Intronic GAA-FGF14 Expansion in an italian patient presenting with early-onset cerebellar ataxia von Mitrotti, P., Avenali, M., Vegezzi, E., Zangaglia, R., Cortese, A., Currò, R., Pellerin, D., Dicaire, M.-J., Brais, B., Palmieri, I., Gana, S., Valente, E.M.

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Interaction between sex and GBA mutations influences clinical phenotype in Parkinson disease von Gallo, L., Avenali, M., Caminiti, S., Mitrotti, P., Pocora, M., Cuconato, G., Palmieri, I., Pasquini, C., Galandra, C., Calabrese, R., Zangaglia, R., Tassorelli, C., Schapira, A.V.H., Valente, E.M., Blandini, F.

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Determination of Ambroxol Levels in Plasma and Cerebrospinal Fluid by Online Solid-Phase Extraction Coupled with Liquid Chromatography-Tandem Mass Spectrometry in GBA-Parkinson Dis... von Franco, V., Palmisani, M., Colucci, F., De Micco, R., Aloisio, S., Cazzaniga, F., Cerri, S., Cuconato, G., Devigili, G., Franciotta, D., Eleopra, R., Elia, A., Garavaglia, B., Andreasi, N. Golfrè, Invernizzi, F., Leta, V., Moda, F., Mitrotti, P., Picascia, M., Reale, C., Romito, L., Siciliano, M., Stiuso, R., Tessitore, A., Valente, E.M., Avenali, M., Cilia, R.

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Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations von Sanna-Cherchi, Simone, Khan, Kamal, Westland, Rik, Krithivasan, Priya, Fievet, Lorraine, Rasouly, Hila Milo, Ionita-Laza, Iuliana, Capone, Valentina P., Fasel, David A., Kiryluk, Krzysztof, Kamalakaran, Sitharthan, Bodria, Monica, Otto, Edgar A., Sampson, Matthew G., Gillies, Christopher E., Vega-Warner, Virginia, Vukojevic, Katarina, Pediaditakis, Igor, Makar, Gabriel S., Mitrotti, Adele, Verbitsky, Miguel, Martino, Jeremiah, Liu, Qingxue, Na, Young-Ji, Goj, Vinicio, Ardissino, Gianluigi, Gigante, Maddalena, Gesualdo, Loreto, Janezcko, Magdalena, Zaniew, Marcin, Mendelsohn, Cathy Lee, Shril, Shirlee, Hildebrandt, Friedhelm, van Wijk, Joanna A.E., Arapovic, Adela, Saraga, Marijan, Allegri, Landino, Izzi, Claudia, Scolari, Francesco, Tasic, Velibor, Ghiggeri, Gian Marco, Latos-Bielenska, Anna, Materna-Kiryluk, Anna, Mane, Shrikant, Goldstein, David B., Lifton, Richard P., Katsanis, Nicholas, Davis, Erica E., Gharavi, Ali G.

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Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations von Sanna-Cherchi, Simone, Khan, Kamal, Westland, Rik, Krithivasan, Priya, Fievet, Lorraine, Rasouly, Hila Milo, Ionita-Laza, Iuliana, Capone, Valentina P., Fasel, David A., Kiryluk, Krzysztof, Kamalakaran, Sitharthan, Bodria, Monica, Otto, Edgar A., Sampson, Matthew G., Gillies, Christopher E., Vega-Warner, Virginia, Vukojevic, Katarina, Pediaditakis, Igor, Makar, Gabriel S., Mitrotti, Adele, Verbitsky, Miguel, Martino, Jeremiah, Liu, Qingxue, Na, Young-Ji, Goj, Vinicio, Ardissino, Gianluigi, Gigante, Maddalena, Gesualdo, Loreto, Janezcko, Magdalena, Zaniew, Marcin, Mendelsohn, Cathy Lee, Shril, Shirlee, Hildebrandt, Friedhelm, van Wijk, Joanna A.E., Arapovic, Adela, Saraga, Marijan, Allegri, Landino, Izzi, Claudia, Scolari, Francesco, Tasic, Velibor, Ghiggeri, Gian Marco, Latos-Bielenska, Anna, Materna-Kiryluk, Anna, Mane, Shrikant, Goldstein, David B., Lifton, Richard P., Katsanis, Nicholas, Davis, Erica E., Gharavi, Ali G.

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Retrospective Study On Recurrent Glomerulonephritis (RGN) in The Transplanted Kidney: Our Case Study: Abstract# B948 von Argentiero, L., Schena, A., Rossini, M., Manno, C., Martino, M., Mitrotti, A., Giliberti, M., Digiorgio, C., Dipalma, A., Ditonno, P., Battaglia, M., Grandaliano, G., Gesualdo, L.

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