BDNF and LTP-/LTD-like plasticity of the primary motor cortex in Gilles de la Tourette syndrome von Marsili, L., Suppa, A., Di Stasio, F., Belvisi, D., Upadhyay, N., Berardelli, I., Pasquini, M., Petrucci, S., Ginevrino, M., Fabbrini, G., Cardona, F., Defazio, G., Berardelli, A.

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The National Italian Guidelines on the diagnosis and treatment of children with pediatric ataxias von Lacorte, Eleonora, Piscopo, Paola, Sagliocca, Luciano, Vignatelli, Luca, Taruscio, Domenica, Vanacore, Nicola

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Absence of FGFR3–TACC3 rearrangement in hematological malignancies with numerical chromosomal alteration von Banella, C., Ginevrino, M., Catalano, G., Fabiani, E., Falconi, G., Divona, M., Curzi, P., Panetta, P., Voso, M.T., Noguera, N.I.

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Les mutations gain de fonction de TLR7 sont à l’origine d’une maladie systémique et neuro-inflammatoire von David, C., Badony, M., Kechiche, R., Insalaco, A., Zecca, M., De Benedetti, F., Orcesi, S., Chiapparini, L., Comoli, P., Federici, S., Gattorno, M., Ginevrino, M., Giorgio, E., Matteo, V., Moran-alvarez, P., Politano, D., Giusi, P., Fabio, S., Volpi, S., Masson, C., Rice, G., Frémond, M.L., Lepelley, A., Marsch, J., Crow, Y.

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Generation of two human induced pluripotent stem cell (hiPSC) lines from a long QT syndrome South African founder population von Mura, Manuela, Pisano, Federica, Stefanello, Manuela, Ginevrino, Monia, Boni, Marina, Calabrò, Federica, Crotti, Lia, Valente, Enza Maria, Schwartz, Peter J., Brink, Paul A., Gnecchi, Massimiliano

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Absence of FGFR3-TACC3 rearrangement in hematological malignancies with numerical chromosomal alteration von Banella, C, Ginevrino, M, Catalano, G, Fabiani, E, Falconi, G, Divona, M, Curzi, P, Panetta, P, Voso, M T, Noguera, N I

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Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease von Blauwendraat, Cornelis, Reed, Xylena, Kia, Demis A, Gan-Or, Ziv, Lesage, Suzanne, Pihlstrøm, Lasse, Guerreiro, Rita, Gibbs, J. Raphael, Sabir, Marya, Ahmed, Sarah, Ding, Jinhui, Alcalay, Roy N, Hassin-Baer, Sharon, Pittman, Alan M, Brooks, Janet, Edsall, Connor, Hernandez, Dena G, Chung, Sun Ju, Goldwurm, Stefano, Toft, Mathias, Schulte, Claudia, Bras, Jose, Wood, Nicholas W, Brice, Alexis, Morris, Huw R, Scholz, Sonja W, Nalls, Mike A, Singleton, Andrew B, Cookson, Mark R

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Clinical variability at the mild end of BRAT1‐related spectrum: Evidence from two families with genotype–phenotype discordance von Nuovo, Sara, Baglioni, Valentina, De Mori, Roberta, Tardivo, Silvia, Caputi, Caterina, Ginevrino, Monia, Micalizzi, Alessia, Masuelli, Laura, Federici, Giulia, Casella, Antonella, Lorefice, Elisa, Anello, Danila, Tolve, Manuela, Farini, Donatella, Bertini, Enrico, Zanni, Ginevra, Travaglini, Lorena, Vasco, Gessica, Sette, Claudio, Carducci, Carla, Valente, Enza M., Leuzzi, Vincenzo

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APP‐Related Corticobasal Syndrome: Expanding the List of Corticobasal Degeneration Look Alikes von Abate, Filomena, Dati, Giovanna, Ginevrino, Monia, Valente, Enza M., Barone, Paolo, Picillo, Marina

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Age and sex prevalence estimate of Joubert syndrome in Italy von Nuovo, Sara, Bacigalupo, Ilaria, Ginevrino, Monia, Battini, Roberta, Bertini, Enrico, Borgatti, Renato, Casella, Antonella, Micalizzi, Alessia, Nardella, Marta, Romaniello, Romina, Serpieri, Valentina, Zanni, Ginevra, Valente, Enza Maria, Vanacore, Nicola

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Determinants of 6-month mortality in survivors of myocardial infarction after thrombolysis : results of the GISSI-2 data base von VOLPI, A, DE VITA, C, FRANZOSI, M. G, GERACI, E, MAGGIONI, P, MAURI, F, NEGRI, E, SANTORO, E, TAVAZZI, L, TOGNONI, G

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APP-Related Corticobasal Syndrome: Expanding the List of Corticobasal Degeneration Look Alikes von Abate, Filomena, Dati, Giovanna, Ginevrino, Monia, Valente, Enza M, Barone, Paolo, Picillo, Marina

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