Multimodal MRI Longitudinal Assessment of White and Gray Matter in Different SPG Types of Hereditary Spastic Paraparesis by Montanaro, Domenico, Vavla, M., Frijia, F., Aghakhanyan, G., Baratto, A., Coi, A., Stefan, C., Girardi, G., Paparella, G., De Cori, S., Totaro, P., Lombardo, F., Piccoli, G., Martinuzzi, Andrea

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Brain white matter involvement in hereditary spastic paraplegias: analysis with multiple diffusion tensor indices by Aghakhanyan, G, Martinuzzi, A, Frijia, F, Vavla, M, Hlavata, H, Baratto, A, Martino, N, Paparella, G, Montanaro, D

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Looking for a sensitive biomarker for genetically determined neurodegenerative diseases through the window of the eye by Martinuzzi, A., Vavla, M., Capello, G., Papayannis, A., Petacchi, E., Paparella, G., Privato, F., Prosdocimo, G.

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Extraocular phenotyping of mitochondrial optic neuropathy by Martinuzzi, A., Vavla, M., Papayannis, A., Petacchi, E., Carraro, E., Paparella, G., Privato, F., Prosdocimo, G.

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A novel mitofusin 2 MFN2 gene mutation causing early onset Charcot-Marie-Tooth 2A disease: Genetic, clinical and MR spectroscopy characterization by Vavla, M, Montanaro, D, Frijia, F, Aghakhanyan, G, Mostacciuolo, M.L, Carraro, E, Casanova, V

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Brain Structure and Degeneration Staging in Friedreich Ataxia: Magnetic Resonance Imaging Volumetrics from the ENIGMA‐Ataxia Working Group by Harding, Ian H., Chopra, Sidhant, Arrigoni, Filippo, Boesch, Sylvia, Brunetti, Arturo, Cocozza, Sirio, Corben, Louise A., Deistung, Andreas, Delatycki, Martin, Diciotti, Stefano, Dogan, Imis, Evangelisti, Stefania, França, Marcondes C., Göricke, Sophia L., Georgiou‐Karistianis, Nellie, Gramegna, Laura L., Henry, Pierre‐Gilles, Hernandez‐Castillo, Carlos R., Hutter, Diane, Jahanshad, Neda, Joers, James M., Lenglet, Christophe, Lodi, Raffaele, Manners, David N., Martinez, Alberto R. M., Martinuzzi, Andrea, Marzi, Chiara, Mascalchi, Mario, Nachbauer, Wolfgang, Pane, Chiara, Peruzzo, Denis, Pisharady, Pramod K., Pontillo, Giuseppe, Reetz, Kathrin, Rezende, Thiago J. R., Romanzetti, Sandro, Saccà, Francesco, Scherfler, Christoph, Schulz, Jörg B., Stefani, Ambra, Testa, Claudia, Thomopoulos, Sophia I., Timmann, Dagmar, Tirelli, Stefania, Tonon, Caterina, Vavla, Marinela, Egan, Gary F., Thompson, Paul M.

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Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry) by Pinós, Tomàs, Andreu, Antoni L, Bruno, Claudio, Hadjigeorgiou, Georgios M, Haller, Ronald G, Laforêt, Pascal, Lucía, Alejandro, Martín, Miguel A, Martinuzzi, Andrea, Navarro, Carmen, Oflazer, Piraye, Pouget, Jean, Quinlivan, Ros, Sacconi, Sabrina, Scalco, Renata S, Toscano, Antonio, Vissing, John, Vorgerd, Matthias, Wakelin, Andrew, Martí, Ramon

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