Refinement of cortical dysgeneses spectrum associated with TUBA1A mutations von Bahi-Buisson, N, Poirier, K, Boddaert, N, Saillour, Y, Castelnau, L, Philip, N, Buyse, G, Villard, L, Joriot, S, Marret, S, Bourgeois, M, Van Esch, H, Lagae, L, Amiel, J, Hertz-Pannier, L, Roubertie, A, Rivier, F, Pinard, J M, Beldjord, C, Chelly, J

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Doublecortin Is the Major Gene Causing X-Linked Subcortical Laminar Heterotopia (SCLH) von 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

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Callosotomy for Epilepsy After West Syndrome von Pinard, J. M., Delalande, O., Chiron, C., Soufflet, C., Plouin, P., Kim, Y., Dulac, O.

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Functional MRI in double cortex : Functionality of heterotopia von PINARD, J.-M, FEYDY, A, CARLIER, R, PEREZ, N, PIEROT, L, BURNOD, Y

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A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome von Portes, Vincent des, Pinard, Jean Marc, Billuart, Pierre, Vinet, Marie Claude, Koulakoff, Annette, Carrié, Alain, Gelot, Antoinette, Dupuis, Elisabeth, Motte, Jacques, Berwald-Netter, Yoheved, Catala, Martin, Kahn, Axel, Beldjord, Cherif, Chelly, Jamel

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Subcortical laminar heterotopia and lissencephaly in two families: a single X linked dominant gene von Pinard, J M, Motte, J, Chiron, C, Brian, R, Andermann, E, Dulac, O

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X-linked malformations of neuronal migration von Dobyns, W. B., Andermann, E., Andermann, F., Czapansky-Beilman, D., Dubeau, F., Dulac, O., Guerrini, R., Hirsch, B., Ledbetter, D. H., Lee, N. S., Motte, J., Pinard, J.-M., Radtke, R. A., Ross, M. E., Tampieri, D., Walsh, C. A., Truwit, C. L.

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Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22 von des Portes, V, Pinard, J M, Smadja, D, Motte, J, Boespflüg-Tanguy, O, Moutard, M L, Desguerre, I, Billuart, P, Carrie, A, Bienvenu, T, Vinet, M C, Bachner, L, Beldjord, C, Dulac, O, Kahn, A, Ponsot, G, Chelly, J

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Manifestations neurologiques de la maladie de Fabry von Clavelou, P., Besson, G., Elziere, C., Ferrier, A., Pinard, J.-M., Hermier, M., Artigou, J.Y., Germain, D.P.

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So-called 'cryptogenic' partial seizures resulting from a subtle cortical dysgenesis due to a doublecortin gene mutation von des Portes, V, Abaoub, L, Joannard, A, Souville, I, Francis, F, Pinard, J M, Chelly, J, Beldjord, C, Jouk, P S

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Phenotype and genotype in 101 males with X-linked creatine transporter deficiency von van de Kamp, J M, Betsalel, O T, Mercimek-Mahmutoglu, S, Abulhoul, L, Grünewald, S, Anselm, I, Azzouz, H, Bratkovic, D, de Brouwer, A, Hamel, B, Kleefstra, T, Yntema, H, Campistol, J, Vilaseca, M A, Cheillan, D, D’Hooghe, M, Diogo, L, Garcia, P, Valongo, C, Fonseca, M, Frints, S, Wilcken, B, von der Haar, S, Meijers-Heijboer, H E, Hofstede, F, Johnson, D, Kant, S G, Lion-Francois, L, Pitelet, G, Longo, N, Maat-Kievit, J A, Monteiro, J P, Munnich, A, Muntau, A C, Nassogne, M C, Osaka, H, Ounap, K, Pinard, J M, Quijano-Roy, S, Poggenburg, I, Poplawski, N, Abdul-Rahman, O, Ribes, A, Arias, A, Yaplito-Lee, J, Schulze, A, Schwartz, C E, Schwenger, S, Soares, G, Sznajer, Y, Valayannopoulos, V, Van Esch, H, Waltz, S, Wamelink, M M C, Pouwels, P J W, Errami, A, van der Knaap, M S, Jakobs, C, Mancini, G M, Salomons, G S

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X-linked malformations of neuronal migration von Dobyns, W B, Andermann, E, Andermann, F, Czapansky-Beilman, D, Dubeau, F, Dulac, O, Guerrini, R, Hirsch, B, Ledbetter, D H, Lee, N S, Motte, J, Pinard, J M, Radtke, R A, Ross, M E, Tampieri, D, Walsh, C A, Truwit, C L

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Subcortical Laminar Heterotopia in Two Sisters and Their Mother: MRI, Clinical Findings and Pathogenesis von van der Valk, P. H., Snoeck, I., Meiners, L. C., des Portes, V., Chelly, J., Pinard, J. -M., Ippel, P. F., van Nieuwenhuizen, O., Peters, A. C.

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Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders von Travaglini, Lorena, Brancati, Francesco, Silhavy, Jennifer, Iannicelli, Miriam, Nickerson, Elizabeth, Elkhartoufi, Nadia, Scott, Eric, Spencer, Emily, Gabriel, Stacey, Thomas, Sophie, Ben-Zeev, Bruria, Bertini, Enrico, Boltshauser, Eugen, Chaouch, Malika, Cilio, Maria Roberta, de Jong, Mirjam M, Kayserili, Hulya, Ogur, Gonul, Poretti, Andrea, Signorini, Sabrina, Uziel, Graziella, Zaki, Maha S, Johnson, Colin, Attié-Bitach, Tania, Gleeson, Joseph G, Valente, Enza Maria

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Neurological aspects of Fabry's disease von Clavelou, P, Besson, G, Elziere, C, Ferrier, A, Pinard, J-M, Hermier, M, Artigou, J Y, Germain, D P

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Résultats cliniques et neuropsychologiques à long terme après hémisphérotomie von Bulteau, C, Delalande, O, Buret, V, Jalin, C, Fohlen, M, Pinard, J.M, Jambaqué, I, Dulac, O, Dellatolas, G

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Retard mental et troubles de la corticogenèse von Portes, V. Des, Pinard, J.M., Francis, F., Beldjord, C., Ponsot, G., Chelly, J.

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Sleep Disorders Caused by Brainstem Tumor: Case Report von Ioos, Christine, Estournet-Mathiaud, Brigitte, Pinard, Jean-Marc, Cheliout-Héraut, Fawzia

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De novo t(X;21)(q28;q11) in a girl with phenotypic features of Williams-Beuren syndrome von Telvi, L, Pinard, J M, Ion, R, Sinet, P M, Nicole, A, Feingold, J, Dulac, O, Pompidou, A, Ponsot, G

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Indications de la chirurgie de l'épilepsie chez l'enfant von Fohlen, M, Delalande, O, Pinard, JM, Dulac, O

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