Andrée Robaglia‐Schlupp

Author

Also Known As

A Robaglia-Schlupp, A. Robaglia-Schlupp, A. Robaglia‐Schlupp, Andree Robaglia-Schlupp, Andrée Robaglia-Schlupp, Andrée Robaglia‐Schlupp

Publications

1.6K

Citations

H-Index

Concepts

All Affiliations

Inserm Hôpital de la Timone Hôpital de la Conception Institut de Neurobiologie de la Méditerranée Aix-Marseille Université

About

Andrée Robaglia‐Schlupp is an author at Inserm specializing in medicine, genetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	15	1.2K
2	Social Sciences	5	5	533
3	Health Sciences	2	2	84
4	Engineering	1	1	40
5	Public Health	1	1	26

Andrée Robaglia‐Schlupp

Publications

1.5K

Citations

H-Index

Page 1

	Year	Citations
Ascorbic acid treatment corrects the phenotype of a mouse model of Charcot-Marie-Tooth disease E. Passage, Jean Chrétien Norreel, Pauline Noack-Fraissignes, Nature Medicine Charcot-marie-tooth DiseaseMedicinePhysiologyPathogenesisAscorbic Acid Treatment	2004	340
SRPX2 mutations in disorders of language cortex and cognition Patrice Roll, Gabrielle Rudolf, Sandrine Pereira, Human Molecular Genetics Neurological DisorderNeurolinguisticsGeneticsSocial SciencesSylvian Fissures	2006	256
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, Human Molecular Genetics	2008	113
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, Brain NeuropsychologyNeurotransmissionEntorhinal CortexSynaptic SignalingSocial Sciences	2006	99
PMP22 overexpression causes dysmyelination in mice Andrée Robaglia‐Schlupp Brain Neurodegenerative DiseasesMolecular NeuroscienceDevelopmental BiologyMendelian DisorderGenetic Disorder	2002	79
Distribution of Calibrated Talc After Intrapleural Administration A. Fraticelli, Andrée Robaglia‐Schlupp, Helene Riera, CHEST Journal Intrapleural AdministrationLower Limb TraumaInterventional RadiologySurgeryClinical Chemistry	2002	73
Molecular evolution of the human SRPX2 gene that causes brain disorders of the Rolandic and Sylvian speech areas Barbara Royer, Dinesh C. Soares, Paul N. Barlow, BMC Genetics	2007	64
High prevalence of laminopathies among patients with metabolic syndrome Anne Dutour, Patrice Roll, Bénédicte Gaborit, Human Molecular Genetics Metabolic DisorderGeneticsPathologyMolecular GeneticsDisease Gene Identification	2011	62
Increase in mRNAs encoding neonatal II and III sodium channel α-isoforms during kainate-induced seizures in adult rat hippocampus Marguerite Gastaldi, Fabrice Bartoloméi, Annick Massacrier, Molecular Brain Research Synaptic TransmissionNeurotransmissionCellular NeurobiologySynaptic SignalingSocial Sciences	1997	60
New human sodium/glucose cotransporter gene (KST1): identification, characterization, and mutation analysis in ICCA (infantile convulsions and choreoathetosis) and BFIC (benign familial infantile convulsions) families Patrice Roll, Annick Massacrier, Sandrine Pereira, Gene Allelic VariantDevelopmental BiologyMolecular PhysiologyCotransporter GeneInfantile Convulsions	2002	55

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