Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Fabiana Colucci"'
Autor:
Sara Rinaldo, Roberto Cilia, Valentina Leta, Mariarosaria Gammone, Nico Golfrè Andreasi, Fabiana Colucci, Arianna Braccia, Roberta Telese, Marco Fusar Poli, Vincenzo Levi, Luigi Michele Antonio Romito, Francesco Ghilemetti, Elena De Martin, Maria Luisa Fumagalli, Francesca Epifani, Sara Prioni, Paolo Amami, Sylvie Piacentini, Antonio Emanuele Elia, Grazia Devigili, Vittoria Nazzi, Elisa Francesca Maria Ciceri, Mario Stanziano, Marina Grisoli, Valentina Caldiera, Marisa Catotti, Francesco DiMeco, Giacomina Clara Moreschi, Roberto Eleopra
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
MRI-guided focused ultrasound (MRgFUS) lesioning is an innovative, safe and effective treatment which provides an innovative development in the field of minimally invasive stereotactic neurosurgery. Based on the application of focused ultrasound ener
Externí odkaz:
https://doaj.org/article/0bd7201d934244eda114a89272e095c6
Autor:
Matteo Gastaldi, Diego Franciotta, Mario Cirillo, Sara Prioni, Micol Avenali, Fabrizio Esposito, Chiara Reale, Valentina Leta, Enza Maria Valente, Anna Pichiecchio, Barbara Garavaglia, Roberto Eleopra, Marina Grisoli, Roberto Cilia, Luigi Romito, Maria Grazia Bruzzone, Alessandro Tessitore, Ilaria Palmieri, Giada Cuconato, Fabiana Colucci, Pierfrancesco Mitrotti, Rosita De Micco, Marco Fusar Poli, Silvia Cerri, Mario Stanziano, Ana Bacila, Valentina Franco, Cristina Ghezzi, Antonio Emanuele Elia, Grazia Devigili, Nico Golfrè Andreasi, Federico Cazzaniga, Caterina Galandra, Giancarlo Germani, Gerardo Ongari, Marta Picascia, Mattia Verri, Federica Di Nardo, Simone Aloisio, Mattia Siciliano, Paolo Amami, Sylvie Piacentini, Fabio Moda
Publikováno v:
BMJ Neurology Open, Vol 5, Iss 2 (2023)
Background Heterozygous mutations in the GBA gene, encoding the lysosomal enzyme β-glucocerebrosidase (GCase), are the most frequent genetic risk factor for Parkinson’s disease (PD). GBA-related PD (GBA-PD) patients have higher risk of dementia an
Externí odkaz:
https://doaj.org/article/f4439946eac245c38832074e55e2c953
Autor:
Nico Golfrè Andreasi, Vittorio Rispoli, Elena Contaldi, Fabiana Colucci, Lorenzo Mongardi, Michele Alessandro Cavallo, Mariachiara Sensi
Publikováno v:
Brain Stimulation, Vol 13, Iss 2, Pp 280-283 (2020)
Externí odkaz:
https://doaj.org/article/68d5861dc80349dc9d5d50235897b2f2
Publikováno v:
Brain Sciences, Vol 12, Iss 10, p 1308 (2022)
Understanding the pathophysiology and genetic background of Parkinson’s disease (PD) increases the likelihood of developing effective disease-modifying therapeutic strategies. In particular, the discovery of genetic variants causing or increasing t
Externí odkaz:
https://doaj.org/article/76b6457bee2c45baa9a0d0296d3de165
Autor:
Francesco Brigo, Marta Ponzano, Maria Pia Sormani, Marinella Clerico, Gianmarco Abbadessa, Giovanni Cossu, Francesca Trojsi, Fabiana Colucci, Carla Tortorella, Giuseppina Miele, Emanuele Spina, Carlo Alberto Artusi, Luca Carmisciano, Giovanna Servillo, Marco Bozzali, Maddalena Sparaco, Letizia Leocani, Roberta Lanzillo, Gioacchino Tedeschi, Simona Bonavita, Luigi Lavorgna
Publikováno v:
Therapeutic Advances in Chronic Disease, Vol 12 (2021)
Background: Digital health, including telemedicine, is increasingly recommended for the management of chronic neurological disorders, and it has changed the roles of patients and clinicians. Methods: In this cross-sectional study we aimed to investig
