Antiphospholipid-Related Chorea

por Peluso, Silvio, Antenora, Antonella, De Rosa, Anna, Roca, Alessandro, Maddaluno, Gennaro, Morra, Vincenzo Brescia, De Michele, Giuseppe
Publicado 2012

The Multiple Faces of Spinocerebellar Ataxia type 2

por Antenora, Antonella, Rinaldi, Carlo, Roca, Alessandro, Pane, Chiara, Lieto, Maria, Saccà, Francesco, Peluso, Silvio, De Michele, Giuseppe, Filla, Alessandro
Publicado 2017

Searching for Potential Lipid Biomarkers of Parkinson’s Disease in Parkin-Mutant Human Skin Fibroblasts by HILIC-ESI-MS/MS: Preliminary Findings

por Calvano, Cosima D., Ventura, Giovanni, Sardanelli, Anna Maria M., Savino, Laura, Losito, Ilario, De Michele, Giuseppe, Palmisano, Francesco, Cataldi, Tommaso R. I.
Publicado 2019

Mutations in the SPAST gene causing hereditary spastic paraplegia are related to global topological alterations in brain functional networks

por Rucco, Rosaria, Liparoti, Marianna, Jacini, Francesca, Baselice, Fabio, Antenora, Antonella, De Michele, Giuseppe, Criscuolo, Chiara, Vettoliere, Antonio, Mandolesi, Laura, Sorrentino, Giuseppe, Sorrentino, Pierpaolo
Publicado 2019

Othello syndrome in Parkinson’s disease: a systematic review and report of a case series

por De Michele, Giovanna, Palmieri, Gianluigi Rosario, Pane, Chiara, Dello Iacovo, Carmen Diletta Paola, Perillo, Sandra, Saccà, Francesco, De Michele, Giuseppe, De Rosa, Anna
Publicado 2021

Default-Mode Network Changes in Huntington’s Disease: An Integrated MRI Study of Functional Connectivity and Morphometry

por Quarantelli, Mario, Salvatore, Elena, Giorgio, Sara Maria Delle Acque, Filla, Alessandro, Cervo, Amedeo, Russo, Cinzia Valeria, Cocozza, Sirio, Massarelli, Marco, Brunetti, Arturo, De Michele, Giuseppe
Publicado 2013

Stability of erythropoietin repackaging in polypropylene syringes for clinical use

por Marsili, Angela, Puorro, Giorgia, Pane, Chiara, de Rosa, Anna, Defazio, Giovanni, Casali, Carlo, Cittadini, Antonio, de Michele, Giuseppe, Florio, Brunello Ettore, Filla, Alessandro, Saccà, Francesco
Publicado 2017

Reversible Valproate-Induced Subacute Encephalopathy Associated With a MT-ATP8 Variant in the Mitochondrial Genome

por 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.
Publicado 2018

A Combined Nucleic Acid and Protein Analysis in Friedreich Ataxia: Implications for Diagnosis, Pathogenesis and Clinical Trial Design

por Saccà, Francesco, Puorro, Giorgia, Antenora, Antonella, Marsili, Angela, Denaro, Alessandra, Piro, Raffaele, Sorrentino, Pierpaolo, Pane, Chiara, Tessa, Alessandra, Brescia Morra, Vincenzo, Cocozza, Sergio, De Michele, Giuseppe, Santorelli, Filippo M., Filla, Alessandro
Publicado 2011

Autonomic disorders and myocardial 123I-metaiodobenzylguanidine scintigraphy in Huntington’s disease

por Assante, Roberta, Salvatore, Elena, Nappi, Carmela, Peluso, Silvio, De Simini, Giovanni, Di Maio, Luigi, Palmieri, Gianluigi Rosario, Ferrara, Isabella Pia, Roca, Alessandro, De Michele, Giuseppe, Cuocolo, Alberto, Pappatà, Sabina, De Rosa, Anna
Publicado 2020

