The flavor test is a sensitive tool in identifying the flavor sensorineural dysfunction in Parkinson’s disease von De Rosa, Anna, Nettore, Immacolata Cristina, Cantone, Elena, Maione, Luigi, Desiderio, Silvio, Peluso, Silvio, Saccà, Francesco, Manganelli, Fiore, Bruzzese, Dario, Colao, Annamaria, De Michele, Giuseppe, Macchia, Paolo Emidio

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Searching for Potential Lipid Biomarkers of Parkinson's Disease in Parkin-Mutant Human Skin Fibroblasts by HILIC-ESI-MS/MS: Preliminary Findings von Calvano, Cosima D, Ventura, Giovanni, Sardanelli, Anna Maria M, Savino, Laura, Losito, Ilario, Michele, Giuseppe De, Palmisano, Francesco, Cataldi, Tommaso R I

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Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa von Ibáñez, Pablo, Lesage, Suzanne, Lohmann, Ebba, Thobois, Stéphane, Michele, Giuseppe De, Borg, Michel, Agid, Yves, Dürr, Alexandra, Brice, Alexis

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Reversible Valproate-Induced Subacute Encephalopathy Associated With a MT-ATP8 Variant in the Mitochondrial Genome von De Michele, Giovanna, Sorrentino, Pierpaolo, Nesti, Claudia, Rubegni, Anna, Ruggiero, Lucia, Peluso, Silvio, Antenora, Antonella, Quarantelli, Mario, Filla, Alessandro, De Michele, Giuseppe, Santorelli, Filippo M

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Spinocerebellar ataxia type 48: last but not least von De Michele, Giuseppe, Santorelli, Filippo

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The heterogeneity of early Parkinson's disease: a cluster analysis on newly diagnosed untreated patients von Erro, Roberto, Vitale, Carmine, Amboni, Marianna, Picillo, Marina, Moccia, Marcello, Longo, Katia, Santangelo, Gabriella, De Rosa, Anna, Allocca, Roberto, Giordano, Flavio, Orefice, Giuseppe, De Michele, Giuseppe, Santoro, Lucio, Pellecchia, Maria Teresa, Barone, Paolo

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Cutaneous sensory and autonomic denervation in progressive supranuclear palsy von Dubbioso, Raffaele, Provitera, Vincenzo, Vitale, Floriana, Stancanelli, Annamaria, Borreca, Ilaria, Caporaso, Giuseppe, De Michele, Giovanna, De Rosa, Anna, Picillo, Marina, Barone, Paolo, Iodice, Rosa, Manganelli, Fiore, De Michele, Giuseppe, Santoro, Lucio, Nolano, Maria

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Spectral Domain and Angiography Optical Coherence Tomography in Parkinson’s Disease: Structural And Vascular Changes in the Retina Correlate with Disease Severity and Progression von Di Maio, Laura Giovanna, Cennamo, Gilda, Montorio, Daniela, De Michele, Giovanna, Palmieri, Gianluigi Rosario, Baratto, Luigi, Perillo, Sandra, Giglio, Augusta, Filla, Alessandro, Brescia Morra, Vincenzo, De Michele, Giuseppe, Costagliola, Ciro, De Rosa, Anna

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Degenerative and acquired sporadic adult onset ataxia von Lieto, Maria, Roca, Alessandro, Santorelli, Filippo Maria, Fico, Tommasina, De Michele, Giovanna, Bellofatto, Marta, Saccà, Francesco, De Michele, Giuseppe, Filla, Alessandro

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International Guidelines for the Treatment of Huntington's Disease von Bachoud-Lévi, Anne-Catherine, Ferreira, Joaquim, Massart, Renaud, Youssov, Katia, Rosser, Anne, Busse, Monica, Craufurd, David, Reilmann, Ralf, De Michele, Giuseppe, Rae, Daniela, Squitieri, Ferdinando, Seppi, Klaus, Perrine, Charles, Scherer-Gagou, Clarisse, Audrey, Olivier, Verny, Christophe, Burgunder, Jean-Marc

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Spinocerebellar ataxia type 48: last but not least von De Michele, Giovanna, Galatolo, Daniele, Barghigiani, Melissa, Dello Iacovo, Diletta, Trovato, Rosanna, Tessa, Alessandra, Salvatore, Elena, Filla, Alessandro, De Michele, Giuseppe, Santorelli, Filippo M.

