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Huntington disease alters the actionable information in plasma extracellular vesicles.
Neueder A, Nitzschner P, Wagner R, Hummel J, Hoschek F, Wagner M, Abdelmoez A, von Einem B, Landwehrmeyer GB, Tabrizi SJ, Orth M. Neueder A, et al. Among authors: landwehrmeyer gb. Clin Transl Med. 2024 Jan;14(1):e1525. doi: 10.1002/ctm2.1525. Clin Transl Med. 2024. PMID: 38193625 Free PMC article. No abstract available.
An exploratory double-blind, randomized clinical trial with selisistat, a SirT1 inhibitor, in patients with Huntington's disease.
Süssmuth SD, Haider S, Landwehrmeyer GB, Farmer R, Frost C, Tripepi G, Andersen CA, Di Bacco M, Lamanna C, Diodato E, Massai L, Diamanti D, Mori E, Magnoni L, Dreyhaupt J, Schiefele K, Craufurd D, Saft C, Rudzinska M, Ryglewicz D, Orth M, Brzozy S, Baran A, Pollio G, Andre R, Tabrizi SJ, Darpo B, Westerberg G; PADDINGTON Consortium. Süssmuth SD, et al. Among authors: landwehrmeyer gb. Br J Clin Pharmacol. 2015 Mar;79(3):465-76. doi: 10.1111/bcp.12512. Br J Clin Pharmacol. 2015. PMID: 25223731 Free PMC article. Clinical Trial.
Impact of the control for corrupted diffusion tensor imaging data in comparisons at the group level: an application in Huntington disease.
Müller HP, Kassubek J, Grön G, Sprengelmeyer R, Ludolph AC, Klöppel S, Hobbs NZ, Roos RA, Duerr A, Tabrizi SJ, Orth M, Süssmuth SD, Landwehrmeyer GB. Müller HP, et al. Among authors: landwehrmeyer gb. Biomed Eng Online. 2014 Sep 1;13:128. doi: 10.1186/1475-925X-13-128. Biomed Eng Online. 2014. PMID: 25178314 Free PMC article.
Observing Huntington's Disease: the European Huntington's Disease Network's REGISTRY.
Orth M, Handley OJ, Schwenke C, Dunnett SB, Craufurd D, Ho AK, Wild E, Tabrizi SJ, Landwehrmeyer GB; Investigators of the European Huntington's Disease Network. Orth M, et al. Among authors: landwehrmeyer gb. PLoS Curr. 2010 Sep 28;2:RRN1184. doi: 10.1371/currents.RRN1184. PLoS Curr. 2010. PMID: 20890398 Free PMC article.
Identification of extreme motor phenotypes in Huntington's disease.
Braisch U, Hay B, Muche R, Rothenbacher D, Landwehrmeyer GB, Long JD, Orth M; REGISTRY Investigators of the European Huntington's Disease Network and COHORT Investigators of the Huntington Study Group. Braisch U, et al. Among authors: landwehrmeyer gb. Am J Med Genet B Neuropsychiatr Genet. 2017 Apr;174(3):283-294. doi: 10.1002/ajmg.b.32514. Epub 2016 Nov 21. Am J Med Genet B Neuropsychiatr Genet. 2017. PMID: 27868347
Defining pediatric huntington disease: Time to abandon the term Juvenile Huntington Disease?
Quarrell OWJ, Nance MA, Nopoulos P, Reilmann R, Oosterloo M, Tabrizi SJ, Furby H, Saft C, Roos RAC, Squitieri F, Landwehrmeyer GB, Burgunder JM; Juvenile Huntington Disease Working Group of the European Huntington Disease Network. Quarrell OWJ, et al. Among authors: landwehrmeyer gb. Mov Disord. 2019 Apr;34(4):584-585. doi: 10.1002/mds.27640. Epub 2019 Feb 20. Mov Disord. 2019. PMID: 30788860 No abstract available.
Identification of symbol digit modality test score extremes in Huntington's disease.
Braisch U, Muche R, Rothenbacher D, Landwehrmeyer GB, Long JD, Orth M; REGISTRY Investigators of the European Huntington's Disease Network and COHORT Investigators of the Huntington Study Group. Braisch U, et al. Among authors: landwehrmeyer gb. Am J Med Genet B Neuropsychiatr Genet. 2019 Apr;180(3):232-245. doi: 10.1002/ajmg.b.32719. Epub 2019 Feb 20. Am J Med Genet B Neuropsychiatr Genet. 2019. PMID: 30788902
176 results