Zobrazeno 1 - 10
of 538
pro vyhledávání: '"Giancarlo Logroscino"'
Autor:
Roberta Barone, Giulia Bramato, Valentina Gnoni, Alessia Giugno, Daniele Urso, Chiara Zecca, Salvatore Nigro, Marco Filardi, Giancarlo Logroscino
Publikováno v:
BMC Geriatrics, Vol 24, Iss 1, Pp 1-8 (2024)
Abstract Background Sarcopenia is an age-related clinical syndrome characterized by the progressive loss of muscle mass and muscle strength. It appears to be closely linked to dementia, particularly Alzheimer’s disease (AD); however, its prevalence
Externí odkaz:
https://doaj.org/article/c67aa9dfd1b74aadaed5914964ac3bd5
Publikováno v:
BMJ Open, Vol 14, Iss 7 (2024)
Introduction Behavioural variant frontotemporal dementia (bvFTD) characterisation has evolved, but diagnosis remains challenging, relying on clinical diagnostic criteria that have undergone revisions over time. In this systematic review, our aims are
Externí odkaz:
https://doaj.org/article/9a42f7b8cca5468a8a1d05559305e177
Publikováno v:
Frontiers in Systems Neuroscience, Vol 18 (2024)
IntroductionPrimary Progressive Aphasia (PPA) is a neurodegenerative disease characterized by linguistic impairment. The two main clinical subtypes are semantic (svPPA) and non-fluent/agrammatic (nfvPPA) variants. Diagnosing and classifying PPA patie
Externí odkaz:
https://doaj.org/article/12a007f83b4d49b4af7b704c250b5e30
Autor:
Stefano Zoccolella, Giammarco Milella, Alessia Giugno, Vito Devitofrancesco, Rosaria Damato, Ludovica Tamburrino, Salvatore Misceo, Marco Filardi, Giancarlo Logroscino
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
BackgroundSplit phenomena (SP) are characterized by patterns of differential muscle wasting and atrophy, which are highly prevalent in amyotrophic lateral sclerosis (ALS) patients. Several neurophysiological indicators, including the split-hand index
Externí odkaz:
https://doaj.org/article/4df83fef96804611a336b61305508706
Autor:
Alma Ghirelli, Benedetta Tafuri, Daniele Urso, Giammarco Milella, Roberto De Blasi, Salvatore Nigro, Giancarlo Logroscino, for the Frontotemporal Lobar Degeneration Neuroimaging Initiative
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 10, Iss 10, Pp 1704-1713 (2023)
Abstract Background and Objectives Depressive symptoms are frequently reported in patients affected by frontotemporal dementia (FTD). At structural MRI, cortical features of depressed FTD patients have been poorly described. Our objective was to inve
Externí odkaz:
https://doaj.org/article/38d696e1bc434b88be72b67e5928136c
Autor:
Benedetta Tafuri, Daniele Urso, Salvatore Nigro, Luigi Macchitella, Roberto De Blasi, K. Ray Chaudhuri, Giancarlo Logroscino
Publikováno v:
npj Parkinson's Disease, Vol 9, Iss 1, Pp 1-7 (2023)
Abstract Loss of empathy is an early and central symptom of frontotemporal lobar degeneration spectrum diseases. We aimed to investigate the topographical distribution of morphometric brain changes associated with empathy in Progressive Supranuclear
Externí odkaz:
https://doaj.org/article/1b79ad8eea024c0c8cbb716818ff531a
Autor:
Barbara Borroni, Ilenia Libri, Matteo Rota, Giuliano Binetti, Luisa Benussi, Roberta Ghidoni, Maria Sofia Cotelli, Silvia Fostinelli, Fabio Guerini, Stefano Boffelli, Eugenio Magni, Marta Pengo, Michele Gennuso, Marta Bianchi, Beatrice Cossu, Vincenzo Palomba, Andrea Crucitti, Angelo Bianchetti, Giancarlo Logroscino, Alessandro Padovani
Publikováno v:
Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring, Vol 16, Iss 1, Pp n/a-n/a (2024)
Abstract INTRODUCTION The goal of the present work was to assess the incidence of dementia with onset before the age of 65 years (i.e., young‐onset dementia [YOD]) and define the frequencies of young‐onset Alzheimer's disease (AD), frontotemporal
Externí odkaz:
https://doaj.org/article/4a35113796634c67943b06b0c73eedd5
Autor:
Francesca Malerba, Rita Florio, Ivan Arisi, Chiara Zecca, Maria Teresa Dell’Abate, Giancarlo Logroscino, Antonino Cattaneo
Publikováno v:
Frontiers in Aging Neuroscience, Vol 15 (2024)
IntroductionFrontotemporal dementia (FTD) is an extremely heterogeneous and complex neurodegenerative disease, exhibiting different phenotypes, genetic backgrounds, and pathological states. Due to these characteristics, and to the fact that clinical
Externí odkaz:
https://doaj.org/article/a24619c53d5c4edca209e684e795b7a1
Autor:
Federico Emanuele Pozzi, Luisa Calì, Fabrizia D'Antonio, Arianna Ida Altomare, Micaela Sepe Monti, Massimiliano Panigutti, Adolfo Di Crosta, Rocco Palumbo, Laura Bonanni, Valentina Carlucci, Cinzia Bussè, Annachiara Cagning, Daniele Urso, Davide Vilella, Giancarlo Logroscino, Margherita Alberoni, Angelo Bellinvia, Elisabetta Farina, Francesca de Rino, Armando Gavazzi, Marta Zuffi, Giuseppe Bruno, Valentina Bessi, Matteo Cotta Ramusino, Giulia Perini, Alfredo Costa, Carlo Ferrarese, Ildebrando Appollonio, Lucio Tremolizzo
Publikováno v:
Frontiers in Dementia, Vol 2 (2023)
Behavioral and Psychological Symptoms of Dementia (BPSD) are a heterogeneous set of psychological and behavioral abnormalities seen in persons with dementia (PwD), significantly impacting their quality of life and that of their caregivers. Current as
Externí odkaz:
https://doaj.org/article/f4e0b01f831b49ee81437c1a17a3d9d8
Autor:
Rosangela Ferese, Simona Scala, Antonio Suppa, Rosa Campopiano, Francesco Asci, Alessandro Zampogna, Maria Antonietta Chiaravalloti, Annamaria Griguoli, Marianna Storto, Alba Di Pardo, Emiliano Giardina, Stefania Zampatti, Francesco Fornai, Giuseppe Novelli, Mirco Fanelli, Chiara Zecca, Giancarlo Logroscino, Diego Centonze, Stefano Gambardella
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
IntroductionPure hereditary spastic paraplegia (SPG) type 4 (SPG4) is caused by mutations of SPAST gene. This study aimed to analyze SPAST variants in SPG4 patients to highlight the occurrence of splicing mutations and combine functional studies to a
Externí odkaz:
https://doaj.org/article/cd13a9fba9c44771b550bdb4a169ec6c