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Revue Neurologique|September 16, 1999
[Acute demyelinating motor neuropathy: an atypical form of the Guillain-Barre syndrome?]P Corcia, A Beaume, A M Guennoc, et al.Expert Review of Molecular Diagnostics|June 9, 2016
Further development of biomarkers in amyotrophic lateral sclerosisH Blasco, P Vourc'h, P F Pradat, et al.Revue Neurologique|June 17, 2008
[Progressive anarthria: an individual entity]N Limousin, S Rimbaux, K Mondon, et al.Revue Neurologique|August 12, 2003
[Glycogenesis due to adult phosphorylase kinase deficiency]P Couratier, L Magy, C Baussan, et al.Revue Neurologique|October 17, 1998
[Lead intoxication and amyotrophic lateral sclerosis]P Couratier, P Bernet-Bernady, T Truong, et al.Neurophysiologie Clinique = Clinical Neurophysiology|January 29, 2002
Sleep and brain lesions: a critical review of the literature and additional new casesA Autret, B Lucas, K Mondon, et al.Acta Neurologica Scandinavica|March 2, 2011
Predictive value of motor evoked potentials in clinically isolated syndromeM Pallix-Guyot, A-M Guennoc, H Blasco, et al.Revue Neurologique|February 5, 1999
[Significance of single photon emission computed tomography and akinetic mutism]E Hazouard, A Legras, P Corcia, et al.The American Journal of Clinical Nutrition|August 28, 2001
Factors correlated with hypermetabolism in patients with amyotrophic lateral sclerosisJ C Desport, P M Preux, L Magy, et al.European Journal of Neurology|January 16, 2007
Bilateral hand amyotrophy with PMP-22 gene deletionA Gochard, A M Guennoc, J Praline, et al.Pageof 15