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Pure cerebellar ataxia linked to large C9orf72 repeat expansion.
Corcia P, Vourc'h P, Guennoc AM, Del Mar Amador M, Blasco H, Andres C, Couratier P, Gordon PH, Meininger V. Corcia P, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2016;17(3-4):301-3. doi: 10.3109/21678421.2015.1113298. Epub 2015 Nov 26. Amyotroph Lateral Scler Frontotemporal Degener. 2016. PMID: 26609732 No abstract available.
SMN1 gene, but not SMN2, is a risk factor for sporadic ALS.
Corcia P, Camu W, Halimi JM, Vourc'h P, Antar C, Vedrine S, Giraudeau B, de Toffol B, Andres CR; French ALS Study Group. Corcia P, et al. Neurology. 2006 Oct 10;67(7):1147-50. doi: 10.1212/01.wnl.0000233830.85206.1e. Epub 2006 Aug 23. Neurology. 2006. PMID: 16931506 Clinical Trial.
Bilateral hand amyotrophy with PMP-22 gene deletion.
Gochard A, Guennoc AM, Praline J, Malinge MC, de Toffol B, Corcia P. Gochard A, et al. Among authors: corcia p. Eur J Neurol. 2007 Jan;14(1):115-6. doi: 10.1111/j.1468-1331.2006.01576.x. Eur J Neurol. 2007. PMID: 17222125
ALS and mercury intoxication: a relationship?
Praline J, Guennoc AM, Limousin N, Hallak H, de Toffol B, Corcia P. Praline J, et al. Among authors: corcia p. Clin Neurol Neurosurg. 2007 Dec;109(10):880-3. doi: 10.1016/j.clineuro.2007.07.008. Epub 2007 Aug 23. Clin Neurol Neurosurg. 2007. PMID: 17719172
336 results