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SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations.
Millecamps S, Salachas F, Cazeneuve C, Gordon P, Bricka B, Camuzat A, Guillot-Noël L, Russaouen O, Bruneteau G, Pradat PF, Le Forestier N, Vandenberghe N, Danel-Brunaud V, Guy N, Thauvin-Robinet C, Lacomblez L, Couratier P, Hannequin D, Seilhean D, Le Ber I, Corcia P, Camu W, Brice A, Rouleau G, LeGuern E, Meininger V. Millecamps S, et al. Among authors: corcia p. J Med Genet. 2010 Aug;47(8):554-60. doi: 10.1136/jmg.2010.077180. Epub 2010 Jun 24. J Med Genet. 2010. PMID: 20577002 Free article.
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.
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
Dyslipidemia is a protective factor in amyotrophic lateral sclerosis.
Dupuis L, Corcia P, Fergani A, Gonzalez De Aguilar JL, Bonnefont-Rousselot D, Bittar R, Seilhean D, Hauw JJ, Lacomblez L, Loeffler JP, Meininger V. Dupuis L, et al. Among authors: corcia p. Neurology. 2008 Mar 25;70(13):1004-9. doi: 10.1212/01.wnl.0000285080.70324.27. Epub 2008 Jan 16. Neurology. 2008. PMID: 18199832
Management of amyotrophic lateral sclerosis.
Corcia P, Meininger V. Corcia P, et al. Drugs. 2008;68(8):1037-48. doi: 10.2165/00003495-200868080-00003. Drugs. 2008. PMID: 18484797 Review.
336 results