EFNS guidelines on diagnosis and treatment of primary dystonias von Albanese, A., Asmus, F., Bhatia, K. P., Elia, A. E., Elibol, B., Filippini, G., Gasser, T., Krauss, J. K., Nardocci, N., Newton, A., Valls-Solé, J.

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Pallidal stimulation for acquired dystonia due to cerebral palsy: beyond 5 years von Romito, L. M., Zorzi, G., Marras, C. E., Franzini, A., Nardocci, N., Albanese, A.

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Neurodegeneration associated with genetic defects in phospholipase A2 von GREGORY, A, WESTAWAY, S. K, RODRIGUEZ, D, DESGUERRE, I, BERTINI, E, SIMONATI, A, LEVINSON, B, DIAS, C, BARBOT, C, CARRILHO, I, SANTOS, M, MALIK, I, HOLM, I. E, GITSCHIER, J, HAYFLICK, S. J, KOTZBAUER, P. T, HOGARTH, P, SONEK, S, CORYELL, J. C, NGUYEN, T. M, NARDOCCI, N, ZORZI, G

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Globus pallidus internus activity during simultaneous bilateral microelectrode recordings in status dystonicus von Levi, Vincenzo, Franzini, A., Rinaldo, S., Coelli, S., Bianchi, A. M., Nardocci, N., Eleopra, R., Zorzi, G.

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Neurodegeneration associated with genetic defects in phospholipase A(2) von Gregory, A, Westaway, S K, Holm, I E, Kotzbauer, P T, Hogarth, P, Sonek, S, Coryell, J C, Nguyen, T M, Nardocci, N, Zorzi, G, Rodriguez, D, Desguerre, I, Bertini, E, Simonati, A, Levinson, B, Dias, C, Barbot, C, Carrilho, I, Santos, M, Malik, I, Gitschier, J, Hayflick, S J

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PAROXYSMAL MOVEMENT DISORDERS IN GLUT1 DEFICIENCY SYNDROME von ZORZI, G, CASTELLOTTI, B, ZIBORDI, F, GELLERA, C, NARDOCCI, N

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Long‐term educational program to limit the burden of neurological disorders in Sub‐Saharan Africa: report from an Italy−Mozambique cooperation on epilepsy in children von Leone, M., Sulemane, D. I., Nardocci, N., Bartolo, M., Didato, G.

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R106C TFG variant causes infantile neuroaxonal dystrophy “plus” syndrome von Catania, A., Battini, R., Pippucci, T., Pasquariello, R., Chiapparini, M. L., Seri, M., Garavaglia, B., Zorzi, G., Nardocci, N., Ghezzi, D., Tiranti, V.

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Extragenetic factors and clinical penetrance of DYT1 dystonia: an exploratory study von Martino, D., Gajos, A., Gallo, V., Cif, L., Coubes, P., Tinazzi, M., Schneider, S. A., Fiorio, M., Zorzi, G., Nardocci, N., Ben-Shlomo, Y., Edwards, M. J., Bhatia, K. P.

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Elevated aspartate aminotransferase and lactate dehydrogenase levels are a constant finding in PLA2G6-associated neurodegeneration von Kraoua, I., Romani, M., Tonduti, D., BenRhouma, H., Zorzi, G., Zibordi, F., Ardissone, A., Gouider-Khouja, N., Ben Youssef-Turki, I., Nardocci, N., Valente, E. M.

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SUSCEPTIBILITY TO DYT1 DYSTONIA IN EUROPEAN PATIENTS IS MODIFIED BY THE D216H POLYMORPHISM von KAMM, C, FISCHER, H, KUPSCH, A, NARDOCCI, N, GASSER, T, GARAVAGLIA, B, KULLMANN, S, SHARMA, M, SCHRADER, C, GRUNDMANN, K, KLEIN, C, BORGGRÄFE, I, LOBSIE, E

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P1027: Neurophysiological findings in patients with ceroid lipofuscinosis due to CLN6 mutations von Canafoglia, L, Gilioli, I, Granata, T, Binelli, S, Garavaglia, B, Berkovic, S, Nardocci, N, Franceschetti, S

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INV13 Movement disorders with video case presentations von Nardocci, N

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Hemophagocytic lymphohistiocytosis with neurological presentation: MRI findings and a nearly miss diagnosis von Chiapparini, L., Uziel, G., Vallinoto, C., Bruzzone, M. G., Rovelli, A., Tricomi, G., Bizzi, A., Nardocci, N., Rizzari, C., Savoiardo, M.

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P7.20 Bilateral, pallidal deep-brain stimulation in primary and non-primary dystonia: a prospective long-term follow-up study von Romito, L, Zorzi, G, Ciceri, M, Franzini, A, Nardocci, N, Albanese, A

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Impaired body movement representation in DYT1 mutation carriers von Fiorio, M, Gambarin, M, Defazio, G, Valente, E.M, Stanzani, C, Moretto, G, Loi, M, Soliveri, P, Nardocci, N, Albanese, A, Fiaschi, A, Tinazzi, M

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Consensus clinical management guideline for pantothenate kinase-associated neurodegeneration (PKAN) von Hogarth, Penelope, Kurian, Manju A., Gregory, Allison, Csányi, Barbara, Zagustin, Tamara, Kmiec, Tomasz, Wood, Patricia, Klucken, Angelika, Scalise, Natale, Sofia, Francesca, Klopstock, Thomas, Zorzi, Giovanna, Nardocci, Nardo, Hayflick, Susan J.

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Revelation of a Novel CLN5 Mutation in Early Juvenile Neuronal Ceroid Lipofuscinosis von Cannelli, N., Nardocci, N., Cassandrini, D., Morbin, M., Aiello, C., Bugiani, M., Criscuolo, L., Zara, F., Striano, P., Granata, T., Bertini, E., Simonati, A., Santorelli, F. M.

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Response to letter by Dr Neil Murray von Albanese, A., Asmus, F., Bhatia, K., Elia, A. E., Elibol, B., Filippini, G., Gasser, T., Krauss, J. K., Nardocci, N., Newton, A., Valls-Solé, J.

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Infantile neuroaxonal dystrophy : Clinical spectrum and diagnostic criteria von NARDOCCI, N, ZORZI, G, FARINA, L, BINELLI, S, SCAIOLI, W, CIANO, C, VERGA, L, ANGELINI, L, SAVOIARDO, M, BUGIANI, O

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