Heterogeneity in defining fetal corpus callosal pathology: systematic review von Mahallati, H., Sotiriadis, A., Celestin, C., Millischer, A. E., Sonigo, P., Grevent, D., O'Gorman, N., Bahi‐Buisson, N., Attié‐Bitach, T., Ville, Y., Salomon, L. J.

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Fetal brain imaging following laser surgery in twin‐to‐twin surgery von Stirnemann, J, Chalouhi, G, Essaoui, M, Bahi‐Buisson, N, Sonigo, P, Millischer, A‐E, Lapillonne, A, Guigue, V, Salomon, LJ, Ville, Y

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Clinical, functional and genetic characterization of 16 patients suffering from chronic granulomatous disease variants – identification of 11 novel mutations in CYBB von Mollin, M., Beaumel, S., Vigne, B., Brault, J., Roux‐Buisson, N., Rendu, J., Barlogis, V., Catho, G., Dumeril, C., Fouyssac, F., Monnier, D., Gandemer, V., Revest, M., Brion, J.‐P., Bost‐Bru, C., Jeziorski, E., Eitenschenck, L., Jarrasse, C., Drillon Haus, S., Houachée‐Chardin, M., Hancart, M., Michel, G., Bertrand, Y., Plantaz, D., Kelecic, J., Traberg, R., Kainulainen, L., Fauré, J., Fieschi, F., Stasia, M. J.

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CDKL5-Related Disorders: From Clinical Description to Molecular Genetics von Bahi-Buisson, N., Bienvenu, T.

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Homozygous PKP2 deletion associated with neonatal left ventricle noncompaction von Ramond, F., Janin, A., Di Filippo, S., Chanavat, V., Chalabreysse, L., Roux‐Buisson, N., Sanlaville, D., Touraine, R., Millat, G.

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Distinguishing Recurrent Thyroid Cancer from Residual Nonmalignant Thyroid Tissue Using Multiphasic Multidetector CT von Debnam, J. M., Guha-Thakurta, N., Sun, J., Wei, W., Zafereo, M. E., Cabanillas, M. E., Buisson, N. M., Schellingerhout, D.

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Identification of variants of the ryanodine receptor type 1 in patients with exertional heat stroke and positive response to the malignant hyperthermia in vitro contracture test von Roux-Buisson, N, Monnier, N, Sagui, E, Abriat, A, Brosset, C, Bendahan, D, Kozak-Ribbens, G, Gazzola, S, Quesada, J.-L., Foutrier-Morello, C, Rendu, J, Figarella-Branger, D, Cozonne, P, Aubert, M, Bourdon, L, Lunardi, J, Fauré, J

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Feasibility and Added Value of Fetal DTI Tractography in the Evaluation of an Isolated Short Corpus Callosum: Preliminary Results von Millischer, A-E, Grevent, D, Sonigo, P, Bahi-Buisson, N, Desguerre, I, Mahallati, H, Bault, J-P, Quibel, T, Couderc, S, Moutard, M-L, Julien, E, Dangouloff, V, Bessieres, B, Malan, V, Attie, T, Salomon, L-J, Boddaert, N

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Clinical characteristics of COVID-19 infection in polyhandicapped persons in France von Rousseau, M.-C., Hully, M., Milh, M., Juzeau, D., Pollez, B., Peudenier, S., Bahi Buisson, N., Gautheron, V., Chabrol, B., Billette de Villemeur, T.

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Effects of ganaxolone on non-seizure outcomes in CDKL5 Deficiency Disorder: Double-blind placebo-controlled randomized trial von Downs, J., Jacoby, P., Specchio, N., Cross, H., Amin, S., Bahi-Buisson, N., Rajaraman, R., Suter, B., Devinsky, O., Aimetti, A., Busse, G., Olson, H.E., Demarest, S., Benke, T.A., Pestana-Knight, E.

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Survenue d’une crise d’épilepsie prolongée chez l’enfant : quelle prise en charge en dehors du milieu hospitalier ? von Arzimanoglou, A., Wait, S., Auvin, S., Bahi-Buisson, N., Nguyen, S.

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FOXG1-Related Disorders: From Clinical Description to Molecular Genetics von Florian, C., Bahi-Buisson, N., Bienvenu, T.

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The Tomb of the Three Brothers in Palmyra: The Use of Mimetite, A Rare Yellow Pigment, in A Rich Decoration von Buisson, N., Burlot, D., Eristov, H., Eveno, M., Sarkis, N.

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Electro-clinical features in epileptic children with chromosome 15q duplication syndrome von Dangles, M.-T., Malan, V., Dumas, G., Romana, S., Raoul, O., Coste-Zeitoun, D., Soufflet, C., Vignolo-Diard, P., Bahi-Buisson, N., Barnérias, C., Chemaly, N., Desguerre, I., Gitiaux, C., Hully, M., Bourgeois, M., Guimier, A., Rio, M., Munnich, A., Nabbout, R., Kaminska, A., Eisermann, M.

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Outcome of childhood-onset epilepsy from adolescence to adulthood: Transition issues von Nabbout, R, Andrade, D.M, Bahi-Buisson, N, Cross, H, Desquerre, I, Dulac, O, Granata, T, Hirsch, E, Navarro, V, Ouss, L, Pearl, P.L, Schmidt, D, Thiele, E, Camfield, P.R, Camfield, C.S

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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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Updating the profile of C-terminal MECP2 deletions in Rett syndrome von Bebbington, A, Percy, A, Christodoulou, J, Ravine, D, Ho, G, Jacoby, P, Anderson, A, Pineda, M, Ben Zeev, B, Bahi-Buisson, N, Smeets, E, Leonard, H

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Cell cloning‐based transcriptome analysis in Rett patients: relevance to the pathogenesis of Rett syndrome of new human MeCP2 target genes von Nectoux, J., Fichou, Y., Rosas‐Vargas, H., Cagnard, N., Bahi‐Buisson, N., Nusbaum, P., Letourneur, F., Chelly, J., Bienvenu, T.

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Two new cases of serine deficiency disorders treated with l -serine von Brassier, A, Valayannopoulos, V, Bahi-Buisson, N, Wiame, Elsa, Hubert, L, Boddaert, N, Kaminska, A, Habarou, F, Desguerre, I, Van Schaftingen, E, Ottolenghi, C, de Lonlay, P

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Myoclonus-dystonia : Clinical and electrophysiologic pattern related to SGCE mutations von ROZE, E, APARTIS, E, ANDRE-OBADIA, N, MALTETE, D, ECHANIZ-LAGUNA, A, PEREON, Y, BEAUGENDRE, Y, DUPONT, S, DE GRESLAN, T, JEDYNAK, C. P, PONSOT, G, DUSSAULE, J. C, CLOT, F, BRICE, A, DÜRR, A, VIDAILHET, M, DORISON, N, THOBOIS, S, GUYANT-MARECHAL, L, TRANCHANT, C, DAMIER, P, DOUMMAR, D, BAHI-BUISSON, N

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