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Query Trace: Tremor and C9orf72[original query]

Role of MAPT in Pure Motor Neuron Disease: Report of a Recurrent Mutation in Italian Patients. Neuro-degenerative diseases 2019 Mar 18 (5-6): 310-314. Origone Paola, Geroldi Alessandro, Lamp Merit, Sanguineri Francesca, Caponnetto Claudia, Cabona Corrado, Gotta Fabio, Trevisan Lucia, Bellone Emilia, Manganelli Fiore, Devigili Grazia, Mandich Pao Similar articles in PubMed
C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies. Neurology 2014 Jan 82 (4): 292-9. Hensman Moss Davina J, Poulter Mark, Beck Jon, Hehir Jason, Polke James M, Campbell Tracy, Adamson Garry, Mudanohwo Ese, McColgan Peter, Haworth Andrea, Wild Edward J, Sweeney Mary G, Houlden Henry, Mead Simon, Tabrizi Sarah Similar articles in PubMed
C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson disease. Annals of human genetics 2013 Sep 77 (5): 351-63. Nuytemans Karen, Bademci Güney, Kohli Martin M, Beecham Gary W, Wang Liyong, Young Juan I, Nahab Fatta, Martin Eden R, Gilbert John R, Benatar Michael, Haines Jonathan L, Scott William K, Züchner Stephan, Pericak-Vance Margaret A, Vance Jeffery Similar articles in PubMed
CGG-repeat expansion in FMR1 is not associated with amyotrophic lateral sclerosis. Neurobiology of aging 2012 Aug 33 (8): 1852.e1-3. Groen Ewout J N, van Rheenen Wouter, Koppers Max, van Doormaal Perry T C, Vlam Lotte, Diekstra Frank P, Dooijes Dennis, Pasterkamp R Jeroen, van den Berg Leonard H, Veldink Jan Similar articles in PubMed