's disease.
Appenzeller S, Thier S, Papengut F, Klein C, Hagenah J, Kasten M, Berg D, Srulijes K, Gasser T, Schreiber S, Deuschl G, Kuhlenbäumer G. Appenzeller S, et al. Among authors: kuhlenbaumer g. Mov Disord. 2012 Aug;27(9):1191-2. doi: 10.1002/mds.25059. Epub 2012 Jul 13. Mov Disord. 2012. PMID: 22807259 No abstract available.
No association between polymorphisms in the glutamate transporter SLC1A2 and Parkinson's disease.
Appenzeller S, Schulte C, Thier S, Hopfner F, Pendziwiat M, Papengut F, Klein C, Hagenah J, Kasten M, Srulijes K, Berg D, Gasser T, Singleton A, Deuschl G, Kuhlenbäumer G. Appenzeller S, et al. Among authors: kuhlenbaumer g. Mov Disord. 2013 Aug;28(9):1305-6. doi: 10.1002/mds.25330. Epub 2013 Feb 6. Mov Disord. 2013. PMID: 23390085 Free PMC article. No abstract available.
The role of SCARB2 as susceptibility factor in Parkinson's disease.
Hopfner F, Schulte EC, Mollenhauer B, Bereznai B, Knauf F, Lichtner P, Zimprich A, Haubenberger D, Pirker W, Brücke T, Peters A, Gieger C, Kuhlenbäumer G, Trenkwalder C, Winkelmann J. Hopfner F, et al. Among authors: kuhlenbaumer g. Mov Disord. 2013 Apr;28(4):538-40. doi: 10.1002/mds.25349. Epub 2013 Feb 13. Mov Disord. 2013. PMID: 23408458
Rare variants in ANO3 are not a susceptibility factor in essential tremor.
Hopfner F, Bungeroth M, Pendziwiat M, Tittmann L, Deuschl G, Schneider SA, Kuhlenbäumer G. Hopfner F, et al. Among authors: kuhlenbaumer g. Parkinsonism Relat Disord. 2014 Jan;20(1):134-5. doi: 10.1016/j.parkreldis.2013.09.022. Epub 2013 Sep 27. Parkinsonism Relat Disord. 2014. PMID: 24094724 No abstract available.
Genetics of essential tremor: meta-analysis and review.
Kuhlenbäumer G, Hopfner F, Deuschl G. Kuhlenbäumer G, et al. Neurology. 2014 Mar 18;82(11):1000-7. doi: 10.1212/WNL.0000000000000211. Epub 2014 Feb 14. Neurology. 2014. PMID: 24532269 Review.
164 results