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Bonthron, David T, Lindahl, Tomas, Ali, Manir, Ponsot, Gerard, Robins, Peter, Voit, Thomas, van Bokhoven, Hans, Barnes, Deborah E, Livingston, John H, Massey, Roger F, Crow, Yanick J, Parmar, Rekha, Lebon, Pierre, Jackson, Andrew P, Hayward, Bruce E, Hamel, Ben C, Leitch, Andrea, Klepper, Joerg, Cowan, Frances M, Frints, Suzanne G, Black, Deborah N, Lynch, Sally Ann, Meritet, Jean François, Brunner, Han G, Corry, Peter C, Michaud, Jacques L
Published in Nature genetics (01.08.2006)
Published in Nature genetics (01.08.2006)
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Evidence against haploinsuffiency of human ataxin 10 as a cause of spinocerebellar ataxia type 10
Keren, Boris, Jacquette, Aurélia, Depienne, Christel, Leite, Patricia, Durr, Alexandra, Carpentier, Wassila, Benyahia, Baya, Ponsot, Gerard, Soubrier, Florent, Brice, Alexis, Héron, Delphine
Published in Neurogenetics (01.05.2010)
Published in Neurogenetics (01.05.2010)
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MRI prognostic factors for relapse after acute CNS inflammatory demyelination in childhood
Mikaeloff, Yann, Adamsbaum, Catherine, Husson, Béatrice, Vallée, Louis, Ponsot, Gérard, Confavreux, Christian, Tardieu, Marc, Suissa, Samy
Published in Brain (London, England : 1878) (01.09.2004)
Published in Brain (London, England : 1878) (01.09.2004)
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Unexplained mental retardation: is brain MRI useful?
Decobert, Fabrice, Grabar, Sophie, Merzoug, Valerie, Kalifa, Gabriel, Ponsot, Gérard, Adamsbaum, Catherine, des Portes, Vincent
Published in Pediatric radiology (01.06.2005)
Published in Pediatric radiology (01.06.2005)
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Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia
Clot, Fabienne, Grabli, David, Cazeneuve, Cécile, Roze, Emmanuel, Castelnau, Pierre, Chabrol, Brigitte, Landrieu, Pierre, Nguyen, Karine, Ponsot, Gérard, Abada, Myriem, Doummar, Diane, Damier, Philippe, Gil, Roger, Thobois, Stéphane, Ward, Alana J., Hutchinson, Michael, Toutain, Annick, Picard, Fabienne, Camuzat, Agnès, Fedirko, Estelle, Sân, Chankannira, Bouteiller, Delphine, LeGuern, Eric, Durr, Alexandra, Vidailhet, Marie, Brice, Alexis
Published in Brain (London, England : 1878) (01.07.2009)
Published in Brain (London, England : 1878) (01.07.2009)
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Pyruvate dehydrogenase complex deficiency: four neurological phenotypes with differing pathogenesis
BARNERIAS, CHRISTINE, SAUDUBRAY, JEAN‐MARIE, TOUATI, GUY, DE LONLAY, PASCALE, DULAC, OLIVIER, PONSOT, GERARD, MARSAC, CÉCILE, BRIVET, MICHÈLE, DESGUERRE, ISABELLE
Published in Developmental medicine and child neurology (01.02.2010)
Published in Developmental medicine and child neurology (01.02.2010)
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Benefit of intravenous immunoglobulin in autoimmune stiff-person syndrome in a child
Mikaeloff, Yann, Jambaque, Isabelle, Mayer, Michele, Ponsot, Gerard, Kalifa, Gabriel, Carel, Jean-Claude
Published in The Journal of pediatrics (01.08.2001)
Published in The Journal of pediatrics (01.08.2001)
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First episode of acute CNS inflammatory demyelination in childhood: prognostic factors for multiple sclerosis and disability
Mikaeloff, Yann, Suissa, Samy, Vallée, Louis, Lubetzki, Catherine, Ponsot, Gérard, Confavreux, Christian, Tardieu, Marc, KIDMUS Study Group
Published in The Journal of pediatrics (01.02.2004)
Published in The Journal of pediatrics (01.02.2004)
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Orphan drugs and orphan diseases
Campos-Castelló, Jaime, Ponsot, Gerard, Feillet, François, Vidailhet, M, Maire, Irène
Published in European journal of paediatric neurology (01.05.2000)
Published in European journal of paediatric neurology (01.05.2000)
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Agenesis of corpus callosum: prenatal diagnosis and prognosis
MOUTARD, Marie-Laure, KIEFFER, Virginie, PONSOT, Gérard, FEINGOLD, Josué, KIEFFER, Francois, LEWIN, Fanny, ADAMSBAUM, Catherine, GELOT, Antoinette, CAMPISTOL I PLANA, Jaume, VAN BOGAERT, Patrick, ANDRE, Monique
Published in Child's nervous system (01.08.2003)
Published in Child's nervous system (01.08.2003)
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Infantile Alexander Disease: Spectrum of GFAP Mutations and Genotype-Phenotype Correlation
Rodriguez, Diana, Gauthier, Fernande, Bertini, Enrico, Bugiani, Marianna, Brenner, Michael, N'guyen, Sylvie, Goizet, Cyril, Gelot, Antoinette, Surtees, Robert, Pedespan, Jean-Michel, Hernandorena, Xavier, Troncoso, Monica, Uziel, Graziela, Messing, Albee, Ponsot, Gérard, Pham-Dinh, Danielle, Dautigny, André, Boespflug-Tanguy, Odile
Published in American journal of human genetics (01.11.2001)
Published in American journal of human genetics (01.11.2001)
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Interferon-β treatment in patients with childhood-onset multiple sclerosis
Mikaeloff, Yann, Moreau, Thibault, Debouverie, Marc, Pelletier, Jean, Lebrun, Christine, Gout, Olivier, Pedespan, Jean-Michel, Van Hulle, Catherine, Vermersch, Patrick, Ponsot, Gérard
Published in The Journal of pediatrics (01.09.2001)
Published in The Journal of pediatrics (01.09.2001)
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Herpes simplex encephalitis: diagnostic problems and late relapse
De Tiège, Xavier, Rozenberg, Flore, Burlot, Karine, Gaudelus, Joël, Ponsot, Gérard, Héron, Bénédicte
Published in Developmental medicine and child neurology (01.01.2006)
Published in Developmental medicine and child neurology (01.01.2006)
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Doublecortin Is the Major Gene Causing X-Linked Subcortical Laminar Heterotopia (SCLH)
des Portes, Vincent, Francis, Fiona, Pinard, Jean-Marc, Desguerre, Isabelle, Moutard, Marie-Laure, Snoeck, Irina, Meiners, Linda C., Capron, François, Cusmai, Raffaella, Ricci, Stefano, Motte, Jacques, Echenne, Bernard, Ponsot, Gérard, Dulac, Olivier, Chelly, Jamel, Beldjord, Cherif
Published in Human molecular genetics (01.07.1998)
Published in Human molecular genetics (01.07.1998)
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