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Page 1
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease.
Le Ber I, Camuzat A, Berger E, Hannequin D, Laquerrière A, Golfier V, Seilhean 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; French Research Network on FTD/FTD-MND. Le Ber I, et al. Among authors: martinaud o. Neurology. 2009 May 12;72(19):1669-76. doi: 10.1212/WNL.0b013e3181a55f1c. Neurology. 2009. PMID: 19433740
[Confusional state and agitation].
Martinaud O, Hannequin D. Martinaud O, et al. Rev Prat. 2000 Nov 15;50(18):1994-8. Rev Prat. 2000. PMID: 11192967 Review. French.
[Two confusion scales].
Martinaud O, Hannequin D. Martinaud O, et al. Rev Neurol (Paris). 2001 Jul;157(6-7):708-12. Rev Neurol (Paris). 2001. PMID: 11458193 French. No abstract available.
Hemidystonia as initial manifestation of sporadic Creutzfeldt-Jakob disease.
Maltête D, Guyant-Maréchal L, Gérardin E, Laquerrière A, Martinaud O, Mihout B, Hannequin D. Maltête D, et al. Among authors: martinaud o. Eur J Neurol. 2006 Jun;13(6):667-8. doi: 10.1111/j.1468-1331.2006.01246.x. Eur J Neurol. 2006. PMID: 16796596 No abstract available.
[Argyrophilic grain disease: synergistic component of dementia?].
Wallon D, Sommervogel C, Laquerrière A, Martinaud O, Lecourtois M, Hannequin D. Wallon D, et al. Among authors: martinaud o. Rev Neurol (Paris). 2010 Apr;166(4):428-32. doi: 10.1016/j.neurol.2009.10.012. Epub 2009 Dec 5. Rev Neurol (Paris). 2010. PMID: 19963233 French.
106 results