Emerging major synaptic signaling pathways involved in intellectual disability von Pavlowsky, A, Chelly, J, Billuart, P

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Continuous peripheral nerve blocks in acute pain management von Chelly, J.E., Ghisi, D, Fanelli, A

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Quality of sleep among healthcare workers treating patients with coronavirus disease-19 von Omrane, A., Touil, I., Sghaier, E., Jaoued, O., Chelly, J., EL Arbi, F., Fkih Hassen, M., Mergheli, S., Knani, J., Khalfallah, T.

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Single-dose aprepitant vs ondansetron for the prevention of postoperative nausea and vomiting: a randomized, double-blind Phase III trial in patients undergoing open abdominal surg... von Diemunsch, P., Gan, T.J., Philip, B.K., Girao, M.J., Eberhart, L., Irwin, M.G., Pueyo, J., Chelly, J.E., Carides, A.D., Reiss, T., Evans, J.K., Lawson, F.C.

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Automated detection and quantification of reverse triggering effort under mechanical ventilation von Pham, Tai, Montanya, Jaume, Telias, Irene, Piraino, Thomas, Magrans, Rudys, Coudroy, Remi, Damiani, L. Felipe, Artigas, Ricard Mellado, Madorno, Matias, Blanch, Lluis, Brochard, Laurent

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Unravelling the etiology of sporadic late-onset cerebellar ataxia in a cohort of 205 patients: a prospective study von Bogdan, T., Wirth, T., Iosif, A., Schalk, A., Montaut, S., Bonnard, C., Carre, G., Lagha-Boukbiza, O., Reschwein, C., Albugues, E., Demuth, S., Landsberger, H., Einsiedler, M., Parratte, T., Nguyen, A., Lamy, F., Durand, H., Fahrer, P., Voulleminot, P., Bigaut, K., Chanson, J. B., Nicolas, G., Chelly, J., Cazeneuve, C., Koenig, M., Bund, C., Namer, I. J., Kremer, S., Calmels, N., Tranchant, C., Anheim, M.

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Novel anoctamin-3 missense mutation responsible for early-onset myoclonic dystonia von Delamarre, A., Chelly, J., Guehl, D., Drouot, N., Tranchant, C., Anheim, M., Burbaud, P.

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Do continuous ‘lumbar plexus’ blocks really increase the risk of falls? von Chelly, J.E.

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Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism von Laumonnier, F, Shoubridge, C, Antar, C, Nguyen, L S, Van Esch, H, Kleefstra, T, Briault, S, Fryns, J P, Hamel, B, Chelly, J, Ropers, H H, Ronce, N, Blesson, S, Moraine, C, Gécz, J, Raynaud, M

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Severe early-onset impulsive compulsive behavior and psychosis in PLA2G6-related juvenile Parkinson's disease von Wirth, T., Weibel, S., Montaut, S., Bigaut, K., Rudolf, G., Chelly, J., Tranchant, C., Anheim, M.

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Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression von Daoud, Fatma, Angeard, Nathalie, Demerre, Bénédicte, Martie, Itxaso, Benyaou, Rabah, Leturcq, France, Cossée, Mireille, Deburgrave, Nathalie, Saillour, Yoann, Tuffery, Sylvie, Urtizberea, Andoni, Toutain, Annick, Echenne, Bernard, Frischman, Martine, Mayer, Michèle, Desguerre, Isabelle, Estournet, Brigitte, Réveillère, Christian, Penisson-Besnier, Cuisset, Jean Marie, Kaplan, Jean Claude, Héron, Delphine, Rivier, François, Chelly, Jamel

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Paroxysmal dyskinesia: When a PRRT2 variant hides a curable cause von Schneider, V., Ferrari-Henquinet, M., Diallo, A.O., Chelly, J., Anheim, M., Tranchant, C.

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Benign hereditary chorea: From benign to serious von Lamiral, A., El Chehadeh, S., Chelly, J., Anheim, M., Laugel, V., Tranchant, C.

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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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Mutations in PHF8 are associated with X linked mental retardation and cleft lip/cleft palate von Laumonnier, F, Holbert, S, Ronce, N, Faravelli, F, Lenzner, S, Schwartz, C E, Lespinasse, J, Van Esch, H, Lacombe, D, Goizet, C, Phan-Dinh Tuy, F, van Bokhoven, H, Fryns, J-P, Chelly, J, Ropers, H-H, Moraine, C, Hamel, B C J, Briault, S

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(408) Associations of psychosocial factors with chronic postsurgical pain following total knee arthroplasty von Greco, C, Belfer, I, Vulakovich, K, Landsittel, D, Dai, F, Chelly, J

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Major synaptic signaling pathways involved in intellectual disability von Pavlowsky, A, Chelly, J, Billuart, P

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International normalized ratio and prothrombin time values before the removal of a lumbar plexus catheter in patients receiving warfarin after total hip replacement von Chelly, J.E., Szczodry, D.M., Neumann, K.J.

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Two affected boys in a Rett syndrome family: Clinical and molecular findings von VILLARD, L, KPEBE, A, CARDOSO, C, CHELLY, J, TARDIEU, M, FONTES, M

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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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