Metachromatic leukodystrophy with late adult-onset: diagnostic clues and differences from other genetic leukoencephalopathies with dementia von Benzoni, Chiara, Moscatelli, Marco, Fenu, Silvia, Venerando, Anna, Salsano, Ettore

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A systematic review and meta-analysis of GFAP gene variants in Alexander disease von Grossi, Alice, Rosamilia, Francesca, Carestiato, Silvia, Salsano, Ettore, Ceccherini, Isabella, Bachetti, Tiziana

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Correction to: Metachromatic leukodystrophy with late adult-onset: diagnostic clues and differences from other genetic leukoencephalopathies with dementia von Benzoni, Chiara, Moscatelli, Marco, Fenu, Silvia, Venerando, Anna, Salsano, Ettore

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Extensive leukoencephalopathy in coeliac disease: report of three cases and review of the literature von Benzoni, Chiara, Moscatelli, Marco, Fenu, Silvia, Pareyson, Davide, Salsano, Ettore

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Considering the myelin-centric hypothesis: insights from Budka's historical adrenomyeloneuropathy case report von Salsano, Ettore, Benzoni, Chiara

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Peripheral neuropathy in mitochondrial disorders von Pareyson, Davide, Dr, Piscosquito, Giuseppe, MD, Moroni, Isabella, MD, Salsano, Ettore, MD, Zeviani, Massimo, MD

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Adult‐onset leukoencephalopathy caused by CSF1R mutations: Is all that glitters gold? von Salsano, Ettore, Benzoni, Chiara

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Asymptomatic adrenoleukodystrophy in elderly males von Benzoni, Chiara, Fenu, Silvia, Pensato, Viviana, Mauro, Elena, Gellera, Cinzia, Pareyson, Davide, Salsano, Ettore

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Primary brain calcification: an international study reporting novel variants and associated phenotypes von Ramos, Eliana Marisa, Carecchio, Miryam, Lemos, Roberta, Ferreira, Joana, Legati, Andrea, Sears, Renee Louise, Hsu, Sandy Chan, Panteghini, Celeste, Magistrelli, Luca, Salsano, Ettore, Esposito, Silvia, Taroni, Franco, Richard, Anne-Claire, Tranchant, Christine, Anheim, Mathieu, Ayrignac, Xavier, Goizet, Cyril, Vidailhet, Marie, Maltete, David, Wallon, David, Frebourg, Thierry, Pimentel, Lylyan, Geschwind, Daniel H, Vanakker, Olivier, Galasko, Douglas, Fogel, Brent L, Innes, A Micheil, Ross, Alison, Dobyns, William B, Alcantara, Diana, O'Driscoll, Mark, Hannequin, Didier, Campion, Dominique, Oliveira, João R, Garavaglia, Barbara, Coppola, Giovanni, Nicolas, Gaël

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Hypomyelinating leukodystrophies in adults: Clinical and genetic features von Di Bella, Daniela, Magri, Stefania, Benzoni, Chiara, Farina, Laura, Maccagnano, Carmelo, Sarto, Elisa, Moscatelli, Marco, Baratta, Silvia, Ciano, Claudia, Piacentini, Sylvie H. M. J., Draghi, Lara, Mauro, Elena, Pareyson, Davide, Gellera, Cinzia, Taroni, Franco, Salsano, Ettore

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Magnetic Resonance Imaging Alteration of the Brain in a Patient With Coronavirus Disease 2019 (COVID-19) and Anosmia von Politi, Letterio S, Salsano, Ettore, Grimaldi, Marco

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Neuro-telehealth for fragile patients in a tertiary referral neurological institute during the COVID-19 pandemic in Milan, Lombardy von Pareyson, Davide, Pantaleoni, Chiara, Eleopra, Roberto, De Filippis, Giuseppe, Moroni, Isabella, Freri, Elena, Zibordi, Federica, Bulgheroni, Sara, Pagliano, Emanuela, Sarti, Daniela, Silvani, Antonio, Grazzi, Licia, Tiraboschi, Pietro, Didato, Giuseppe, Anghileri, Elena, Bersano, Anna, Valentini, Laura, Piacentini, Sylvie, Muscio, Cristina, Leonardi, Matilde, Mariotti, Caterina, Eoli, Marica, Nuzzo, Sara, Tagliavini, Fabrizio, Confalonieri, Paolo, De Giorgi, Francesca

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Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations von Orthmann-Murphy, Jennifer L., Salsano, Ettore, Abrams, Charles K., Bizzi, Alberto, Uziel, Graziella, Freidin, Mona M., Lamantea, Eleonora, Zeviani, Massimo, Scherer, Steven S., Pareyson, Davide

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Novel deep intronic mutation in PLA2G6 causing early-onset Parkinson’s disease with brain iron accumulation through pseudo-exon activation von Cavestro, Chiara, Panteghini, Celeste, Reale, Chiara, Nasca, Alessia, Fenu, Silvia, Salsano, Ettore, Chiapparini, Luisa, Garavaglia, Barbara, Pareyson, Davide, Di Meo, Ivano, Tiranti, Valeria

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Optical coherence tomography in adult adrenoleukodystrophy: a cross-sectional and longitudinal study von Bianchi-Marzoli, Stefania, Fenu, Silvia, Melzi, Lisa, Benzoni, Chiara, Antonazzo, Filippo, Tomas Roldan, Eugenia, Farina, Laura, Tremolada, Gemma, Mauro, Elena, Pensato, Viviana, Gellera, Cinzia, Pareyson, Davide, Salsano, Ettore

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Interval between contrast administration and T1-weighted MRI for cerebral adrenoleukodystrophy: a single-case observation von Moscatelli, Marco, Benzoni, Chiara, Doniselli, Fabio M., Verri, Mattia, Pascuzzo, Riccardo, Aquino, Domenico, Mazzi, Federica, Erbetta, Alessandra, Salsano, Ettore

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Early-onset progressive spastic paraplegia caused by a novel TUBB4A mutation: brain MRI and FDG-PET findings von Sagnelli, Anna, Magri, Stefania, Farina, Laura, Chiapparini, Luisa, Marotta, Giorgio, Tonduti, Davide, Consonni, Monica, Scigliuolo, Graziana Maria, Benti, Riccardo, Pareyson, Davide, Taroni, Franco, Salsano, Ettore, Di Bella, Daniela

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Human adipose-derived mesenchymal stem cells as a new model of spinal and bulbar muscular atrophy von Dossena, Marta, Bedini, Gloria, Rusmini, Paola, Giorgetti, Elisa, Canazza, Alessandra, Tosetti, Valentina, Salsano, Ettore, Sagnelli, Anna, Mariotti, Caterina, Gellera, Cinzia, Navone, Stefania Elena, Marfia, Giovanni, Alessandri, Giulio, Corsi, Fabio, Parati, Eugenio Agostino, Pareyson, Davide, Poletti, Angelo

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X-linked Charcot-Marie-Tooth type 1: stroke-like presentation of a novel GJB1 mutation von Sagnelli, Anna, Piscosquito, Giuseppe, Chiapparini, Luisa, Ciano, Claudia, Salsano, Ettore, Saveri, Paola, Milani, Micaela, Taroni, Franco, Pareyson, Davide

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Leukodystrophy or genetic leukoencephalopathy? Nature does not make leaps von Salsano, Ettore

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