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Page 1
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: camuzat a. Cortex. 2021 Dec;145:145-159. doi: 10.1016/j.cortex.2021.09.005. Epub 2021 Oct 1. Cortex. 2021. PMID: 34717271
Association between the extended tau haplotype and frontotemporal dementia.
Verpillat P, Camuzat A, Hannequin D, Thomas-Anterion C, Puel M, Belliard S, Dubois B, Didic M, Michel BF, Lacomblez L, Moreaud O, Sellal F, Golfier V, Campion D, Clerget-Darpoux F, Brice A. Verpillat P, et al. Among authors: camuzat a. Arch Neurol. 2002 Jun;59(6):935-9. doi: 10.1001/archneur.59.6.935. Arch Neurol. 2002. PMID: 12056929
Apolipoprotein E gene in frontotemporal dementia: an association study and meta-analysis.
Verpillat P, Camuzat A, Hannequin D, Thomas-Anterion C, Puel M, Belliard S, Dubois B, Didic M, Lacomblez L, Moreaud O, Golfier V, Campion D, Brice A, Clerget-Darpoux F. Verpillat P, et al. Among authors: camuzat a. Eur J Hum Genet. 2002 Jul;10(7):399-405. doi: 10.1038/sj.ejhg.5200820. Eur J Hum Genet. 2002. PMID: 12107813
Demographic, neurological and behavioural characteristics and brain perfusion SPECT in frontal variant of frontotemporal dementia.
Le Ber I, Guedj E, Gabelle A, Verpillat P, Volteau M, Thomas-Anterion C, Decousus M, Hannequin D, Véra P, Lacomblez L, Camuzat A, Didic M, Puel M, Lotterie JA, Golfier V, Bernard AM, Vercelletto M, Magne C, Sellal F, Namer I, Michel BF, Pasquier J, Salachas F, Bochet J; French research network on FTD/FTD-MND; Brice A, Habert MO, Dubois B. Le Ber I, et al. Among authors: camuzat a. Brain. 2006 Nov;129(Pt 11):3051-65. doi: 10.1093/brain/awl288. Brain. 2006. PMID: 17071924
Progranulin null mutations in both sporadic and familial frontotemporal dementia.
Le Ber I, van der Zee J, Hannequin D, Gijselinck I, Campion D, Puel M, Laquerrière A, De Pooter T, Camuzat A, Van den Broeck M, Dubois B, Sellal F, Lacomblez L, Vercelletto M, Thomas-Antérion C, Michel BF, Golfier V, Didic M, Salachas F, Duyckaerts C, Cruts M, Verpillat P, Van Broeckhoven C, Brice A; French Research Network on FTD/FTD-MND. Le Ber I, et al. Among authors: camuzat a. Hum Mutat. 2007 Sep;28(9):846-55. doi: 10.1002/humu.20520. Hum Mutat. 2007. PMID: 17436289
Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?
Charles P, Camuzat A, Benammar N, Sellal F, Destée A, Bonnet AM, Lesage S, Le Ber I, Stevanin G, Dürr A, Brice A; French Parkinson's Disease Genetic Study Group. Charles P, et al. Among authors: camuzat a. Neurology. 2007 Nov 20;69(21):1970-5. doi: 10.1212/01.wnl.0000269323.21969.db. Epub 2007 Jun 13. Neurology. 2007. PMID: 17568014
Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study.
Le Ber I, Camuzat A, Hannequin D, Pasquier F, Guedj E, Rovelet-Lecrux A, Hahn-Barma V, van der Zee J, Clot F, Bakchine S, Puel M, Ghanim M, Lacomblez L, Mikol J, Deramecourt V, Lejeune P, de la Sayette V, Belliard S, Vercelletto M, Meyrignac C, Van Broeckhoven C, Lambert JC, Verpillat P, Campion D, Habert MO, Dubois B, Brice A; French research network on FTD/FTD-MND. Le Ber I, et al. Among authors: camuzat a. Brain. 2008 Mar;131(Pt 3):732-46. doi: 10.1093/brain/awn012. Epub 2008 Feb 1. Brain. 2008. PMID: 18245784
125 results