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[SLA: a long way since Charcot].
Pradat PF, Bruneteau G, Salachas F, Meininger V. Pradat PF, et al. Among authors: bruneteau g. Rev Prat. 2003 Nov 15;53(17):1861-3. Rev Prat. 2003. PMID: 14722971 Review. French. No abstract available.
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: bruneteau g. Ann Neurol. 2007 Jul;62(1):15-20. doi: 10.1002/ana.21122. Ann Neurol. 2007. PMID: 17455292
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. Among authors: bruneteau g. Amyotroph Lateral Scler. 2008;9(1):59-62. doi: 10.1080/17482960701656940. Amyotroph Lateral Scler. 2008. PMID: 17924236
Impaired glucose tolerance in patients with amyotrophic lateral sclerosis.
Pradat PF, Bruneteau G, Gordon PH, Dupuis L, Bonnefont-Rousselot D, Simon D, Salachas F, Corcia P, Frochot V, Lacorte JM, Jardel C, Coussieu C, Le Forestier N, Lacomblez L, Loeffler JP, Meininger V. Pradat PF, et al. Among authors: bruneteau g. Amyotroph Lateral Scler. 2010;11(1-2):166-71. doi: 10.3109/17482960902822960. Amyotroph Lateral Scler. 2010. PMID: 20184518
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: bruneteau g. J Neurol. 2010 Oct;257(10):1713-7. doi: 10.1007/s00415-010-5609-1. Epub 2010 Jun 8. J Neurol. 2010. PMID: 20532545
Abnormal TDP-43 and FUS proteins in muscles of sporadic IBM: similarities in a TARDBP-linked ALS patient.
Hernandez Lain A, Millecamps S, Dubourg O, Salachas F, Bruneteau G, Lacomblez L, LeGuern E, Seilhean D, Duyckaerts C, Meininger V, Mallet J, Pradat PF. Hernandez Lain A, et al. Among authors: bruneteau g. J Neurol Neurosurg Psychiatry. 2011 Dec;82(12):1414-6. doi: 10.1136/jnnp.2010.208868. Epub 2010 Jun 18. J Neurol Neurosurg Psychiatry. 2011. PMID: 20562395 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. Among authors: bruneteau g. 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.
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