SRPX2 mutations in disorders of language cortex and cognition
Roll, Patrice, Rudolf, Gabrielle, Pereira, Sandrine, Royer, Barbara, Scheffer, Ingrid E., Massacrier, Annick, Valenti, Maria-Paola, Roeckel-Trevisiol, Nathalie, Jamali, Sarah, Beclin, Christophe, Seegmuller, Caroline, Metz-Lutz, Marie-Noëlle, Lemainque, Arnaud, Delepine, Marc, Caloustian, Christophe, Martin, Anne de Saint, Bruneau, Nadine, Depétris, Danièle, Mattéi, Marie-Geneviève, Flori, Elisabeth, Robaglia-Schlupp, Andrée, Lévy, Nicolas, Neubauer, Bernd A., Ravid, Rivka, Marescaux, Christian, Berkovic, Samuel F., Hirsch, Edouard, Lathrop, Mark, Cau, Pierre, Szepetowski, Pierre
Published in Human molecular genetics (01.04.2006)
Published in Human molecular genetics (01.04.2006)
Get full text
Journal Article
Large-scale expression study of human mesial temporal lobe epilepsy: evidence for dysregulation of the neurotransmission and complement systems in the entorhinal cortex
Jamali, Sarah, Bartolomei, Fabrice, Robaglia-Schlupp, Andrée, Massacrier, Annick, Peragut, Jean-Claude, Régis, Jean, Dufour, Henri, Ravid, Rivka, Roll, Patrice, Pereira, Sandrine, Royer, Barbara, Roeckel-Trevisiol, Nathalie, Fontaine, Marc, Guye, Maxime, Boucraut, José, Chauvel, Patrick, Cau, Pierre, Szepetowski, Pierre
Published in Brain (London, England : 1878) (01.03.2006)
Published in Brain (London, England : 1878) (01.03.2006)
Get full text
Journal Article
Regulation of calcium channel alpha(1A) subunit splice variant mRNAs in kainate-induced temporal lobe epilepsy
Vigues, S, Gastaldi, M, Chabret, C, Massacrier, A, Cau, P, Valmier, J
Published in Neurobiology of disease (01.08.1999)
Published in Neurobiology of disease (01.08.1999)
Get full text
Journal Article
PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine
Cloarec, Robin, Bruneau, Nadine, Rudolf, Gabrielle, Massacrier, Annick, Salmi, Manal, Bataillard, Marc, Boulay, Clotilde, Caraballo, Roberto, Fejerman, Natalio, Genton, Pierre, Hirsch, Edouard, Hunter, Alasdair, Lesca, Gaetan, Motte, Jacques, Roubertie, Agathe, Sanlaville, Damien, Wong, Sau-Wei, Fu, Ying-Hui, Rochette, Jacques, Ptácek, Louis J, Szepetowski, Pierre
Published in Neurology (20.11.2012)
Published in Neurology (20.11.2012)
Get more information
Journal Article
Regulation of Calcium Channel α1A Subunit Splice Variant mRNAs in Kainate-Induced Temporal Lobe Epilepsy
Vigues, S, Gastaldi, M, Chabret, C, Massacrier, A, Cau, P, Valmier, J
Published in Neurobiology of disease (01.08.1999)
Published in Neurobiology of disease (01.08.1999)
Get full text
Journal Article
The correlation between Na+ channel subunits and scorpion toxin-binding sites. A study in rat brain synaptosomes and in brain neurons developing in vitro
Jover, E, Massacrier, A, Cau, P, Martin, M F, Couraud, F
Published in The Journal of biological chemistry (25.01.1988)
Published in The Journal of biological chemistry (25.01.1988)
Get full text
Journal Article
Effect of gamma knife radiosurgery on rat brain sodium channel subunit mRNA expression
Bartolomei, F, Massacrier, A, Rey, M, Viale, M, Régis, J, Gastaldi, M, Cau, P
Published in Stereotactic and functional neurosurgery (01.01.1998)
Published in Stereotactic and functional neurosurgery (01.01.1998)
Get more information
Journal Article
Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome
MUSCATELLI, Francoise, DJOHER NORA ABROUS, MASSACRIER, Annick, BOCCACCIO, Irène, LE MOAL, Michel, CAU, Pierrre, CREMER, Harold
Published in Human molecular genetics (12.12.2000)
Published in Human molecular genetics (12.12.2000)
Get full text
Journal Article
The human necdin gene, NDN , is maternally imprinted and located in the Prader-Willi syndrome chromosomal region
Bergé Lefranc, Jean-Louis, Mattel, Marie-Geneviève, Malzac, Perrine, Jay, Philippe, Cau, Pierre, Berta, Philippe, Taviaux, Sylvie, Lalande, Marc, Rougeulle, Claire, Massacrier, Annick, Moncla, Anne, Roëckel, Nathalie, Muscatelli, Françoise
Published in Nature genetics (01.11.1997)
Published in Nature genetics (01.11.1997)
Get full text
Journal Article
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
Roll, Patrice, Massacrier, Annick, Pereira, Sandrine, Robaglia-Schlupp, Andrée, Cau, Pierre, Szepetowski, Pierre
Published in Gene (20.02.2002)
Published in Gene (20.02.2002)
Get full text
Journal Article
Nuclear localization of a novel human syntaxin 1B isoform
Pereira, Sandrine, Massacrier, Annick, Roll, Patrice, Vérine, Alain, Etienne-Grimaldi, Marie-Christine, Poitelon, Yannick, Robaglia-Schlupp, Andrée, Jamali, Sarah, Roeckel-Trevisiol, Nathalie, Royer, Barbara, Pontarotti, Pierre, Lévêque, Christian, Seagar, Michael, Lévy, Nicolas, Cau, Pierre, Szepetowski, Pierre
Published in Gene (01.11.2008)
Published in Gene (01.11.2008)
Get full text
Journal Article
mRNA coding for voltage-gated sodium channel beta 2 subunit in rat central nervous system: cellular distribution and changes following kainate-induced seizures
Gastaldi, M, Robaglia-Schlupp, A, Massacrier, A, Planells, R, Cau, P
Published in Neuroscience letters (12.06.1998)
Published in Neuroscience letters (12.06.1998)
Get full text
Journal Article