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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.
Forced collectionism after orbitofrontal damage.
Volle E, Beato R, Levy R, Dubois B. Volle E, et al. Among authors: levy r. Neurology. 2002 Feb 12;58(3):488-90. doi: 10.1212/wnl.58.3.488. Neurology. 2002. PMID: 11839860
Cognition, behavior and the frontal lobes.
Dubois B, Levy R. Dubois B, et al. Among authors: levy r. Int Psychogeriatr. 2004 Dec;16(4):379-87. doi: 10.1017/s104161020400081x. Int Psychogeriatr. 2004. PMID: 15715355 No abstract available.
Executive dysfunction and neuropsychological testing.
Dubois B, Andrade K, Levy R. Dubois B, et al. Among authors: levy r. Handb Clin Neurol. 2008;89:35-52. doi: 10.1016/S0072-9752(07)01203-1. Handb Clin Neurol. 2008. PMID: 18631729 No abstract available.
SQSTM1 mutations in French patients with frontotemporal dementia or frontotemporal dementia with amyotrophic lateral sclerosis.
Le Ber I, Camuzat A, Guerreiro R, Bouya-Ahmed K, Bras J, Nicolas G, Gabelle A, Didic M, De Septenville A, Millecamps S, Lenglet T, Latouche M, Kabashi E, Campion D, Hannequin D, Hardy J, Brice A; French Clinical and Genetic Research Network on FTD/FTD-ALS. Le Ber I, et al. JAMA Neurol. 2013 Nov;70(11):1403-10. doi: 10.1001/jamaneurol.2013.3849. JAMA Neurol. 2013. PMID: 24042580 Free PMC article.
4,902 results