Altered apoptosis regulation in Kufor–Rakeb syndrome patients with mutations in the ATP13A2 gene

by Radi, Elena, Formichi, Patrizia, Maio, Giuseppe Di, Battisti, Carla, Federico, Antonio
Published 2012

Cerebrolysin administration reduces oxidative stress-induced apoptosis in limphocytes from healthy individuals

by Formichi, Patrizia, Radi, Elena, Battisti, Carla, Di Maio, Giuseppe, Muresanu, Dafin, Federico, Antonio
Published 2012

Functional and Brain Activation Changes Following Specialized Upper-Limb Exercise in Parkinson’s Disease

by Messa, Luca Valerio, Ginanneschi, Federica, Momi, Davide, Monti, Lucia, Battisti, Carla, Cioncoloni, David, Pucci, Barbara, Santarnecchi, Emiliano, Rossi, Alessandro
Published in Front Hum Neurosci (2019)

Neurophthalmologic and Orthoptic Ambulatory Assessments Reveal Ocular and Visual Changes in Patients With Early Alzheimer and Parkinson's Disease

by Bargagli, Alessia, Fontanelli, Enrica, Zanca, Dario, Castelli, Ilaria, Rosini, Francesca, Maddii, Silvia, Di Donato, Ilaria, Carluccio, Alessandra, Battisti, Carla, Tosi, Gian M., Dotti, Maria T., Rufa, Alessandra
Published in Front Neurol (2020)

Heterozygous mutations of HTRA1 gene in patients with familial cerebral small vessel disease

by Di Donato, Ilaria, Bianchi, Silvia, Gallus, Gian Nicola, Cerase, Alfonso, Taglia, Ilaria, Pescini, Francesca, Nannucci, Serena, Battisti, Carla, Inzitari, Domenico, Pantoni, Leonardo, Zini, Andrea, Federico, Antonio, Dotti, Maria Teresa
Published in CNS Neurosci Ther (2017)

Prevalence and impact of COVID-19 in Parkinson’s disease: evidence from a multi-center survey in Tuscany region

by Del Prete, Eleonora, Francesconi, Alessio, Palermo, Giovanni, Mazzucchi, Sonia, Frosini, Daniela, Morganti, Riccardo, Coleschi, Piero, Raglione, Laura Maria, Vanni, Paola, Ramat, Silvia, Novelli, Alessio, Napolitano, Alessandro, Battisti, Carla, Giuntini, Martina, Rossi, Carlo, Menichetti, Chiara, Ulivelli, Monica, De Franco, Valentino, Rossi, Simone, Bonuccelli, Ubaldo, Ceravolo, Roberto
Published in J Neurol (2020)

Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease

by Quadri, Marialuisa, Federico, Antonio, Zhao, Tianna, Breedveld, Guido J., Battisti, Carla, Delnooz, Cathérine, Severijnen, Lies-Anne, Di Toro Mammarella, Lara, Mignarri, Andrea, Monti, Lucia, Sanna, Antioco, Lu, Peng, Punzo, Francesca, Cossu, Giovanni, Willemsen, Rob, Rasi, Fabrizio, Oostra, Ben A., van de Warrenburg, Bart P., Bonifati, Vincenzo
Published 2012

Next-generation sequencing approach to hyperCKemia: A 2-year cohort study

by Rubegni, Anna, Malandrini, Alessandro, Dosi, Claudia, Astrea, Guja, Baldacci, Jacopo, Battisti, Carla, Bertocci, Giulia, Donati, M. Alice, Dotti, M. Teresa, Federico, Antonio, Giannini, Fabio, Grosso, Salvatore, Guerrini, Renzo, Lenzi, Sara, Maioli, Maria A., Melani, Federico, Mercuri, Eugenio, Sacchini, Michele, Salvatore, Simona, Siciliano, Gabriele, Tolomeo, Deborah, Tonin, Paola, Volpi, Nila, Santorelli, Filippo M., Cassandrini, Denise
Published in Neurol Genet (2019)

Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study

by Astrea, Guja, Romano, Alessandro, Angelini, Corrado, Antozzi, Carlo Giuseppe, Barresi, Rita, Battini, Roberta, Battisti, Carla, Bertini, Enrico, Bruno, Claudio, Cassandrini, Denise, Fanin, Marina, Fattori, Fabiana, Fiorillo, Chiara, Guerrini, Renzo, Maggi, Lorenzo, Mercuri, Eugenio, Morani, Federica, Mora, Marina, Moro, Francesca, Pezzini, Ilaria, Picillo, Esther, Pinelli, Michele, Politano, Luisa, Rubegni, Anna, Sanseverino, Walter, Savarese, Marco, Striano, Pasquale, Torella, Annalaura, Trevisan, Carlo Pietro, Trovato, Rosanna, Zaraieva, Irina, Muntoni, Francesco, Nigro, Vincenzo, D’Amico, Adele, Santorelli, Filippo M.
Published in Orphanet J Rare Dis (2018)

The Spectrum of WRN Mutations in Werner Syndrome Patients

by Huang, Shurong, Lee, Lin, Hanson, Nancy B., Lenaerts, Catherine, Hoehn, Holger, Poot, Martin, Rubin, Craig D., Chen, Da-Fu, Yang, Chih-Chao, Juch, Heike, Dorn, Thomas, Spiegel, Roland, Oral, Elif Arioglu, Abid, Mohammed, Battisti, Carla, Lucci-Cordisco, Emanuela, Neri, Giovanni, Steed, Erin H., Kidd, Alexa, Isley, William, Showalter, David, Vittone, Janet L., Konstantinow, Alexander, Ring, Johannes, Meyer, Peter, Wenger, Sharon L., von Herbay, Axel, Wollina, Uwe, Schuelke, Markus, Huizenga, Carin R., Leistritz, Dru F., Martin, George M., Mian, I. Saira, Oshima, Junko
Published 2006

Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study

by D'Amore, Angelica, Tessa, Alessandra, Casali, Carlo, Dotti, Maria Teresa, Filla, Alessandro, Silvestri, Gabriella, Antenora, Antonella, Astrea, Guja, Barghigiani, Melissa, Battini, Roberta, Battisti, Carla, Bruno, Irene, Cereda, Cristina, Dato, Clemente, Di Iorio, Giuseppe, Donadio, Vincenzo, Felicori, Monica, Fini, Nicola, Fiorillo, Chiara, Gallone, Salvatore, Gemignani, Federica, Gigli, Gian Luigi, Graziano, Claudio, Guerrini, Renzo, Gurrieri, Fiorella, Kariminejad, Ariana, Lieto, Maria, Marques LourenḈo, Charles, Malandrini, Alessandro, Mandich, Paola, Marcotulli, Christian, Mari, Francesco, Massacesi, Luca, Melone, Maria A. B., Mignarri, Andrea, Milone, Roberta, Musumeci, Olimpia, Pegoraro, Elena, Perna, Alessia, Petrucci, Antonio, Pini, Antonella, Pochiero, Francesca, Pons, Maria Roser, Ricca, Ivana, Rossi, Salvatore, Seri, Marco, Stanzial, Franco, Tinelli, Francesca, Toscano, Antonio, Valente, Mariarosaria, Federico, Antonio, Rubegni, Anna, Santorelli, Filippo Maria
Published in Front Neurol (2018)