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Acta Neuropathologica Communications|February 4, 2017
Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brainsWei Wei, Michael J Keogh, Ian Wilson, et al.Nature|July 25, 2006
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17Matt Baker, Ian R Mackenzie, Stuart M Pickering-Brown, et al.Neurobiology of Aging|February 17, 2009
Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degenerationSara Rollinson, Patrizia Rizzu, Stephen Sikkink, et al.Neurobiology of Aging|September 20, 2011
Chromosome 9 ALS and FTD locus is probably derived from a single founderKin Mok, Bryan J Traynor, Jennifer Schymick, et al.The Lancet. Oncology|January 4, 2006
Genetic variation in TNF and IL10 and risk of non-Hodgkin lymphoma: a report from the InterLymph ConsortiumNathaniel Rothman, Christine F Skibola, Sophia S Wang, et al.The Lancet. Neurology|March 13, 2012
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional studyElisa Majounie, Alan E Renton, Kin Mok, et al.Neuron|September 28, 2011
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTDAlan E Renton, Elisa Majounie, Adrian Waite, et al.Brain : a Journal of Neurology|September 26, 2018
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriersMing Zhang, Raffaele Ferrari, Maria Carmela Tartaglia, et al.Neuron|May 3, 2024
Genome sequence analyses identify novel risk loci for multiple system atrophyRuth Chia, Anindita Ray, Zalak Shah, et al.Neurology|September 18, 2020
C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohortsBeatrice Costa, Claudia Manzoni, Manuel Bernal-Quiros, et al.Pageof 7