A new genetic cause of spastic ataxia: the p.Glu415Lys variant in TUBA4A

por Torella, Annalaura, Ricca, Ivana, Piluso, Giulio, Galatolo, Daniele, De Michele, Giuseppe, Zanobio, Mariateresa, Trovato, Rosanna, De Michele, Giovanna, Zeuli, Roberta, Pane, Chiara, Cocozza, Sirio, Saccà, Francesco, Santorelli, Filippo M., Nigro, Vincenzo, Filla, Alessandro
Publicado 2023

The Heterogeneity of Early Parkinson’s Disease: A Cluster Analysis on Newly Diagnosed Untreated Patients

por 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
Publicado 2013

Alteration of endosomal trafficking is associated with early-onset parkinsonism caused by SYNJ1 mutations

por 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
Publicado 2018

International Guidelines for the Treatment of Huntington's Disease

por 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
Publicado 2019

Episodic ataxia and severe infantile phenotype in spinocerebellar ataxia type 14: expansion of the phenotype and novel mutations

por 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.
Publicado 2021

PERK-Mediated Unfolded Protein Response Activation and Oxidative Stress in PARK20 Fibroblasts

por Amodio, Giuseppina, Moltedo, Ornella, Fasano, Dominga, Zerillo, Lucrezia, Oliveti, Marco, Di Pietro, Paola, Faraonio, Raffaella, Barone, Paolo, Pellecchia, Maria Teresa, De Rosa, Anna, De Michele, Giuseppe, Polishchuk, Elena, Polishchuk, Roman, Bonifati, Vincenzo, Nitsch, Lucio, Pierantoni, Giovanna Maria, Renna, Maurizio, Criscuolo, Chiara, Paladino, Simona, Remondelli, Paolo
Publicado 2019

Coverage of the requirements of first and second level stroke unit in Italy

por Bandettini di Poggio, Monica, Toni, Danilo, Gandolfo, Carlo, Paolicelli, Damiano, Zini, Andrea, Agostoni, Elio, Bandini, Fabio, Ragno, Michele, Altavista, Maria Concetta, Bertolotto, Antonio, Siciliano, Gabriele, Vecchio, Michele, Tambasco, Nicola, Gambardella, Antonio, Manganotti, Paolo, Melis, Maurizio, Onofrj, Marco, De Michele, Giuseppe, Reale, Nicoletta, Tedeschi, Gioacchino, Mancardi, GianLuigi
Publicado 2020

Neuroacanthocytosis Syndromes in an Italian Cohort: Clinical Spectrum, High Genetic Variability and Muscle Involvement

por Vaisfeld, Alessandro, Bruno, Giorgia, Petracca, Martina, Bentivoglio, Anna Rita, Servidei, Serenella, Vita, Maria Gabriella, Bove, Francesco, Straccia, Giulia, Dato, Clemente, Di Iorio, Giuseppe, Sampaolo, Simone, Peluso, Silvio, De Rosa, Anna, De Michele, Giuseppe, Barghigiani, Melissa, Galatolo, Daniele, Tessa, Alessandra, Santorelli, Filippo, Chiurazzi, Pietro, Melone, Mariarosa Anna Beatrice
Publicado 2021

PDCD10 Gene Mutations in Multiple Cerebral Cavernous Malformations

por Cigoli, Maria Sole, Avemaria, Francesca, De Benedetti, Stefano, Gesu, Giovanni P., Accorsi, Lucio Giordano, Parmigiani, Stefano, Corona, Maria Franca, Capra, Valeria, Mosca, Andrea, Giovannini, Simona, Notturno, Francesca, Ciccocioppo, Fausta, Volpi, Lilia, Estienne, Margherita, De Michele, Giuseppe, Antenora, Antonella, Bilo, Leda, Tavoni, Antonietta, Zamponi, Nelia, Alfei, Enrico, Baranello, Giovanni, Riva, Daria, Penco, Silvana
Publicado 2014

Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber’s hereditary optic neuropathy

por 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
Publicado 2018