Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Dalila de Vita"'
Autor:
Dalila De Vita
Publikováno v:
Premio Tesi di Dottorato ISBN: 9788855183437
Malformations of cortical development (MCDs) result from a disruption in the process of the human brain cortex formation: currently, there are no pharmacological treatments for diffuse MCDs. Next-generation sequencing has accelerated the identificati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99cc651391e3c2b2769892c1668a5a28
https://doi.org/10.36253/978-88-5518-344-4
https://doi.org/10.36253/978-88-5518-344-4
Autor:
Alessandro Iavarone, Alfredo Postiglione, Alessia Coppola, Marzia De Luca, Sara Sorrentino, Flavia Lualdi, Sabina Raimondo, Rosa Scarpa, Dalila de Vita, Caterina Musella, Stefano Branciforte, Michele Carpinelli Mazzi
Publikováno v:
European Geriatric Medicine
Key summary points Aim To evaluate the effects of the COVID-19 emergency lockdown on the psychological outcome in caregivers of patients with dementia and on the loss of welfare services in these patients. Findings Time of isolation, education and ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c45c78e731ae2716d60e2e339c74720d
https://pubmed.ncbi.nlm.nih.gov/33052535
https://pubmed.ncbi.nlm.nih.gov/33052535
In the last years, several studies using non-invasive brain stimulation (NIBS) techniques demonstrated that the dorsolateral prefrontal cortex (DLPFC) plays a key role in the neurobiological bases of anxiety disorders. Both transcranial magnetic stim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c76232fc859ce58c5d8d9c401798981a
http://hdl.handle.net/11591/405053
http://hdl.handle.net/11591/405053
Autor:
Domenico Rutigliano, Dalila De Vita, Niccolò Bartalucci, Elena Parrini, Davide Mei, Robertino Dilena, Claudia Cinnante, Renzo Guerrini
Publikováno v:
American journal of medical genetics. Part A. 176(12)
We describe a mother and son with focal epilepsy, mild cognitive impairment, and pachygyria, which was parieto-occipital in the mother and with remarkable posterior greater than anterior severity in the son. Overall clinical manifestations, although
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::475e44cf6f10817d993c93d8982c8eb3
https://pubmed.ncbi.nlm.nih.gov/30144370
https://pubmed.ncbi.nlm.nih.gov/30144370
Autor:
Carla, Marini, Michele, Romoli, Elena, Parrini, Cinzia, Costa, Davide, Mei, Francesco, Mari, Lucio, Parmeggiani, Elena, Procopio, Tiziana, Metitieri, Elena, Cellini, Simona, Virdò, Dalila, De Vita, Mattia, Gentile, Paolo, Prontera, Paolo, Calabresi, Renzo, Guerrini
Publikováno v:
Neurology: Genetics
Objective: To describe electroclinical features and outcome of 6 patients harboring KCNB1 mutations. Methods: Clinical, EEG, neuropsychological, and brain MRI data analysis. Targeted next-generation sequencing of a 95 epilepsy gene panel. Results: Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fd8a342e950d4b863e75b615aa12a1e5
https://pubmed.ncbi.nlm.nih.gov/29264397
https://pubmed.ncbi.nlm.nih.gov/29264397
Autor:
Elena Cellini, Elena Parrini, Paolo Calabresi, Michele Romoli, Lucio Parmeggiani, Renzo Guerrini, Francesco Mari, Tiziana Metitieri, Mattia Gentile, Simona Virdò, Elena Procopio, Dalila De Vita, Paolo Prontera, Cinzia Costa, Davide Mei, Carla Marini
Publikováno v:
Neurology Genetics. 3:e206
Objective:To describe electroclinical features and outcome of 6 patients harboring KCNB1 mutations.Methods:Clinical, EEG, neuropsychological, and brain MRI data analysis. Targeted next-generation sequencing of a 95 epilepsy gene panel.Results:The mea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa5d8a84b8d29a1d7cfc42b9ccf3d267
https://doi.org/10.1212/nxg.0000000000000206
https://doi.org/10.1212/nxg.0000000000000206