Perrine Charles

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

Markus Wolff, Katrine M. Johannesen, Ulrike B. S. Hedrich et al. · Brain · 2017 · 575 citations · Full text

Medicine, Genetics, Neurology +17

Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum

Giovanni Stévanin, Filippo M. Santorelli, Hamid Azzedine et al. · Nature Genetics · 2007 · 332 citations

Medicine, Neurology, Neuroscience +8

Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study

Heike Jacobi, Sophie Tézenas du Montcel, Peter Bauer et al. · The Lancet Neurology · 2015 · 299 citations

Medicine, Neurology, Neuroscience +16

Negative regulation of central nervous system myelination by polysialylated-neural cell adhesion molecule

Perrine Charles, M. P. Hernandez, Bruno Stankoff et al. · Proceedings of the National Academy of Sciences · 2000 · 293 citations

Life Sciences, Neurobiology, Neuroscience +15

Neurofascin Is a Glial Receptor for the Paranodin/Caspr-Contactin Axonal Complex at the Axoglial Junction

Perrine Charles, Steven Tait, Catherine Faivre‐Sarrailh et al. · Current Biology · 2002 · 288 citations · Full text

Medicine, Neurobiology, Neuroscience +14