Zobrazeno 1 - 10
of 93
pro vyhledávání: '"Marina, Grisoli"'
Autor:
Davide Fedeli, Giuseppe Ciullo, Greta Demichelis, Jean Paul Medina Carrion, Maria Grazia Bruzzone, Emilio Ciusani, Alessandra Erbetta, Stefania Ferraro, Marina Grisoli, Erika Guastafierro, Domenico D’Amico, Alberto Raggi, Anna Nigri, Licia Grazzi
Publikováno v:
The Journal of Headache and Pain, Vol 25, Iss 1, Pp 1-12 (2024)
Abstract Background Mindfulness practice has gained interest in the management of Chronic Migraine associated with Medication Overuse Headache (CM-MOH). Mindfulness is characterized by present-moment self-awareness and relies on attention control and
Externí odkaz:
https://doaj.org/article/45eb8b47dea4455a94bcc7661a2e9352
Autor:
Mario Stanziano, Davide Fedeli, Umberto Manera, Stefania Ferraro, Jean P. Medina Carrion, Sara Palermo, Paola Sciortino, Maurizio Cogoni, Federica Agosta, Silvia Basaia, Massimo Filippi, Marina Grisoli, Maria C. Valentini, Filippo De Mattei, Antonio Canosa, Andrea Calvo, Maria G. Bruzzone, Adriano Chiò, Anna Nigri, Cristina Moglia
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 3, Pp 686-697 (2024)
Abstract Objective The resting‐state functional connectome has not been extensively investigated in amyotrophic lateral sclerosis (ALS) spectrum disease, in particular in relationship with patients' genetic status. Methods Here we studied the netwo
Externí odkaz:
https://doaj.org/article/68b52a1f10cc4004a9173b7b27d00b3c
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:
Giuseppe Di Fede, Marcella Catania, Cristiana Atzori, Fabio Moda, Claudio Pasquali, Antonio Indaco, Marina Grisoli, Marta Zuffi, Maria Cristina Guaita, Roberto Testi, Stefano Taraglio, Maria Sessa, Graziano Gusmaroli, Mariacarmela Spinelli, Giulia Salzano, Giuseppe Legname, Roberto Tarletti, Laura Godi, Maurizio Pocchiari, Fabrizio Tagliavini, Daniele Imperiale, Giorgio Giaccone
Publikováno v:
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-11 (2019)
Abstract Prion diseases are neurodegenerative disorders which are caused by an accumulation of the abnormal, misfolded prion protein known as scrapie prion protein (PrPSc). These disorders are unique as they occur as sporadic, genetic and acquired fo
Externí odkaz:
https://doaj.org/article/46afdf2fd23547ffa41d811b6d180715
Autor:
Anna Nigri, Lidia Sarro, Alessia Mongelli, Chiara Pinardi, Luca Porcu, Anna Castaldo, Stefania Ferraro, Marina Grisoli, Maria Grazia Bruzzone, Cinzia Gellera, Franco Taroni, Caterina Mariotti, Lorenzo Nanetti
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Spinocerebellar ataxias type 2 (SCA2) is an autosomal dominant inherited disease caused by expanded trinucleotide repeats (≥32 CAG) within the coding region of ATXN2 gene. Age of disease onset primarily depends on the length of the expanded region.
