Publications du centre de référence

Le Ber I, Sarazin M. Génétique des DLFT. La Lettre du Neurologue, Novembre 2009.

Le Ber I, Camuzat A, Berger E, Hannequin D, Laquerrière A, Golfier V, Seilhan D, Viennet G, Couratier P, Verpillat P, Heath S, Camu W, Martinaud O, Lacomblez L, Vercelletto M, Salachas F, Sellal F, Didic M, Thomas-Anterion C, Puel M, Michel BF, Besse C, Duyckaerts C, Meininger V, Campion D, Dubois B, Brice A and the French research network on FTD/FTD-MND. Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease. Neurology 2009 ; 72:1669–1676

Benajiba L, Le Ber I, Camuzat A, Lacoste M, Thomas-Anterion C, Couratier P, Legallic S, Salachas F, Hannequin D, Decousus M, Lacomblez L, Guedj E, Golfier, V, Camu, W, Dubois B, Campion D, Meininger V, Brice A and the French clinical and genetic research network on FTD/FTD-MND. TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration. Ann Neurol 2009 ;65:470-473

Rovelet-Lecrux A, Lecourtois M, Thomas-Anterion C, Le Ber I, Brice A, Frebourg T, Hannequin D, Campion D. Partial deletion of the MAPT gene : a novel mechanism of FTDP-17. Hum Mutat. 2009.

Guedj E, Allali G, Goetz C, Le Ber I, Volteau M, Lacomblez L, Véra P, Hitzel A, Hannequin D, Decousus M, Thomas-Antérion C, Magne C, Vercelletto M, Bernard AM, Didic M, Lotterie JA, Puel M, Brice A, The French research network on FTD/FTD-MND, Habert MO, Dubois B. Frontal Assessment Battery is a marker of dorsolateral and medial frontal functions : a SPECT study in frontotemporal dementia. J Neurol Sci. 2008 Oct 15 ;273(1-2):84-7.

Rovelet-Lecrux A, Deramecorut V, Legallic S, Maurage CA, Le Ber I, Brice A, Lambert JC, Frébourg T, Hannequin D , Pasquier F, Campion D. Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease. Neurobiol Dis. 2008 Apr 7. [Epub ahead of print]

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, 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 and the French research network on FTD/FTD-MND**. Phenotype variability in progranulin mutation carriers : a clinical, neuropsychological, imaging and genetic study. Brain 2008 131 : 732-746.

Le Ber I, Dubois B. Les démences frontotemporales. Presse Med, 2007 ;36:1477-1484.

Guedj E, Le Ber I, Lacomblez L, Dubois B, Verpillat P, Didic M, Salachas F, Véra P, Hannequin D, Lotterie JA, Puel M, Decousus M, Thomas-Antérion C, Magne C, Vercelletto M, Bernard AM, Golfier V, Pasquier J, Michel BF, Namer I, Sellal F, Bochet J, Volteau M, Brice A, Meininger V, The French research network on FTD/FTD-MND, Habert MO. Brain SPECT perfusion of frontotemporal dementia associated with motor neuron disease. Neurology, 2007 ; 69(5):488-90.

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, and the French Research Network on FTD/FTD-MND. Progranulin null mutations in both sporadic and familial frontotemporal dementia. Human Mutation, 2007 Sep ;28(9):846-55

van der Zee J, Le Ber I, Maurer-Stroh S, Engelborghs S, Gijselinck I, Camuzat A, Brouwers N, Vandenberghe R, Sleegers K, Hannequin D, Dermaut B, Schymkowitz J, Campion D, Santens P, Martin JJ, Lacomblez L, De Pooter T, Peeters K, Mattheijssens M, Vercelletto M, Van den Broeck M, Cruts M, De Deyn P, Rousseau F, Brice A, Van Broeckhoven C. Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia. Hum Mutat. 2007 ;7 ;28(4):416.

Baba Y, Baker MC, Le Ber I, Brice A, Maeck L, Kohlhase J, Yasuda M, Stoppe G, Bugiani O, Sperfeld AD, Tsuboi Y, Uitti RJ, Farrer MJ, Ghetti B, Hutton ML, Wszolek ZK. Clinical and Genetic Features of Families With Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17 With a P301S tau Mutation. Journal of Neural Transmission, 2007

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, the French research network on FTD/FTD-MND, Brice A, Habert MO, Dubois B. Demographic, neurological, behavioural characteristics and brain perfusion SPECT in frontal variant of frontotemporal dementia. Brain. 2006 Nov ;129:3051-3065.