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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: couratier p. Neurology. 2009 May 12;72(19):1669-76. doi: 10.1212/WNL.0b013e3181a55f1c. Neurology. 2009. PMID: 19433740
Motor neuron disease after electric injury.
Jafari H, Couratier P, Camu W. Jafari H, et al. Among authors: couratier p. J Neurol Neurosurg Psychiatry. 2001 Aug;71(2):265-7. doi: 10.1136/jnnp.71.2.265. J Neurol Neurosurg Psychiatry. 2001. PMID: 11459909 Free PMC article.
Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutations.
Corcia P, Valdmanis P, Millecamps S, Lionnet C, Blasco H, Mouzat K, Daoud H, Belzil V, Morales R, Pageot N, Danel-Brunaud V, Vandenberghe N, Pradat PF, Couratier P, Salachas F, Lumbroso S, Rouleau GA, Meininger V, Camu W. Corcia P, et al. Among authors: couratier p. Neurology. 2012 May 8;78(19):1519-26. doi: 10.1212/WNL.0b013e3182553c88. Epub 2012 Apr 25. Neurology. 2012. PMID: 22539580
SOD1 mutation can mask C9orf72 abnormal expansion.
Corcia P, Blasco H, Besson G, Camdessanché JP, Pautot V, Beltran S, Couratier P, Andres C, Camu W, Vourc'h P. Corcia P, et al. Among authors: couratier p. Eur J Neurol. 2017 Apr;24(4):e24. doi: 10.1111/ene.13257. Eur J Neurol. 2017. PMID: 28322003 No abstract available.
Causes of death amongst French patients with amyotrophic lateral sclerosis: a prospective study.
Gil J, Funalot B, Verschueren A, Danel-Brunaud V, Camu W, Vandenberghe N, Desnuelle C, Guy N, Camdessanche JP, Cintas P, Carluer L, Pittion S, Nicolas G, Corcia P, Fleury MC, Maugras C, Besson G, Le Masson G, Couratier P. Gil J, et al. Among authors: couratier p. Eur J Neurol. 2008 Nov;15(11):1245-51. doi: 10.1111/j.1468-1331.2008.02307.x. Eur J Neurol. 2008. PMID: 18973614
Genetics of amyotrophic lateral sclerosis.
Corcia P, Couratier P, Blasco H, Andres CR, Beltran S, Meininger V, Vourc'h P. Corcia P, et al. Among authors: couratier p. Rev Neurol (Paris). 2017 May;173(5):254-262. doi: 10.1016/j.neurol.2017.03.030. Epub 2017 Apr 25. Rev Neurol (Paris). 2017. PMID: 28449881 Review.
A new MRI rating scale for progressive supranuclear palsy and multiple system atrophy: validity and reliability.
Rolland Y, Vérin M, Payan CA, Duchesne S, Kraft E, Hauser TK, Jarosz J, Deasy N, Defevbre L, Delmaire C, Dormont D, Ludolph AC, Bensimon G, Leigh PN; NNIPPS Study Group. Rolland Y, et al. J Neurol Neurosurg Psychiatry. 2011 Sep;82(9):1025-32. doi: 10.1136/jnnp.2010.214890. Epub 2011 Mar 8. J Neurol Neurosurg Psychiatry. 2011. PMID: 21386111 Free PMC article.
279 results