Corcia P - Search Results

1

Metabolomics in cerebrospinal fluid of patients with amyotrophic lateral sclerosis: an untargeted approach via high-resolution mass spectrometry.

Blasco H, Corcia P, Pradat PF, Bocca C, Gordon PH, Veyrat-Durebex C, Mavel S, Nadal-Desbarats L, Moreau C, Devos D, Andres CR, Emond P. Blasco H, et al. Among authors: corcia p. J Proteome Res. 2013 Aug 2;12(8):3746-54. doi: 10.1021/pr400376e. Epub 2013 Jul 16. J Proteome Res. 2013. PMID: 23859630

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

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

5

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.

6

[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.

7

Causes of death in a post-mortem series of ALS patients.

Corcia P, Pradat PF, Salachas F, Bruneteau G, Forestier Nl, Seilhean D, Hauw JJ, Meininger V. Corcia P, et al. Amyotroph Lateral Scler. 2008;9(1):59-62. doi: 10.1080/17482960701656940. Amyotroph Lateral Scler. 2008. PMID: 17924236

8

[Genetics of motor neuron disorders].

Corcia P, Praline J, Vourc'h P, Andres C. Corcia P, et al. Rev Neurol (Paris). 2008 Feb;164(2):115-30. doi: 10.1016/j.neurol.2007.10.002. Epub 2008 Feb 20. Rev Neurol (Paris). 2008. PMID: 18358870 Review. French.

9

Mutations of the ANG gene in French patients with sporadic amyotrophic lateral sclerosis.

Paubel A, Violette J, Amy M, Praline J, Meininger V, Camu W, Corcia P, Andres CR, Vourc'h P; French Amyotrophic Lateral Sclerosis (ALS) Study Group. Paubel A, et al. Among authors: corcia p. Arch Neurol. 2008 Oct;65(10):1333-6. doi: 10.1001/archneur.65.10.1333. Arch Neurol. 2008. PMID: 18852347

10

CADASIL and ALS: a link?

Praline J, Limousin N, Vourc'h P, Pallix M, Debiais S, Guennoc AM, Andres CR, Corcia P. Praline J, et al. Among authors: corcia p. Amyotroph Lateral Scler. 2010 Aug;11(4):399-401. doi: 10.1080/17482960903033153. Amyotroph Lateral Scler. 2010. PMID: 19488902

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