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Wyszukujesz frazę ""Scaioli, V."" wg kryterium: Wszystkie pola


Tytuł :
SCN8A splicing mutation causing skipping of the exon 15 associated with intellectual disability and cortical myoclonus.
Autorzy :
Canafoglia L; Unit of Integrated Diagnostics for Epilepsy, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy(1).
Franceschetti S; Unit of Neurophysiopathology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy(1). Electronic address: .
Granata T; Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy(1).
Messina G; Unit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Solazzi R; Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy(1).
Ragona F; Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy(1).
Freri E; Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy(1).
Scaioli V; Unit of Neurophysiopathology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy(1).
Nardocci N; Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy(1).
Gellera C; Unit of Neurophysiopathology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy(1).
Panzica F; Biomedical Engineering, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
DiFrancesco JC; Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy(1); Department of Neurology, San Gerardo Hospital, School of Medicine and Surgery, Milan Center for Neuroscience (NeuroMi), University of Milano-Bicocca, Monza, Italy.
Castellotti B; Unit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
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Źródło :
Seizure [Seizure] 2020 Nov; Vol. 82, pp. 56-58. Date of Electronic Publication: 2020 Sep 23.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Early Parkinsonism in a Senegalese girl with Lafora disease.
Autorzy :
Ragona F; Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Member of the ERN EpiCARE, Milano.
Canafoglia L; Neurophysiopathology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano.
Castellotti B; Unit of Genetics of Neurodegenerative and Metabolic Diseases, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano.
Solazzi R; Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Member of the ERN EpiCARE, Milano.
Gabbiadini S; Unit of Child Neuropsychiatry, Ospedale Papa Giovanni XXIII, Bergamo.
Freri E; Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Member of the ERN EpiCARE, Milano.
Scaioli V; Neurophysiopathology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano.
DiFrancesco JC; Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Member of the ERN EpiCARE, Milano, Department of Neurology and Epilepsy Center, Milan Center for Neuroscience, San Gerardo Hospital, University of Milano-Bicocca, Monza, Italy.
Gellera C; Unit of Genetics of Neurodegenerative and Metabolic Diseases, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano.
Granata T; Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Member of the ERN EpiCARE, Milano.
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Źródło :
Epileptic disorders : international epilepsy journal with videotape [Epileptic Disord] 2020 Apr 01; Vol. 22 (2), pp. 233-236.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Cognitive Dysfunction*/etiology
Cognitive Dysfunction*/physiopathology
Lafora Disease*/complications
Lafora Disease*/genetics
Lafora Disease*/physiopathology
Parkinsonian Disorders*/etiology
Parkinsonian Disorders*/physiopathology
Adolescent ; Electroencephalography ; Evoked Potentials/physiology ; Female ; Humans ; Retina/physiopathology ; Senegal ; Ubiquitin-Protein Ligases/genetics
Czasopismo naukowe
Tytuł :
Event-related potential (ERP) markers of melodic processing: The N2 component is modulated by structural complexity, not by melodic ‘meaningfulness’
Autorzy :
Minati, L.
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Źródło :
In Brain Research Bulletin 2010 83(1):23-28
Czasopismo naukowe
Tytuł :
Guillain-Barré Syndrome After Exposure to Mercury.
Autorzy :
Pigatto PD; Department of Biomedical, Surgical and Dental Sciences, IRCCS Istituto Ortopedico Galeazzi, University of Milan, Milan, Italy.
Scaioli V; UOC Neurology, Clinical Neurophysiology, Besta Institute Foundation IRCCS, Milan, Italy.
Guzzi G; Italian Association for Metals and Biocompatibility Research - A.I.R.M.E.B., Milan, Italy.
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Źródło :
Journal of child neurology [J Child Neurol] 2020 Jan; Vol. 35 (1), pp. 84-85. Date of Electronic Publication: 2019 Sep 27.
Typ publikacji :
Letter
Opinia redakcyjna

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