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Page 1
[Internet and amyotrophic lateral sclerosis treatment: what is wrong?].
Meininger V, Antoine JC, Arne-Bes MC, Broussolle E, Bruneteau G, Camdessanche JP, Camu W, Carluer L, Cintas P, Clavelou P, Corcia P, Couratier P, Danel-Brunaud V, Desnuelle C, Destée A, Dib M, Fleury MC, Furby A, Giroud M, Gonzales J, Guy N, Kolev I, Lacomblez L, Lardillier-Noel D, Le Forestier N, Maugin D, Nicolas G, Pittion S, Pouget J, Pradat PF, Rousso E, Salachas F, Soriani MH, Tranchant C, Vandenberghe N, Verschueren A, Viader F, Vial C. Meininger V, et al. Rev Neurol (Paris). 2009 Mar;165(3):207-10. doi: 10.1016/j.neurol.2009.01.003. Epub 2009 Feb 12. Rev Neurol (Paris). 2009. PMID: 19217130 French. No abstract available.
[Update on fundamental and clinical research in amyotrophic lateral sclerosis].
Pradat PF, Camdessanché JP, Carluer L, Cintas P, Corcia P, Danel-Brunaud V, Echaniz-Laguna A, Gonzalez J, Nicolas G, Vandenberghe N, Verschueren A; coordination des centres de prise en charge des patients atteints de SLA. Pradat PF, et al. Rev Neurol (Paris). 2009 Jun-Jul;165(6-7):532-41. doi: 10.1016/j.neurol.2009.01.038. Epub 2009 May 5. Rev Neurol (Paris). 2009. PMID: 19419744 Review. French.
Questioning on the role of D amino acid oxidase in familial amyotrophic lateral sclerosis.
Millecamps S, Da Barroca S, Cazeneuve C, Salachas F, Pradat PF, Danel-Brunaud V, Vandenberghe N, Lacomblez L, Le Forestier N, Bruneteau G, Camu W, Brice A, Meininger V, LeGuern E. Millecamps S, et al. Proc Natl Acad Sci U S A. 2010 Jun 29;107(26):E107; author reply E108. doi: 10.1073/pnas.1006190107. Epub 2010 Jun 10. Proc Natl Acad Sci U S A. 2010. PMID: 20538972 Free PMC article. No abstract available.
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. 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.
Screening of OPTN in French familial amyotrophic lateral sclerosis.
Millecamps S, Boillée S, Chabrol E, Camu W, Cazeneuve C, Salachas F, Pradat PF, Danel-Brunaud V, Vandenberghe N, Corcia P, Le Forestier N, Lacomblez L, Bruneteau G, Seilhean D, Brice A, Feingold J, Meininger V, LeGuern E. Millecamps S, et al. Neurobiol Aging. 2011 Mar;32(3):557.e11-3. doi: 10.1016/j.neurobiolaging.2010.11.005. Epub 2011 Jan 8. Neurobiol Aging. 2011. PMID: 21220178
Mutations in UBQLN2 are rare in French amyotrophic lateral sclerosis.
Millecamps S, Corcia P, Cazeneuve C, Boillée S, Seilhean D, Danel-Brunaud V, Vandenberghe N, Pradat PF, Le Forestier N, Lacomblez L, Bruneteau G, Camu W, Brice A, Meininger V, LeGuern E, Salachas F. Millecamps S, et al. Neurobiol Aging. 2012 Apr;33(4):839.e1-3. doi: 10.1016/j.neurobiolaging.2011.11.010. Epub 2011 Dec 9. Neurobiol Aging. 2012. PMID: 22169395
32 results