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Primary progressive aphasias associated with C9orf72 expansions: Another side of the story.
Saracino D, Géraudie A, Remes AM, Ferrieux S, Noguès-Lassiaille M, Bottani S, Cipriano L, Houot M, Funkiewiez A, Camuzat A, Rinaldi D, Teichmann M, Pariente J, Couratier P, Boutoleau-Bretonnière C, Auriacombe S, Etcharry-Bouyx F, Levy R, Migliaccio R, Solje E, Le Ber I; French research network on FTD/FTD-ALS and PREV-DEMALS study groups. Saracino D, et al. Among authors: levy r. Cortex. 2021 Dec;145:145-159. doi: 10.1016/j.cortex.2021.09.005. Epub 2021 Oct 1. Cortex. 2021. PMID: 34717271
Visualization of disconnection syndromes in humans.
Thiebaut de Schotten M, Kinkingnéhun S, Delmaire C, Lehéricy S, Duffau H, Thivard L, Volle E, Levy R, Dubois B, Bartolomeo P. Thiebaut de Schotten M, et al. Among authors: levy r. Cortex. 2008 Sep;44(8):1097-103. doi: 10.1016/j.cortex.2008.02.003. Epub 2008 May 23. Cortex. 2008. PMID: 18602092
[Semantic dementia associated with amyotrophic lateral sclerosis].
de Souza LC, Sarazin M, Samri D, Kas A, Léhericy S, Lévy R, Dubois B. de Souza LC, et al. Among authors: levy r. Rev Neurol (Paris). 2009 Mar;165(3):278-81. doi: 10.1016/j.neurol.2008.06.008. Epub 2008 Aug 28. Rev Neurol (Paris). 2009. PMID: 18760427 French.
A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer disease.
Rovelet-Lecrux A, Legallic S, Wallon D, Flaman JM, Martinaud O, Bombois S, Rollin-Sillaire A, Michon A, Le Ber I, Pariente J, Puel M, Paquet C, Croisile B, Thomas-Antérion C, Vercelletto M, Lévy R, Frébourg T, Hannequin D, Campion D; Investigators of the GMAJ project. Rovelet-Lecrux A, et al. Among authors: levy r. Eur J Hum Genet. 2012 Jun;20(6):613-7. doi: 10.1038/ejhg.2011.225. Epub 2011 Dec 14. Eur J Hum Genet. 2012. PMID: 22166940 Free PMC article.
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. 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.
4,902 results