Results 11 to 20 of about 1,704,825 (163)

A monad for full ground reference cells [PDF]

2017 32nd Annual ACM/IEEE Symposium on Logic in Computer Science (LICS), 2017
We present a denotational account of dynamic allocation of potentially cyclic memory cells using a monad on a functor category. We identify the collection of heaps as an object in a different functor category equipped with a monad for adding hiding/encapsulation capabilities to the heaps.
Kammar, O, Levy, P, Moss, S, Staton, S
openaire   +3 more sources

TELEmedicine for EPIlepsy Care (TELE-EPIC): protocol of a randomised, open controlled non-inferiority clinical trial

BMJ Open, 2021
Introduction Epilepsy is a chronic condition requiring consistent follow-up aimed at seizure control, and monitoring of anti-seizure medication (ASM) levels and side effects.
Emanuel Raschi, Corrado Zenesini, Federico Vigevano, Elisa Baldin, Paolo Tinuper, Manuela Contin, Barbara Mostacci, Susan Mohamed, Luca Vignatelli   +8 more
doaj   +1 more source

POLG1-Related Epilepsy: Review of Diagnostic and Therapeutic Findings

Brain Sciences, 2020
Background: The clinical spectrum associated with POLG1 gene mutations ranges from non-syndromic epilepsy or mild isolated neurological signs to neurodegenerative disorders.
Nicola Specchio, Nicola Pietrafusa, Costanza Calabrese, Marina Trivisano, Chiara Pepi, Luca de Palma, Alessandro Ferretti, Paolo Curatolo, Federico Vigevano   +8 more
doaj   +1 more source

Fatal Status Epilepticus in Dravet Syndrome

Brain Sciences, 2020
Dravet Syndrome (DS) is burdened by high epilepsy-related premature mortality due to status epilepticus (SE). We surveyed centres within Europe through the Dravet Italia Onlus and EpiCARE network (European Reference Network for Rare and Complex ...
Paola De Liso, Virginia Pironi, Massimo Mastrangelo, Domenica Battaglia, Dana Craiu, Marina Trivisano, Nicola Specchio, Rima Nabbout, Federico Vigevano   +8 more
doaj   +1 more source

Prognostic value of pathogenic variants in Lafora Disease: systematic review and meta-analysis of patient-level data

Orphanet Journal of Rare Diseases, 2023
Background Lafora disease (LD) is a fatal form of progressive myoclonic epilepsy caused by biallelic pathogenic variants in EPM2A or NHLRC1. With a few exceptions, the influence of genetic factors on disease progression has yet to be confirmed.
Federica Pondrelli, Raffaella Minardi, Lorenzo Muccioli, Corrado Zenesini, Luca Vignatelli, Laura Licchetta, Barbara Mostacci, Paolo Tinuper, Craig W. Vander Kooi, Matthew S. Gentry, Francesca Bisulli   +10 more
doaj   +1 more source

Subjective and Objective Quality Assessment of High Frame Rate Videos

IEEE Access, 2021
High frame rate (HFR) videos are becoming increasingly common with the tremendous popularity of live, high-action streaming content such as sports.
Pavan C. Madhusudana, Xiangxu Yu, Neil Birkbeck, Yilin Wang, Balu Adsumilli, Alan C. Bovik   +5 more
doaj   +1 more source

Modular Framework and Instances of Pixel-Based Video Quality Models for UHD-1/4K

IEEE Access, 2021
The popularity of video on-demand streaming services increased tremendously over the last years. Most services use http-based adaptive video streaming methods.
Steve Goring, Rakesh Rao Ramachandra Rao, Bernhard Feiten, Alexander Raake   +3 more
doaj   +1 more source

Imbalance of Systemic Redox Biomarkers in Children with Epilepsy: Role of Ferroptosis

Antioxidants, 2021
To assess if ferroptosis, a new type of programmed cell death accompanied by iron accumulation, lipid peroxidation, and glutathione depletion, occurs in children with epilepsy, and in order to identify a panel of biomarkers useful for patient ...
Sara Petrillo, Nicola Pietrafusa, Marina Trivisano, Costanza Calabrese, Francesca Saura, Maria Giovanna Gallo, Enrico Silvio Bertini, Federico Vigevano, Nicola Specchio, Fiorella Piemonte   +9 more
doaj   +1 more source

Epilepsy and inborn errors of metabolism in adults: The diagnostic odyssey of a young woman with medium‐chain acyl‐coenzyme A dehydrogenase deficiency

Epilepsia Open, 2022
We describe a case of epileptic encephalopathy in a young woman with undiagnosed medium‐chain acyl‐coenzyme A dehydrogenase deficiency (MCADD), who presented with an early‐onset focal motor status epilepticus (SE) then followed by permanent left ...
Ilaria Cani, Federica Pondrelli, Laura Licchetta, Raffaella Minardi, Tania Giangregorio, Barbara Mostacci, Lorenzo Muccioli, Lidia Di Vito, Anna Fetta, Carmen Barba, Carlo Alberto Castioni, Andrea Bordugo, Paolo Tinuper, Francesca Bisulli   +13 more
doaj   +1 more source

Hemispherotomy in Infants with Hemimegalencephaly: Long-Term Seizure and Developmental Outcome in Early Treated Patients

Brain Sciences, 2022
Hemimegalencephaly (HME) is a rare brain congenital malformation, consisting in altered neuronal migration and proliferation within one hemisphere, which is responsible for early onset drug-resistant epilepsy.
Chiara Pepi, Alessandro De Benedictis, Maria Camilla Rossi-Espagnet, Simona Cappelletti, Martina Da Rold, Giovanni Falcicchio, Federico Vigevano, Carlo Efisio Marras, Nicola Specchio, Luca De Palma   +9 more
doaj   +1 more source