Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Giulia D'Alvano"'
Autor:
Francesca Trojsi, Federica Di Nardo, Giulia D'Alvano, Carla Passaniti, Minoo Sharbafshaaer, Fabrizio Canale, Antonio Russo, Marcello Silvestro, Luigi Lavorgna, Mario Cirillo, Fabrizio Esposito, Gioacchino Tedeschi, Mattia Siciliano
Publikováno v:
Brain and Behavior, Vol 13, Iss 7, Pp n/a-n/a (2023)
Abstract Introduction Fatigue is defined as a symptom of exhaustion unexplained by drug effects or psychiatric disorders and comprises two main components (i.e., central or “mental” and peripheral or “physical” components), both influencing g
Externí odkaz:
https://doaj.org/article/c2a7839081af4a578e13927503b85c48
Autor:
Minoo Sharbafshaaer, Daniela Buonanno, Carla Passaniti, Manuela De Stefano, Sabrina Esposito, Fabrizio Canale, Giulia D’Alvano, Marcello Silvestro, Antonio Russo, Gioacchino Tedeschi, Mattia Siciliano, Francesca Trojsi
Publikováno v:
Frontiers in Psychiatry, Vol 13 (2022)
The coronavirus disease 2019 (COVID-19) pandemic confined most of the population to homes worldwide, and then, a lot of amyotrophic lateral sclerosis (ALS) centers moved to telemedicine services to continue to assist both patients with ALS and their
Externí odkaz:
https://doaj.org/article/d882e84adfbf47b089edfcbd50880a55
Autor:
Sabrina Esposito, Francesca Trojsi, Giovanni Cirillo, Manuela de Stefano, Federica Di Nardo, Mattia Siciliano, Giuseppina Caiazzo, Domenico Ippolito, Dario Ricciardi, Daniela Buonanno, Danilo Atripaldi, Roberta Pepe, Giulia D’Alvano, Antonella Mangione, Simona Bonavita, Gabriella Santangelo, Alessandro Iavarone, Mario Cirillo, Fabrizio Esposito, Sandro Sorbi, Gioacchino Tedeschi
Publikováno v:
Biomedicines, Vol 10, Iss 5, p 994 (2022)
Repetitive transcranial magnetic stimulation (rTMS) is a noninvasive neuromodulation technique that is increasingly used as a nonpharmacological intervention against cognitive impairment in Alzheimer’s disease (AD) and other dementias. Although rTM
Externí odkaz:
https://doaj.org/article/dd6df1278d5a42a2ab381578ba0e9bd1
Autor:
Giulia D’Alvano, Daniela Buonanno, Carla Passaniti, Manuela De Stefano, Luigi Lavorgna, Gioacchino Tedeschi, Mattia Siciliano, Francesca Trojsi
Publikováno v:
Brain Sciences, Vol 12, Iss 1, p 49 (2021)
Family caregivers of people with amyotrophic lateral sclerosis (ALS), a severely disabling neurodegenerative disease due to the degeneration of both upper and lower motor neurons, have a very demanding role in managing their relatives, thereby often
Externí odkaz:
https://doaj.org/article/214925f2012b44788ad37fc2202ec23a
Autor:
Francesca Trojsi, Federica Di Nardo, Giulia D’Alvano, Giuseppina Caiazzo, Carla Passaniti, Antonella Mangione, Minoo Sharbafshaaer, Antonio Russo, Marcello Silvestro, Mattia Siciliano, Mario Cirillo, Gioacchino Tedeschi, Fabrizio Esposito
Publikováno v:
Brain Imaging and Behavior. 17:77-89
Background: Pseudobulbar affect (PBA), referring to exaggerated or inappropriate episodes of laughing and/or crying without an apparent motivating stimulus, has been mainly attributed to bilateral degeneration of corticobulbar tracts. We aimed at exp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::319265cf2fe345377f1af32c274f5abd
https://doi.org/10.1007/s11682-022-00744-4
https://doi.org/10.1007/s11682-022-00744-4
Autor:
Fabrizio Esposito, Francesca Trojsi, Giuseppina Caiazzo, Federica Di Nardo, Mattia Siciliano, Carla Passaniti, Giulia D'Alvano, Antonio Russo, Mario Cirillo, Gioacchino Tedeschi, Simona Bonavita
Publikováno v:
Journal of Neural Transmission
The organization of brain functional connectivity (FC) has been shown to differ between sexes. Amyotrophic lateral sclerosis (ALS) is characterized by sexual dimorphism, showing sex-specific trends in site of onset, phenotypes, and prognosis. Here, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6852091f5f8577e23fe6dac914a2502f
https://doi.org/10.1007/s00702-021-02413-0
https://doi.org/10.1007/s00702-021-02413-0
Autor:
Carla Passaniti, Francesca Trojsi, Gabriella Santangelo, Sabrina Esposito, Giuseppina Caiazzo, Fabrizio Esposito, Mario Cirillo, Antonio Russo, Federica Di Nardo, Gioacchino Tedeschi, Luigi Lavorgna, Mattia Siciliano, Teresa Ferrantino, Dario Ricciardi, Giulia D'Alvano, Simona Bonavita
Publikováno v:
Brain Imaging and Behavior
Emerging evidence suggests that memory deficit in amyotrophic lateral sclerosis (ALS), a neurodegenerative disease with varying impairment of motor abilities and cognitive profile, may be independent from executive dysfunction. Our multimodal magneti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9057c74300bf31e2c36cfa3fb9c601b4
https://doi.org/10.1007/s11682-020-00408-1
https://doi.org/10.1007/s11682-020-00408-1
Autor:
Antonio Russo, Francesca Trojsi, Simona Bonavita, Giulia D'Alvano, Mattia Siciliano, Mario Cirillo, Alvino Bisecco, Gioacchino Tedeschi, Giuseppina Caiazzo, Dario Ricciardi, Carla Passaniti, Luigi Lavorgna, Federica Di Nardo, Fabrizio Esposito
Publikováno v:
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 22:117-126
Objective: Advanced neuroimaging techniques may offer the potential to monitor disease spreading in amyotrophic lateral sclerosis (ALS). We aim to investigate brain functional and structural magnetic resonance imaging (MRI) changes in a cohort of ALS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a36ddd6b9742ab1f579bd0c2e30c68c4
https://doi.org/10.1080/21678421.2020.1813306
https://doi.org/10.1080/21678421.2020.1813306
Autor:
Giulia D’Alvano, Daniela Buonanno, Carla Passaniti, Manuela De Stefano, Luigi Lavorgna, Gioacchino Tedeschi, Mattia Siciliano, Francesca Trojsi
Publikováno v:
Brain Sciences, Vol 12, Iss 49, p 49 (2022)
Brain Sciences
Brain Sciences
Family caregivers of people with amyotrophic lateral sclerosis (ALS), a severely disabling neurodegenerative disease due to the degeneration of both upper and lower motor neurons, have a very demanding role in managing their relatives, thereby often
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ab75a6c94d82e581f03583e689ffbde
http://hdl.handle.net/11591/470414
http://hdl.handle.net/11591/470414
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 21, Iss 3647, p 3647 (2020)
International Journal of Molecular Sciences, Vol 21, Iss 3647, p 3647 (2020)
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease with no known cure. Approximately 90% of ALS cases are sporadic, although multiple genetic risk factors have been recently revealed also in sporadic ALS (SALS). The pathological
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c2a004945abac46ce01cfe8cb7cdb66
http://europepmc.org/articles/PMC7279172
http://europepmc.org/articles/PMC7279172