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Journal of Neurology|February 17, 2015
A novel autosomal dominant leukodystrophy with specific MRI patternA Corlobé, F Taithe, P Clavelou, et al.
Neurology|February 26, 2003
Infantile ascending hereditary spastic paralysis (IAHSP): clinical features in 11 familiesG Lesca, E Eymard-Pierre, F M Santorelli, et al.
Neurology|August 27, 2003
Genetic heterogeneity of megalencephalic leukoencephalopathy and subcortical cystsC Patrono, G Di Giacinto, E Eymard-Pierre, et al.
Neurology|May 12, 2004
The effect of genotype on the natural history of eIF2B-related leukodystrophiesA Fogli, R Schiffmann, E Bertini, et al.
Molecular Genetics and Metabolism|August 15, 2017
Impact of mutations within the [Fe-S] cluster or the lipoic acid biosynthesis pathways on mitochondrial protein expression profiles in fibroblasts from patientsE Lebigot, P Gaignard, I Dorboz, et al.
Annals of Human Genetics|January 31, 2006
Golli-MBP copy number analysis by FISH, QMPSF and MAPH in 195 patients with hypomyelinating leukodystrophiesC Vaurs-Barriere, M-N Bonnet-Dupeyron, P Combes, et al.
American Journal of Human Genetics|September 22, 2001
Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlationD Rodriguez, F Gauthier, E Bertini, et al.
Revue Neurologique|October 22, 2013
[Cavitary lesions in multiple sclerosis: multicenter study on twenty patients]A Corlobé, D Renard, C Goizet, et al.
AJNR. American Journal of Neuroradiology|August 18, 2018
Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French CasesP Codjia, X Ayrignac, F Mochel, et al.
Revue Neurologique|June 17, 2011
[Natural history of adult-onset eIF2B-related disorders: a multicentric survey of 24 cases]C Carra-Dalliere, L Horzinski, X Ayrignac, et al.
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