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European Neurology|January 1, 1996
Modelization of motor nerve conduction velocities for Charcot-Marie-Tooth (Type-1) patients. CMT-France NetworkF G Sturtz, F Chauvin, E Ollagnon-Roman, et al.
Revue Neurologique|December 24, 2022
Strategy for genetic analysis in hereditary neuropathyM Masingue, G Fernández-Eulate, R Debs, et al.
Clinical Chemistry|July 1, 1996
Molecular diagnosis of Charcot-Marie-Tooth 1A disease and hereditary neuropathy with liability to pressure palsies by quantifying CMT1A-REP sequences: consequences of recombinations at variant sites on chromosomes 17p11.2-12A Vandenberghe, P Latour, G Chauplannaz, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 23, 2008
Relapsing demyelinating disease affecting both the central and peripheral nervous systemsH Zéphir, T Stojkovic, P Latour, et al.
Journal of the American College of Cardiology|December 1, 1991
Enalapril versus digoxin in patients with congestive heart failure: a multicenter study. Canadian Enalapril Versus Digoxin Study GroupR F Davies, D S Beanlands, C Nadeau, et al.
Human Genetics|August 1, 1996
X-linked dominant Charcot-Marie-Tooth neuropathy (CMTX): new mutations in the connexin32 geneC Ressot, P Latour, F Blanquet-Grossard, et al.
Human Molecular Genetics|February 28, 1998
Fine mapping of de novo CMT1A and HNPP rearrangements within CMT1A-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombinationJ Lopes, N Ravisé, A Vandenberghe, et al.
European Journal of Neurology|February 18, 2017
Phenotypic spectrum of Charcot-Marie-Tooth disease due to LITAF/SIMPLE mutations: a study of 18 patientsR Guimarães-Costa, R Iancu Ferfoglia, S Leonard-Louis, et al.
Neurogenetics|March 25, 2000
Mutations in the X-linked form of Charcot-Marie-Tooth disease in the French populationP Latour, N Lévy, M Paret, et al.
Acta Oncologica (Stockholm, Sweden)|December 16, 2017
Antineoplastic agents exacerbating Charcot Marie Tooth disease: red flags to avoid permanent disabilityM J Ibañez-Juliá, G Berzero, G Reyes-Botero, et al.
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