检索结果 - G Ponsot

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  1. 1
    Limits of Early Diagnosis of Herpes Simplex Encephalitis in Children: A Retrospective Study of 38 Cases

    Limits of Early Diagnosis of Herpes Simplex Encephalitis in Children: A Retrospective Study of 38 Cases 由 Xavier De Tiège, Bénédicte Héron, Pierre Lebon, G Ponsot, Flore Rozenberg

    出版 2003
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  2. 2
    Reappraisal of Rasmussen's syndrome with special emphasis on treatment with high doses of steroids.

    Reappraisal of Rasmussen's syndrome with special emphasis on treatment with high doses of steroids. 由 D. Chinchilla, Olivier Dulac, O. Robain, P. Plouin, G Ponsot, J Pinel, Doris Α. Graber

    出版 1994
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  3. 3
    Pyruvate dehydrogenase complex deficiency: four neurological phenotypes with differing pathogenesis

    Pyruvate dehydrogenase complex deficiency: four neurological phenotypes with differing pathogenesis 由 Christine Barnérias, Jean‐Marie Saudubray, Guy Touati, Pascale de Lonlay, Olivier Dulac, G Ponsot, C. Marsac, M. Brivet, Isabelle Desguerre

    出版 2009
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  4. 4
    Doublecortin Is the Major Gene Causing X-Linked Subcortical Laminar Heterotopia (SCLH)

    Doublecortin Is the Major Gene Causing X-Linked Subcortical Laminar Heterotopia (SCLH) 由 V. des Portes, Fiona Francis, J.-M. Pinard, Isabelle Desguerre, M.L. Moutard, I. Snoeck, Linda C. Meiners, F. Capron, Raffaella Cusmai, Stefano Ricci, J. Motte, B. Echenne, G Ponsot, Olivier Dulac, J. Chelly, C. Beldjord

    出版 1998
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  5. 5
    Infantile Alexander Disease: Spectrum of GFAP Mutations and Genotype-Phenotype Correlation

    Infantile Alexander Disease: Spectrum of GFAP Mutations and Genotype-Phenotype Correlation 由 Diana Rodriguez, Fernande Gauthier, Enrico Bertini, Marianna Bugiani, Michael Brenner, Sylvie Nguyen, Cyril Goizet, A. Gélot, Robert Surtees, Jean‐Michel Pédespan, X. Hernandoréna, M. Troncoso, G. Uziel, Albee Messing, G Ponsot, Danielle Pham-Dinh, André Dautigny, Odile Boespflug‐Tanguy

    出版 2001
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  6. 6
    Recurrence of the T666M Calcium Channel CACNA1A Gene Mutation in Familial Hemiplegic Migraine with Progressive Cerebellar Ataxia

    Recurrence of the T666M Calcium Channel CACNA1A Gene Mutation in Familial Hemiplegic Migraine with Progressive Cerebellar Ataxia 由 Anne Ducros, Christian Denier, Anne Joutel, Katayoun Vahedi, A. Michel, Françoise Darcel, M Madigand, Djelloul Guerouaou, François Tison, Jean‐Philippe Julien, Étienne C. Hirsch, F Chédru, C Bisgård, G Lucotte, Philippe Desprès, C. Billard, M.‐A. Barthez, G Ponsot, M.G. Bousser, Elisabeth Tournier‐Lasserve

    出版 1999
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  7. 7
    Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes

    Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes 由 Sophie Tézenas du Montcel, F. Clot, M. Vidailhet, Emmanuel Roze, Philippe Damier, C P Jedynak, A. Camuzat, A Lagueny, Laurent Vercueil, Diane Doummar, Lucie Guyant‐Maréchal, J.L. Houéto, G Ponsot, Stéphane Thobois, Marie‐Anne Cournelle, Alexandra Dürr, Franck Durif, Bernard Échenne, Didier Hannequin, Christine Tranchant, Alexis Brice

    出版 2005
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  8. 8
    Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia

    Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia 由 F. Clot, David Grabli, C. Cazeneuve, Emmanuel Roze, Pierre Castelnau, B. Chabrol, P. Landrieu, Karine Nguyen, G Ponsot, Myriem Abada, Diane Doummar, Philippe Damier, R. Gil, Stéphane Thobois, Alana Ward, Michael Hutchinson, Annick Toutain, Fabienne Picard, A. Camuzat, Estelle Fédirko, Chann San, Delphine Bouteiller, Eric LeGuern, Alexandra Dürr, Marie Vidailhet, Alexis Brice

    出版 2009
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