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Page 1
TREM2 mutations are rare in a French cohort of patients with frontotemporal dementia.
Lattante S, Le Ber I, Camuzat A, Dayan S, Godard C, Van Bortel I, De Septenville A, Ciura S, Brice A, Kabashi E; French Research Network on FTD and FTD-ALS. Lattante S, et al. Among authors: brice a. Neurobiol Aging. 2013 Oct;34(10):2443.e1-2. doi: 10.1016/j.neurobiolaging.2013.04.030. Epub 2013 Jun 4. Neurobiol Aging. 2013. PMID: 23759145
Is the saitohin gene involved in neurodegenerative diseases?
Verpillat P, Ricard S, Hannequin D, Dubois B, Bou J, Camuzat A, Pradier L, Frebourg T, Brice A, Clerget-Darpoux F, Deleuze JF, Campion D; French Study Group on Alzheimer's Disease and Frontotemporal Dementia. Verpillat P, et al. Among authors: brice a. Ann Neurol. 2002 Dec;52(6):829-32. doi: 10.1002/ana.10384. Ann Neurol. 2002. PMID: 12447938
Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies.
Le Ber I, Moreira MC, Rivaud-Péchoux S, Chamayou C, Ochsner F, Kuntzer T, Tardieu M, Saïd G, Habert MO, Demarquay G, Tannier C, Beis JM, Brice A, Koenig M, Dürr A. Le Ber I, et al. Among authors: brice a. Brain. 2003 Dec;126(Pt 12):2761-72. doi: 10.1093/brain/awg283. Epub 2003 Sep 23. Brain. 2003. PMID: 14506070 Free article.
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: brice a. Brain. 2006 Nov;129(Pt 11):3051-65. doi: 10.1093/brain/awl288. Brain. 2006. PMID: 17071924
1,097 results