Externí odkaz:
https://doaj.org/article/0bef9478f641413f83fe1c7ca770bf4d
Autor:
Lorenzo Nanetti, Stefania Magri, Mario Fichera, Anna Castaldo, Anna Nigri, Chiara Pinardi, Alessia Mongelli, Lidia Sarro, Davide Pareyson, Marina Grisoli, Cinzia Gellera, Daniela Di Bella, Caterina Mariotti, Franco Taroni
Publikováno v:
Movement Disorders. 38:665-675
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::089f0352bc25d28c491c0ba4e9cf8606
https://doi.org/10.1002/mds.29352
https://doi.org/10.1002/mds.29352
Autor:
Carole H. Sudre, Martina Bocchetta, David Cash, David L. Thomas, Ione Woollacott, Katrina M. Dick, John van Swieten, Barbara Borroni, Daniela Galimberti, Mario Masellis, Maria Carmela Tartaglia, James B. Rowe, Caroline Graff, Fabrizio Tagliavini, Giovanni Frisoni, Robert Laforce, Jr, Elizabeth Finger, Alexandre de Mendonça, Sandro Sorbi, Sébastien Ourselin, M. Jorge Cardoso, Jonathan D. Rohrer, Christin Andersson, Silvana Archetti, Andrea Arighi, Luisa Benussi, Giuliano Binetti, Sandra Black, Maura Cosseddu, Marie Fallström, Carlos Ferreira, Chiara Fenoglio, Nick C. Fox, Morris Freedman, Giorgio Fumagalli, Stefano Gazzina, Roberta Ghidoni, Marina Grisoli, Vesna Jelic, Lize Jiskoot, Ron Keren, Gemma Lombardi, Carolina Maruta, Simon Mead, Lieke Meeter, Rick van Minkelen, Benedetta Nacmias, Linn Öijerstedt, Alessandro Padovani, Jessica Panman, Michela Pievani, Cristina Polito, Enrico Premi, Sara Prioni, Rosa Rademakers, Veronica Redaelli, Ekaterina Rogaeva, Giacomina Rossi, Martin N. Rossor, Elio Scarpini, David Tang-Wai, Hakan Thonberg, Pietro Tiraboschi, Ana Verdelho, Jason D. Warren
Publikováno v:
NeuroImage: Clinical, Vol 15, Iss , Pp 171-180 (2017)
Genetic frontotemporal dementia is most commonly caused by mutations in the progranulin (GRN), microtubule-associated protein tau (MAPT) and chromosome 9 open reading frame 72 (C9orf72) genes. Previous small studies have reported the presence of cere
Externí odkaz:
https://doaj.org/article/a89b4ebcd4f642b09beae4a74ef4772a
Autor:
Vikram Venkatraghavan, Riccardo Pascuzzo, Esther E. Bron, Marco Moscatelli, Marina Grisoli, Amy Pickens, Mark L. Cohen, Lawrence B. Schonberger, Pierluigi Gambetti, Brian S. Appleby, Stefan Klein, Alberto Bizzi
Publikováno v:
Alzheimer's and Dementia. Elsevier Inc.
Venkatraghavan, V, Pascuzzo, R, Bron, E E, Moscatelli, M, Grisoli, M, Pickens, A, Cohen, M L, Schonberger, L B, Gambetti, P, Appleby, B S, Klein, S & Bizzi, A 2023, ' A discriminative event-based model for subtype diagnosis of sporadic Creutzfeldt-Jakob disease using brain MRI ', Alzheimer's and Dementia . https://doi.org/10.1002/alz.12939
Alzheimer's and Dementia. Elsevier
Venkatraghavan, V, Pascuzzo, R, Bron, E E, Moscatelli, M, Grisoli, M, Pickens, A, Cohen, M L, Schonberger, L B, Gambetti, P, Appleby, B S, Klein, S & Bizzi, A 2023, ' A discriminative event-based model for subtype diagnosis of sporadic Creutzfeldt-Jakob disease using brain MRI ', Alzheimer's and Dementia . https://doi.org/10.1002/alz.12939
Alzheimer's and Dementia. Elsevier
Introduction: Sporadic Creutzfeldt-Jakob disease (sCJD) comprises multiple subtypes (MM1, MM2, MV1, MV2C, MV2K, VV1, and VV2) with distinct disease durations and spatiotemporal cascades of brain lesions. Our goal was to establish the ante mortem diag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f1fcd0a44219e175387db8a10837134
http://www.scopus.com/inward/record.url?scp=85147535168&partnerID=8YFLogxK
http://www.scopus.com/inward/record.url?scp=85147535168&partnerID=8YFLogxK
Autor:
Matteo Figini, Daniel C. Alexander, Veronica Redaelli, Fabrizio Fasano, Marina Grisoli, Giuseppe Baselli, Pierluigi Gambetti, Fabrizio Tagliavini, Alberto Bizzi
Publikováno v:
NeuroImage: Clinical, Vol 7, Iss C, Pp 142-154 (2015)
In clinical practice signal hyperintensity in the cortex and/or in the striatum on magnetic resonance (MR) diffusion-weighted images (DWIs) is a marker of sporadic Creutzfeldt–Jakob Disease (sCJD). MR diagnostic accuracy is greater than 90%, but th
Externí odkaz:
https://doaj.org/article/aa9419ce87db4ec88f6b71c2c8a1e6e6