Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Daniele, Grioni"'
Autor:
Giulia Melinda Furlanis, Jacopo Favaro, Nicola Bresolin, Daniele Grioni, Valentina Baro, Alberto D’Amico, Stefano Sartori, Luca Denaro, Andrea Landi
Publikováno v:
Brain Sciences, Vol 13, Iss 11, p 1589 (2023)
Background: Status epilepticus is a life-threatening condition that is defined as refractory (RSE) when the seizure activity continues despite treatment with benzodiazepine and a second appropriate treatment. Super refractory status epilepticus (SRSE
Externí odkaz:
https://doaj.org/article/78de740de4304a129649022a53a5c008
Autor:
Valentina Baro, Maria Vittoria Bonavina, Francesco Saettini, Giovanna D’Amico, Andrea Trezza, Luca Denaro, Daniele Grioni, Andrea Landi
Publikováno v:
Children, Vol 9, Iss 8, p 1133 (2022)
Background: Since one of the suggested mechanisms of action of VNS on epilepsy is the reduction of central inflammation, we carried out a comprehensive analysis of blood inflammatory markers in children considered for VNS surgery. Materials and metho
Externí odkaz:
https://doaj.org/article/610ab1cb7d9446e7b9d157c0a0f2b34a
Autor:
Rossella Parini, Miriam Rigoldi, Lucia Tedesco, Lucia Boffi, Alessandra Brambilla, Sara Bertoletti, Agata Boncimino, Alessandra Del Longo, Paola De Lorenzo, Renato Gaini, Denise Gallone, Serena Gasperini, Carlo Giussani, Marco Grimaldi, Daniele Grioni, Pamela Meregalli, Grazia Messinesi, Francesca Nichelli, Marco Romagnoli, Pierluigi Russo, Erik Sganzerla, Grazia Valsecchi, Andrea Biondi
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 3, Iss C, Pp 65-74 (2015)
Hunter disease is an X-linked lysosomal storage disorder characterized by progressive storage of glycosaminoglycans (GAGs) and multi-organ impairment. The central nervous system (CNS) is involved in at least 50% of cases. Since 2006, the enzymatic re
Externí odkaz:
https://doaj.org/article/498ce9393d9048e4a561a231caf612c9
Autor:
Agata Fiumara, Roberta Epifanio, Veronica Di Pisa, Chiara Pantaleoni, Patrizia Accorsi, Nicoletta Zanotta, Erica Finardi, Paolo Bonanni, Daniele Grioni, Federico Raviglione, Livia Garavelli, Salvatore Savasta, Emilia Ricci, Francesca Faravelli, Stefano Giuseppe Caraffi, Luigi Tarani, Ivan Ivanovski, Daniela Chiarello, Francesca Rivieri, Isabella Mammi, Anna Fetta, Silvia Bonetti, Antonella Boni, Ada Dormi, Elisa Osanni, Alessia Arena, Duccio Maria Cordelli, Antonino Romeo, Lucio Giordano, Aglaia Vignoli, R. Rizzi, Maria Paola Canevini, Susanna Negrin
Publikováno v:
Epilepsybehavior : EB. 124
Background Epilepsy is a main feature of Mowat Wilson Syndrome (MWS), a congenital malformation syndrome caused by ZEB2 variants. The aim of this study was to investigate the long-term evolution of the electroclinical phenotype of MWS in a large popu
Autor:
Patrizia Accorsi, Federica Provini, Emilia Ricci, Claudio Graziano, Ivan Ivanovski, Veronica Di Pisa, Livia Garavelli, Federico Raviglione, Silvia Bonetti, Daniele Grioni, Antonella Boni, Salvatore Savasta, Stefano Giuseppe Caraffi, Duccio Maria Cordelli, Lucio Giordano, Sara Ubertiello
Objective Sleep disturbances are frequently reported in Mowat-Wilson Syndrome (MWS). The current study aimed to evaluate clinical and video-polysomnographic (VPSG) characteristics of the sleep architecture and abnormal electroencephalogram (EEG) patt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05db28f38dac20ad3f8073f0ea003950
http://hdl.handle.net/11585/698327
http://hdl.handle.net/11585/698327
Autor:
Andrea Landi, Daniele Grioni
Publikováno v:
World neurosurgery. 121
Purpose Status Epilepticus can be a serious life threatening event in epileptic patients. The definition of refractory or super-refractory Status Epilepticus was based on the therapeutic response to anti-epileptic and anesthetic drugs. Vagal Nerve St
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8733273a5cd2630bbbb747ef39a563ad
http://hdl.handle.net/10281/244962
http://hdl.handle.net/10281/244962
Autor:
M Grimaldi, Grazia Messinesi, Grazia Valsecchi, Andrea Biondi, Denise Gallone, Renato Maria Gaini, Alessandra Brambilla, Erik P. Sganzerla, Carlo Giussani, Paola De Lorenzo, Miriam Rigoldi, Lucia Tedesco, Rossella Parini, Pamela Meregalli, Lucia Boffi, Marco Romagnoli, Francesca Nichelli, Pierluigi Russo, Agata Boncimino, Daniele Grioni, Serena Gasperini, Alessandra Del Longo, Sara Bertoletti
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 3, Iss C, Pp 65-74 (2015)
Molecular Genetics and Metabolism Reports, Vol 3, Iss C, Pp 65-74 (2015)
Hunter disease is an X-linked lysosomal storage disorder characterized by progressive storage of glycosaminoglycans (GAGs) and multi-organ impairment. The central nervous system (CNS) is involved in at least 50% of cases. Since 2006, the enzymatic re
Autor:
Attilio Rovelli, Fabio Pavan, Carlo De Grandi, Francesco Canonico, Daniele Grioni, Giulia Prunotto
Publikováno v:
Neuropediatrics. 48(2)
Despite a wide number of studies trying to define clinical, physiopathological, and neuroradiological features of posterior reversible encephalopathy syndrome (PRES), the true nature of symptoms is still not fully understood. We studied a standard co
Autor:
Giulio Sancini, Mauro Toselli, R. Rusconi, Chiara Villa, Daniele Grioni, Veronica Sansoni, Francesca Talpo, Massimo Mantegazza, N. Binini, R Dal Magro, Romina Combi
Publikováno v:
Brain research 1677, 26-32 (2017). doi:10.1016/j.brainres.2017.09.023
Mutations in the SCN1A gene causing either loss or gain of function have been frequently found in patients affected by genetic epilepsy with febrile seizures plus (GEFS+) or Dravet syndrome (also named severe myoclonic epilepsy in infancy SMEI). By m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18ae09fc3161001c10f2d213d8c0d121