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[Internet and amyotrophic lateral sclerosis treatment: what is wrong?].
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.
[A clinical, neurophysiological and molecular study of 12 patients from 4 families with spinal and bulbar muscular atrophy].
Echaniz-Laguna A, Rousso E, Anheim M, Fleury M, Cossée M, Tranchant C.
Echaniz-Laguna A, et al. Among authors: rousso e.
Rev Neurol (Paris). 2005 Apr;161(4):437-44. doi: 10.1016/s0035-3787(05)85073-8.
Rev Neurol (Paris). 2005.
PMID: 15924079
French.
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A family with early-onset and rapidly progressive X-linked spinal and bulbar muscular atrophy.
Echaniz-Laguna A, Rousso E, Anheim M, Cossée M, Tranchant C.
Echaniz-Laguna A, et al. Among authors: rousso e.
Neurology. 2005 Apr 26;64(8):1458-60. doi: 10.1212/01.WNL.0000158617.41819.F3.
Neurology. 2005.
PMID: 15851746
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Study of the HFE gene common polymorphisms in French patients with sporadic amyotrophic lateral sclerosis.
Praline J, Blasco H, Vourc'h P, Rat V, Gendrot C, Camu W, Andres CR; French ALS Study Group.
Praline J, et al.
J Neurol Sci. 2012 Jun 15;317(1-2):58-61. doi: 10.1016/j.jns.2012.02.029. Epub 2012 Mar 14.
J Neurol Sci. 2012.
PMID: 22425014
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[Recurrent facial palsy, primary Gougerot-Sjögren's syndrome and vitamin B12 deficiency].
Rousso E, Noel E, Brogard JM, Blicklé JF, Andrès E.
Rousso E, et al.
Presse Med. 2005 Jan 29;34(2 Pt 1):107-8. doi: 10.1016/s0755-4982(05)88238-7.
Presse Med. 2005.
PMID: 15687979
French.
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