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Neurology|May 7, 2008
Severe early-onset axonal neuropathy with homozygous and compound heterozygous MFN2 mutationsG A Nicholson, C Magdelaine, D Zhu, et al.Spine|April 1, 1993
Monitoring of the motor pathway during spinal surgeryF Tabaraud, J M Boulesteix, D Moulies, et al.Journal of Neuroscience Research|June 22, 2000
Absence of P0 leads to the dysregulation of myelin gene expression and myelin morphogenesisW Xu, D Manichella, H Jiang, et al.Journal of the Neurological Sciences|April 30, 1998
Serum autoantibodies to neurofilament proteins in sporadic amyotrophic lateral sclerosisP Couratier, F H Yi, J L Preud'homme, et al.Neuroepidemiology|January 1, 1996
Survival prediction in sporadic amyotrophic lateral sclerosis. Age and clinical form at onset are independent risk factorsP M Preux, P Couratier, F Boutros-Toni, et al.Neuromuscular Disorders : NMD|October 26, 2002
Genetic heterogeneity in giant axonal neuropathy: an Algerian family not linked to chromosome 16q24.1M Tazir, J M Vallat, P Bomont, et al.European Journal of Neurology|November 27, 2019
Antibody- and macrophage-mediated segmental demyelination in chronic inflammatory demyelinating polyneuropathy: clinical, electrophysiological, immunological and pathological correlatesJ-M Vallat, S Mathis, E Vegezzi, et al.Neurology|April 23, 2003
Interferon beta-1a as an investigational treatment for CIDPJ-M Vallat, A F Hahn, J-M Léger, et al.Headache|November 1, 1993
Prevalence of headache in a representative sample of the population in a French department (Haute-Vienne-Limousin)M Munoz, M Dumas, F Boutros-Toni, et al.Revue Neurologique|January 1, 1988
[A neuro-epidemiologic survey in a Limousin town]M Munoz, M Dumas, F Boutros-Toni, et al.Pageof 18