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No association between Parkinson disease and autoantibodies against NMDA-type glutamate receptors.
Hopfner F, Müller SH, Steppat D, Miller J, Schmidt N, Wandinger KP, Leypoldt F, Berg D, Franke A, Lieb W, Tittmann L, Balzer-Geldsetzer M, Baudrexel S, Dodel R, Hilker-Roggendorf R, Kalbe E, Kassubek J, Klockgether T, Liepelt-Scarfone I, Mollenhauer B, Neuser P, Reetz K, Riedel O, Schulte C, Schulz JB, Spottke A, Storch A, Trenkwalder C, Wittchen HU, Witt K, Wüllner U, Deuschl G, Kuhlenbäumer G. Hopfner F, et al. Transl Neurodegener. 2019 Apr 3;8:11. doi: 10.1186/s40035-019-0153-0. eCollection 2019. Transl Neurodegener. 2019. PMID: 30984390 Free PMC article.
Rest tremor revisited: Parkinson's disease and other disorders.
Chen W, Hopfner F, Becktepe JS, Deuschl G. Chen W, et al. Among authors: hopfner f. Transl Neurodegener. 2017 Jun 16;6:16. doi: 10.1186/s40035-017-0086-4. eCollection 2017. Transl Neurodegener. 2017. PMID: 28638597 Free PMC article. Review.
Examination of Patients with Essential Tremor.
Hopfner F, Deuschl G. Hopfner F, et al. Mov Disord Clin Pract. 2014 Apr 10;1(1):87. doi: 10.1002/mdc3.12012. eCollection 2014 Apr. Mov Disord Clin Pract. 2014. PMID: 30838227 Free PMC article.
Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's Disease.
Hopfner F, Mueller SH, Szymczak S, Junge O, Tittmann L, May S, Lohmann K, Grallert H, Lieb W, Strauch K, Müller-Nurasyid M, Berger K, Schormair B, Winkelmann J, Mollenhauer B, Trenkwalder C, Maetzler W, Berg D, Kasten M, Klein C, Höglinger GU, Gasser T, Deuschl G, Franke A, Krawczak M, Dempfle A, Kuhlenbäumer G. Hopfner F, et al. Mov Disord. 2020 Jul;35(7):1245-1248. doi: 10.1002/mds.28037. Epub 2020 Apr 8. Mov Disord. 2020. PMID: 32267580
Private variants in PRKN are associated with late-onset Parkinson's disease.
Hopfner F, Mueller SH, Szymczak S, Junge O, Tittmann L, May S, Lohmann K, Grallert H, Lieb W, Strauch K, Müller-Nurasyid M, Berger K, Schormair B, Winkelmann J, Mollenhauer B, Trenkwalder C, Maetzler W, Berg D, Kasten M, Klein C, Höglinger GU, Gasser T, Deuschl G, Franke A, Krawczak M, Dempfle A, Kuhlenbäumer G. Hopfner F, et al. Parkinsonism Relat Disord. 2020 Jun;75:24-26. doi: 10.1016/j.parkreldis.2020.05.003. Epub 2020 May 11. Parkinsonism Relat Disord. 2020. PMID: 32442813 No abstract available.
Gut microbiota in Parkinson disease in a northern German cohort.
Hopfner F, Künstner A, Müller SH, Künzel S, Zeuner KE, Margraf NG, Deuschl G, Baines JF, Kuhlenbäumer G. Hopfner F, et al. Brain Res. 2017 Jul 15;1667:41-45. doi: 10.1016/j.brainres.2017.04.019. Epub 2017 May 12. Brain Res. 2017. PMID: 28506555
Is essential tremor a single entity?
Hopfner F, Deuschl G. Hopfner F, et al. Eur J Neurol. 2018 Jan;25(1):71-82. doi: 10.1111/ene.13454. Epub 2017 Oct 16. Eur J Neurol. 2018. PMID: 28905504 Review.
[Genetics of tremor].
Kuhlenbäumer G, Hopfner F. Kuhlenbäumer G, et al. Among authors: hopfner f. Nervenarzt. 2018 Apr;89(4):416-422. doi: 10.1007/s00115-017-0478-9. Nervenarzt. 2018. PMID: 29327099 Review. German.
Genetics of essential tremor: meta-analysis and review.
Kuhlenbäumer G, Hopfner F, Deuschl G. Kuhlenbäumer G, et al. Among authors: hopfner f. Neurology. 2014 Mar 18;82(11):1000-7. doi: 10.1212/WNL.0000000000000211. Epub 2014 Feb 14. Neurology. 2014. PMID: 24532269 Review.
Mutations in HTRA2 are not a common cause of familial classic ET.
Hopfner F, Müller SH, Lorenz D, Appenzeller S, Klebe S, Deuschl G, Kuhlenbäumer G. Hopfner F, et al. Mov Disord. 2015 Jul;30(8):1149-50. doi: 10.1002/mds.26252. Epub 2015 May 13. Mov Disord. 2015. PMID: 25970799 No abstract available.
72 results