Corcia P - Search Results

1

Association between divalent metal transport 1 encoding gene (SLC11A2) and disease duration in amyotrophic lateral sclerosis.

Blasco H, Vourc'h P, Nadjar Y, Ribourtout B, Gordon PH, Guettard YO, Camu W, Praline J, Meininger V, Andres CR, Corcia P; French ALS study group. Blasco H, et al. Among authors: corcia p. J Neurol Sci. 2011 Apr 15;303(1-2):124-7. doi: 10.1016/j.jns.2010.12.018. Epub 2011 Jan 26. J Neurol Sci. 2011. PMID: 21276595

2

Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis.

Corcia P, Mayeux-Portas V, Khoris J, de Toffol B, Autret A, Müh JP, Camu W, Andres C; French ALS Research Group. Amyotrophic Lateral Sclerosis. Corcia P, et al. Ann Neurol. 2002 Feb;51(2):243-6. doi: 10.1002/ana.10104. Ann Neurol. 2002. PMID: 11835381

3

SMN1 gene study in three families in which ALS and spinal muscular atrophy co-exist.

Corcia P, Khoris J, Couratier P, Mayeux-Portas V, Bieth E, De Toffol B, Autret A, Müh JP, Andres C, Camu W. Corcia P, et al. Neurology. 2002 Nov 12;59(9):1464-6. doi: 10.1212/01.wnl.0000032500.73621.c5. Neurology. 2002. PMID: 12427909

4

[Acute motor axonal neuropathy, enterovirus and Amyotrophic lateral sclerosis: can there be a link?].

Corcia P, Giraud P, Guennoc AM, de Toffol B, Autret A. Corcia P, et al. Rev Neurol (Paris). 2003 Jan;159(1):80-2. Rev Neurol (Paris). 2003. PMID: 12618659 French.

5

A clustering of conjugal amyotrophic lateral sclerosis in southeastern France.

Corcia P, Jafari-Schluep HF, Lardillier D, Mazyad H, Giraud P, Clavelou P, Pouget J, Camu W. Corcia P, et al. Arch Neurol. 2003 Apr;60(4):553-7. doi: 10.1001/archneur.60.4.553. Arch Neurol. 2003. PMID: 12707069

6

N19S, a new SOD1 mutation in sporadic amyotrophic lateral sclerosis: no evidence for disease causation.

Mayeux V, Corcia P, Besson G, Jafari-Schluep HF, Briolotti V, Camu W. Mayeux V, et al. Among authors: corcia p. Ann Neurol. 2003 Jun;53(6):815-8. doi: 10.1002/ana.10605. Ann Neurol. 2003. PMID: 12783432

7

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.

8

[Methods of the announcement of amyotrophic lateral sclerosis diagnosis in familial forms].

Corcia P. Corcia P. Rev Neurol (Paris). 2006 Jun;162 Spec No 2:4S122-4S126. Rev Neurol (Paris). 2006. PMID: 17128099 French.

9

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

10

Emergent EEG in clinical practice.

Praline J, Grujic J, Corcia P, Lucas B, Hommet C, Autret A, de Toffol B. Praline J, et al. Among authors: corcia p. Clin Neurophysiol. 2007 Oct;118(10):2149-55. doi: 10.1016/j.clinph.2007.07.003. Epub 2007 Aug 20. Clin Neurophysiol. 2007. PMID: 17709288

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