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Mutations in the SPAST gene causing hereditary spastic paraplegia are related to global topological alterations in brain functional networks von Rucco, Rosaria, Liparoti, Marianna, Jacini, Francesca, Baselice, Fabio, Antenora, Antonella, De Michele, Giuseppe, Criscuolo, Chiara, Vettoliere, Antonio, Mandolesi, Laura, Sorrentino, Giuseppe, Sorrentino, Pierpaolo

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DNA damage signatures in peripheral blood cells as biomarkers in prodromal huntington disease von Castaldo, Imma, De Rosa, Mariarosaria, Romano, Antonella, Zuchegna, Candida, Squitieri, Ferdinando, Mechelli, Rosella, Peluso, Silvio, Borrelli, Cristiana, Del Mondo, Angelo, Salvatore, Elena, Vescovi, Luigi Angelo, Migliore, Simone, De Michele, Giuseppe, Ristori, Giovanni, Romano, Silvia, Avvedimento, Enrico Vittorio, Porcellini, Antonio

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Alteration of endosomal trafficking is associated with early-onset parkinsonism caused by SYNJ1 mutations von Fasano, Dominga, Parisi, Silvia, Pierantoni, Giovanna Maria, De Rosa, Anna, Picillo, Marina, Amodio, Giuseppina, Pellecchia, Maria Teresa, Barone, Paolo, Moltedo, Ornella, Bonifati, Vincenzo, De Michele, Giuseppe, Nitsch, Lucio, Remondelli, Paolo, Criscuolo, Chiara, Paladino, Simona

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Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy von Caporali, Leonardo, Iommarini, Luisa, La Morgia, Chiara, Olivieri, Anna, Achilli, Alessandro, Maresca, Alessandra, Valentino, Maria Lucia, Capristo, Mariantonietta, Tagliavini, Francesca, Del Dotto, Valentina, Zanna, Claudia, Liguori, Rocco, Barboni, Piero, Carbonelli, Michele, Cocetta, Veronica, Montopoli, Monica, Martinuzzi, Andrea, Cenacchi, Giovanna, De Michele, Giuseppe, Testa, Francesco, Nesti, Anna, Simonelli, Francesca, Porcelli, Anna Maria, Torroni, Antonio, Carelli, Valerio

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Episodic ataxia and severe infantile phenotype in spinocerebellar ataxia type 14: expansion of the phenotype and novel mutations von De Michele, Giovanna, Galatolo, Daniele, Galosi, Serena, Mignarri, Andrea, Silvestri, Gabriella, Casali, Carlo, Leuzzi, Vincenzo, Ricca, Ivana, Barghigiani, Melissa, Tessa, Alessandra, Cioffi, Ettore, Caputi, Caterina, Riso, Vittorio, Dotti, Maria Teresa, Saccà, Francesco, De Michele, Giuseppe, Cocozza, Sirio, Filla, Alessandro, Santorelli, Filippo M.

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Othello syndrome in Parkinson’s disease: a systematic review and report of a case series von De Michele, Giovanna, Palmieri, Gianluigi Rosario, Pane, Chiara, Dello Iacovo, Carmen Diletta Paola, Perillo, Sandra, Saccà, Francesco, De Michele, Giuseppe, De Rosa, Anna

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PARK20 caused by SYNJ1 homozygous Arg258Gln mutation in a new Italian family von Olgiati, Simone, De Rosa, Anna, Quadri, Marialuisa, Criscuolo, Chiara, Breedveld, Guido J., Picillo, Marina, Pappatà, Sabina, Quarantelli, Mario, Barone, Paolo, De Michele, Giuseppe, Bonifati, Vincenzo

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Optical coherence tomography angiography findings in Huntington’s disease von Di Maio, Laura Giovanna, Montorio, Daniela, Peluso, Silvio, Dolce, Pasquale, Salvatore, Elena, De Michele, Giuseppe, Cennamo, Gilda

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Primary familial brain calcification caused by a novel homozygous MYORG mutation in a consanguineous Italian family von Ramos, Eliana Marisa, Roca, Alessandro, Chumchim, Noravit, Dokuru, Deepika Reddy, Van Berlo, Victoria, De Michele, Giovanna, Lieto, Maria, Tedeschi, Enrico, De Michele, Giuseppe, Coppola, Giovanni

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