GBA , Gaucher Disease, and Parkinson's Disease: From Genetic to Clinic to New Therapeutic Approaches von Riboldi, Giulietta M, Di Fonzo, Alessio B

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Adaptive deep brain stimulation controls levodopa‐induced side effects in Parkinsonian patients von Rosa, Manuela, Arlotti, Mattia, Marceglia, Sara, Cogiamanian, Filippo, Ardolino, Gianluca, Fonzo, Alessio Di, Lopiano, Leonardo, Scelzo, Emma, Merola, Aristide, Locatelli, Marco, Rampini, Paolo M., Priori, Alberto

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The unexpected finding of CNS autoantibodies in GBA1 mutation carriers with atypical parkinsonism von Di Biasio, Francesca, Lazzeri, Giulia, Monfrini, Edoardo, Mandich, Paola, Trevisan, Lucia, Morbelli, Silvia, Markushi, Tiziana Benzi, Avanzino, Laura, Di Fonzo, Alessio

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Soft cerebellar signs unveil RARS2‐related epilepsy von Yahya, Vidal, Dilena, Robertino, Del Bo, Roberto, Magni, Manuela, Biella, Fabio, Salani, Sabrina, Fortunato, Francesco, Scola, Elisa, Di Fonzo, Alessio, Monfrini, Edoardo

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Mutations in DNA2 Link Progressive Myopathy to Mitochondrial DNA Instability von Ronchi, Dario, Di Fonzo, Alessio, Lin, Weiqiang, Bordoni, Andreina, Liu, Changwei, Fassone, Elisa, Pagliarani, Serena, Rizzuti, Mafalda, Zheng, Li, Filosto, Massimiliano, Ferrò, Maria Teresa, Ranieri, Michela, Magri, Francesca, Peverelli, Lorenzo, Li, Hongzhi, Yuan, Yate-Ching, Corti, Stefania, Sciacco, Monica, Moggio, Maurizio, Bresolin, Nereo, Shen, Binghui, Comi, Giacomo Pietro

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GABRB1‐related early onset developmental and epileptic encephalopathy: Clinical trajectory and novel de novo mutation von Monfrini, Edoardo, Borellini, Linda, Zirone, Eleonora, Yahya, Vidal, Mauri, Eleonora, Molisso, Maria Takeko, Mameli, Francesca, Ruggiero, Fabiana, Comi, Giacomo Pietro, Barbieri, Sergio, Di Fonzo, Alessio, Dilena, Robertino

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Nuclear Pore Complex Dysfunction in Dystonia Pathogenesis: Nucleoporins in the Spotlight von Di Fonzo, Alessio, Zech, Michael

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The Role of Mitochondria in Neurodegenerative Diseases: the Lesson from Alzheimer’s Disease and Parkinson’s Disease von Monzio Compagnoni, Giacomo, Di Fonzo, Alessio, Corti, Stefania, Comi, Giacomo P., Bresolin, Nereo, Masliah, Eliezer

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Editorial: Genetic advances and translational applications in movement disorders von Riboldi, Giulietta M., Di Fonzo, Alessio B., Stephen, Christopher D.

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Nucleo-cytoplasmic transport defects and protein aggregates in neurodegeneration von Bitetto, Giacomo, Di Fonzo, Alessio

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Genetic Evidence for Endolysosomal Dysfunction in Parkinson's Disease: A Critical Overview von Yahya, Vidal, Di Fonzo, Alessio, Monfrini, Edoardo

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Comprehensive Genomic Analysis Reveals the Prognostic Role of LRRK2 Copy-Number Variations in Human Malignancies von Lopez, Gianluca, Lazzeri, Giulia, Rappa, Alessandra, Isimbaldi, Giuseppe, Cribiù, Fulvia Milena, Guerini-Rocco, Elena, Ferrero, Stefano, Vaira, Valentina, Di Fonzo, Alessio

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Understanding the pathogenesis of multiple system atrophy: state of the art and future perspectives von Monzio Compagnoni, Giacomo, Di Fonzo, Alessio

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The Length of SNCA Rep1 Microsatellite May Influence Cognitive Evolution in Parkinson's Disease von Corrado, Lucia, De Marchi, Fabiola, Tunesi, Sara, Oggioni, Gaia Donata, Carecchio, Miryam, Magistrelli, Luca, Tesei, Silvana, Riboldazzi, Giulio, Di Fonzo, Alessio, Locci, Clarissa, Trezzi, Ilaria, Zangaglia, Roberta, Cereda, Cristina, D'Alfonso, Sandra, Magnani, Corrado, Comi, Giacomo P, Bono, Giorgio, Pacchetti, Claudio, Cantello, Roberto, Goldwurm, Stefano, Comi, Cristoforo

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In vitro models of multiple system atrophy from primary cells to induced pluripotent stem cells von Abati, Elena, Di Fonzo, Alessio, Corti, Stefania

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Reply to: “Lack of Association between TWNK Rare Variants and Parkinson's Disease in a Chinese Cohort” von Percetti, Marco, Monfrini, Edoardo, Caporali, Leonardo, Minardi, Raffaella, Carelli, Valerio, Valente, Enza Maria, Di Fonzo, Alessio

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Genetics of Movement Disorders and the Practicing Clinician; Who and What to Test for? von Di Fonzo, Alessio, Monfrini, Edoardo, Erro, Roberto

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Reply to: No Association between Rare TWNK Variants and Parkinson's Disease in European Cohorts von Percetti, Marco, Monfrini, Edoardo, Caporali, Leonardo, Minardi, Raffaella, Carelli, Valerio, Valente, Enza Maria, Di Fonzo, Alessio

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Freezing of gait: overview on etiology, treatment, and future directions von Falla, Marika, Cossu, Giovanni, Di Fonzo, Alessio

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Chorea‐Acanthocytosis Presenting with Parkinsonism‐Dystonia without Chorea von Monfrini, Edoardo, Di Fonzo, Alessio, Morgante, Francesca

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