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Page 1
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study.
Majounie E, Renton AE, Mok K, Dopper EG, Waite A, Rollinson S, Chiò A, Restagno G, Nicolaou N, Simon-Sanchez J, van Swieten JC, Abramzon Y, Johnson JO, Sendtner M, Pamphlett R, Orrell RW, Mead S, Sidle KC, Houlden H, Rohrer JD, Morrison KE, Pall H, Talbot K, Ansorge O; Chromosome 9-ALS/FTD Consortium; French research network on FTLD/FTLD/ALS; ITALSGEN Consortium; Hernandez DG, Arepalli S, Sabatelli M, Mora G, Corbo M, Giannini F, Calvo A, Englund E, Borghero G, Floris GL, Remes AM, Laaksovirta H, McCluskey L, Trojanowski JQ, Van Deerlin VM, Schellenberg GD, Nalls MA, Drory VE, Lu CS, Yeh TH, Ishiura H, Takahashi Y, Tsuji S, Le Ber I, Brice A, Drepper C, Williams N, Kirby J, Shaw P, Hardy J, Tienari PJ, Heutink P, Morris HR, Pickering-Brown S, Traynor BJ. Majounie E, et al. Among authors: renton ae. Lancet Neurol. 2012 Apr;11(4):323-30. doi: 10.1016/S1474-4422(12)70043-1. Epub 2012 Mar 9. Lancet Neurol. 2012. PMID: 22406228 Free PMC article.
Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion.
Englund E, Gustafson L, Passant U, Majounie E, Renton AE, Traynor BJ, Rohrer JD, Mok K, Hardy J. Englund E, et al. Among authors: renton ae. Neurobiol Aging. 2012 Aug;33(8):1850.e13-6. doi: 10.1016/j.neurobiolaging.2012.02.019. Epub 2012 Apr 6. Neurobiol Aging. 2012. PMID: 22483864 Free PMC article.
Large C9orf72 repeat expansions are not a common cause of Parkinson's disease.
Majounie E, Abramzon Y, Renton AE, Keller MF, Traynor BJ, Singleton AB. Majounie E, et al. Among authors: renton ae. Neurobiol Aging. 2012 Oct;33(10):2527.e1-2. doi: 10.1016/j.neurobiolaging.2012.05.007. Epub 2012 Jun 20. Neurobiol Aging. 2012. PMID: 22721568 Free PMC article.
CRESTing the ALS mountain.
Renton AE, Traynor BJ. Renton AE, et al. Nat Neurosci. 2013 Jul;16(7):774-5. doi: 10.1038/nn.3444. Nat Neurosci. 2013. PMID: 23799466 Free PMC article. No abstract available.
Clinical Characteristics of C9ORF72-Linked Frontotemporal Lobar Degeneration.
Kaivorinne AL, Bode MK, Paavola L, Tuominen H, Kallio M, Renton AE, Traynor BJ, Moilanen V, Remes AM. Kaivorinne AL, et al. Among authors: renton ae. Dement Geriatr Cogn Dis Extra. 2013 Aug 20;3(1):251-62. doi: 10.1159/000351859. eCollection 2013. Dement Geriatr Cogn Dis Extra. 2013. PMID: 24052799 Free PMC article.
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis.
Johnson JO, Pioro EP, Boehringer A, Chia R, Feit H, Renton AE, Pliner HA, Abramzon Y, Marangi G, Winborn BJ, Gibbs JR, Nalls MA, Morgan S, Shoai M, Hardy J, Pittman A, Orrell RW, Malaspina A, Sidle KC, Fratta P, Harms MB, Baloh RH, Pestronk A, Weihl CC, Rogaeva E, Zinman L, Drory VE, Borghero G, Mora G, Calvo A, Rothstein JD; ITALSGEN; Drepper C, Sendtner M, Singleton AB, Taylor JP, Cookson MR, Restagno G, Sabatelli M, Bowser R, Chiò A, Traynor BJ. Johnson JO, et al. Among authors: renton ae. Nat Neurosci. 2014 May;17(5):664-666. doi: 10.1038/nn.3688. Epub 2014 Mar 30. Nat Neurosci. 2014. PMID: 24686783 Free PMC article.
95 results