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A juvenile ALS-like phenotype dramatically improved after high-dose riboflavin treatment.
Carreau C, Lenglet T, Mosnier I, Lahlou G, Fargeot G, Weiss N, Demeret S, Salachas F, Veauville-Merllié A, Acquaviva C, Nadjar Y. Carreau C, et al. Among authors: salachas f. Ann Clin Transl Neurol. 2020 Feb;7(2):250-253. doi: 10.1002/acn3.50977. Epub 2020 Feb 5. Ann Clin Transl Neurol. 2020. PMID: 32022482 Free PMC article.
What has changed with riluzole?
Meininger V, Lacomblez L, Salachas F. Meininger V, et al. Among authors: salachas f. J Neurol. 2000 Dec;247:19-22. J Neurol. 2000. PMID: 11200701 Review.
APOE: a potential marker of disease progression in ALS.
Lacomblez L, Doppler V, Beucler I, Costes G, Salachas F, Raisonnier A, Le Forestier N, Pradat PF, Bruckert E, Meininger V. Lacomblez L, et al. Among authors: salachas f. Neurology. 2002 Apr 9;58(7):1112-4. doi: 10.1212/wnl.58.7.1112. Neurology. 2002. PMID: 11940705
Muscle Nogo-A expression is a prognostic marker in lower motor neuron syndromes.
Pradat PF, Bruneteau G, Gonzalez de Aguilar JL, Dupuis L, Jokic N, Salachas F, Le Forestier N, Echaniz-Laguna A, Dubourg O, Hauw JJ, Tranchant C, Loeffler JP, Meininger V. Pradat PF, et al. Among authors: salachas f. Ann Neurol. 2007 Jul;62(1):15-20. doi: 10.1002/ana.21122. Ann Neurol. 2007. PMID: 17455292
Progression in ALS is not linear but is curvilinear.
Gordon PH, Cheng B, Salachas F, Pradat PF, Bruneteau G, Corcia P, Lacomblez L, Meininger V. Gordon PH, et al. Among authors: salachas f. J Neurol. 2010 Oct;257(10):1713-7. doi: 10.1007/s00415-010-5609-1. Epub 2010 Jun 8. J Neurol. 2010. PMID: 20532545
Safety of home parenteral nutrition in patients with amyotrophic lateral sclerosis: a French national survey.
Abdelnour-Mallet M, Verschueren A, Guy N, Soriani MH, Chalbi M, Gordon P, Salachas F, Bruneteau G, le Forestier N, Lenglet T, Desnuelle C, Clavelou P, Pouget J, Meininger V, Pradat PF. Abdelnour-Mallet M, et al. Among authors: salachas f. Amyotroph Lateral Scler. 2011 May;12(3):178-84. doi: 10.3109/17482968.2010.531741. Epub 2010 Nov 15. Amyotroph Lateral Scler. 2011. PMID: 21073397
Abnormalities of satellite cells function in amyotrophic lateral sclerosis.
Pradat PF, Barani A, Wanschitz J, Dubourg O, Lombès A, Bigot A, Mouly V, Bruneteau G, Salachas F, Lenglet T, Meininger V, Butler-Browne G. Pradat PF, et al. Among authors: salachas f. Amyotroph Lateral Scler. 2011 Jul;12(4):264-71. doi: 10.3109/17482968.2011.566618. Epub 2011 Apr 8. Amyotroph Lateral Scler. 2011. PMID: 21473708
Muscle gene expression is a marker of amyotrophic lateral sclerosis severity.
Pradat PF, Dubourg O, de Tapia M, di Scala F, Dupuis L, Lenglet T, Bruneteau G, Salachas F, Lacomblez L, Corvol JC, Demougin P, Primig M, Meininger V, Loeffler JP, Gonzalez de Aguilar JL. Pradat PF, et al. Among authors: salachas f. Neurodegener Dis. 2012;9(1):38-52. doi: 10.1159/000329723. Epub 2011 Sep 21. Neurodegener Dis. 2012. PMID: 21934272
Improving survival in a large French ALS center cohort.
Gordon PH, Salachas F, Bruneteau G, Pradat PF, Lacomblez L, Gonzalez-Bermejo J, Morelot-Panzini C, Similowski T, Elbaz A, Meininger V. Gordon PH, et al. Among authors: salachas f. J Neurol. 2012 Sep;259(9):1788-92. doi: 10.1007/s00415-011-6403-4. Epub 2012 Jan 19. J Neurol. 2012. PMID: 22258480
184 results