Andrée Robaglia‐Schlupp

Ascorbic acid treatment corrects the phenotype of a mouse model of Charcot-Marie-Tooth disease

E. Passage, Jean Chrétien Norreel, Pauline Noack-Fraissignes et al. · Nature Medicine · 2004 · 340 citations

Charcot-marie-tooth Disease, Medicine, Physiology +7

SRPX2 mutations in disorders of language cortex and cognition

Patrice Roll, Gabrielle Rudolf, Sandrine Pereira et al. · Human Molecular Genetics · 2006 · 256 citations

Neurological Disorder, Neurolinguistics, Genetics +17

Epileptic and developmental disorders of the speech cortex: ligand/receptor interaction of wild-type and mutant SRPX2 with the plasminogen activator receptor uPAR

Barbara Royer-Zemmour, Magali Ponsole-Lenfant, Hyam Gara et al. · Human Molecular Genetics · 2008 · 113 citations · Full text

Large-scale expression study of human mesial temporal lobe epilepsy: evidence for dysregulation of the neurotransmission and complement systems in the entorhinal cortex

Sarah Jamali, Fabrice Bartoloméi, Andrée Robaglia‐Schlupp et al. · Brain · 2006 · 99 citations · Full text

Neuropsychology, Neurotransmission, Entorhinal Cortex +22

PMP22 overexpression causes dysmyelination in mice

Andrée Robaglia‐Schlupp · Brain · 2002 · 79 citations · Full text

Neurodegenerative Diseases, Molecular Neuroscience, Developmental Biology +15