Externí odkaz:
https://doaj.org/article/5d6da00c872044b7b5ce45832d768953
Autor:
Roberto Cilia, Emanuele Cereda, Marco Piatti, Andrea Pilotto, Luca Magistrelli, Nico Golfrè Andreasi, Salvatore Bonvegna, Elena Contaldi, Francesca Mancini, Gabriele Imbalzano, Rosa De Micco, Fabiana Colucci, Arianna Braccia, Gabriele Bellini, Francesco Brovelli, Roberta Zangaglia, Giulia Lazzeri, Maria Claudia Russillo, Enrica Olivola, Chiara Sorbera, Viviana Cereda, Patrizia Pinto, Patrizia Sucapane, Giorgio Gelosa, Mario Meloni, Francesca Pistoia, Maria Sessa, Margherita Canesi, Nicola Modugno, Claudio Pacchetti, Laura Brighina, Maria Teresa Pellecchia, Roberto Ceravolo, Mariachiara Sensi, Maurizio Zibetti, Cristoforo Comi, Alessandro Padovani, Anna L. Zecchinelli, Alessio Di Fonzo, Alessandro Tessitore, Francesca Morgante, Roberto Eleopra
Publikováno v:
Movement Disorders Clinical Practice. 10:625-635
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7d0ae4c3559a2304867cc8808a8f7244
https://doi.org/10.1002/mdc3.13681
https://doi.org/10.1002/mdc3.13681
Autor:
Elena Contaldi, Mariachiara Sensi, Fabiana Colucci, Jay Guido Capone, Arianna Braccia, Mattia Roberto Nocilla, Enrica Diozzi, Eleonora Contini, Anna Chiara Pelizzari, Valeria Tugnoli
Publikováno v:
Neurological Sciences. 44:1597-1606
Background Event-related potentials (ERPs) reflect cognitive processing: negative early components (N100, N200) are involved in the sensory and perceptual processing of a stimulus, whereas late positive component P300 requires conscious attention. Bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a50ff12341b3a084a374e077bdb55da4
https://doi.org/10.1007/s10072-022-06597-5
https://doi.org/10.1007/s10072-022-06597-5
Autor:
Fabiana Colucci, Daniela Di Bella, Chiara Pisciotta, Elisa Sarto, Francesca Gualandi, Marcella Neri, Alessandra Ferlini, Elena Contaldi, Maura Pugliatti, Davide Pareyson, Mariachiara Sensi
Publikováno v:
Neurological Sciences. 43:5095-5098
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b5c559f2adbeffcd67e67320665bb74
https://doi.org/10.1007/s10072-022-06137-1
https://doi.org/10.1007/s10072-022-06137-1
Autor:
Fabiana Colucci, Marcella Neri, Fernanda Fortunato, Alessandra Ferlini, Rosalba Carrozzo, Alessandra Torraco, Eleonora Lamantea, Andrea Legati, Ginevra Tecilla, Maura Pugliatti, Mariachiara Sensi
Publikováno v:
The Cerebellum.
AFG3-like matrix AAA peptidase subunit 2 gene (AFG3L2, OMIM * 604,581) biallelic mutations lead to autosomal recessive spastic ataxia-5 SPAX5, OMIM # 614,487), a rare hereditary form of ataxia. The clinical spectrum includes early-onset cerebellar at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07d106d999efa220739c4c9c70d6c096
https://doi.org/10.1007/s12311-022-01497-y
https://doi.org/10.1007/s12311-022-01497-y
Publikováno v:
Mov Disord Clin Pract
Background: Movement disorders affecting the trunk remain a diagnostic challenge even for experienced clinicians. However, despite being common and debilitating, truncal movement disorders are rarely discussed and poorly reviewed in the medical liter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9613cb102a118a9766021dddc4058430
https://pubmed.ncbi.nlm.nih.gov/34631937
https://pubmed.ncbi.nlm.nih.gov/34631937