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 · 558 citations · Full text

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 · 331 citations

Biology, Neuroanatomy, Genetics +8

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 · 287 citations · Full text

Paranodin/caspr-contactin Axonal Complex, Neuroanatomy, Axoglial Junction +10

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 · 286 citations

Longitudinal Cohort Study, Neurological Disorder, Long-term Disease Progression +4

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 · 284 citations · Full text

Cell Adhesion, Cellular Neurobiology, Optic Nerve +20