Zobrazeno 1 - 10
of 199
pro vyhledávání: '"Edoardo Ferlazzo"'
Autor:
Oreste Marsico, Angelo Pascarella, Sara Gasparini, Lucia Manzo, Valentina Bova, Vittoria Cianci, Anna Mammì, Domenico Abelardo, Emilio Africa, Giuseppe La Torre, Antonio Armentano, Payam Tabaee Damavandi, Jacopo C. DiFrancesco, Umberto Aguglia, Edoardo Ferlazzo
Publikováno v:
Epilepsia Open, Vol 9, Iss 5, Pp 1723-1730 (2024)
Abstract Objective Epileptic seizures occurring in late adulthood often remain of unknown origin. Sporadic cerebral amyloid angiopathy (CAA) is a cerebral small vessel disease characterized by intracerebral hemorrhage, microhemorrhage and superficial
Externí odkaz:
https://doaj.org/article/918d688a01ef49a1a5f24a905101244d
Autor:
Antonella Riva, Gianluca D'Onofrio, Edoardo Ferlazzo, Angelo Pascarella, Elena Pasini, Silvana Franceschetti, Ferruccio Panzica, Laura Canafoglia, Aglaia Vignoli, Antonietta Coppola, Valeria Badioni, Francesca Beccaria, Angelo Labate, Antonio Gambardella, Antonino Romeo, Giuseppe Capovilla, Roberto Michelucci, Pasquale Striano, Vincenzo Belcastro
Publikováno v:
Epilepsia Open, Vol 9, Iss 2, Pp 486-500 (2024)
Abstract Myoclonus classically presents as a brief (10–50 ms duration), non‐rhythmic jerk movement. The etiology could vary considerably ranging from self‐limited to chronic or even progressive disorders, the latter falling into encephalopathic
Externí odkaz:
https://doaj.org/article/e291eaca018d45fbb7678166b20955d8
Autor:
Simona Lattanzi, Nicoletta Foschi, Chiara Martellino, Daniela Audenino, Giovanni Boero, Paolo Bonanni, Edoardo Ferlazzo, Valentina Chiesa, Filippo Dainese, Marta Piccioli, Alessandra Ferrari, Angelo Labate
Publikováno v:
Neurology and Therapy, Vol 13, Iss 2, Pp 389-398 (2024)
Abstract Introduction The study aimed to evaluate the effectiveness and safety of brivaracetam (BRV) as conversion monotherapy in adults with focal epilepsy treated in the context of real-world clinical practice. Methods This was a retrospective, obs
Externí odkaz:
https://doaj.org/article/259dee47a6f44d61b496a4a84d29a018
Autor:
Sara Gasparini, Edoardo Ferlazzo, Sabrina Neri, Vittoria Cianci, Alfonso Iudice, Francesca Bisulli, Paolo Bonanni, Emanuele Caggia, Alfredo D'Aniello, Carlo Di Bonaventura, Jacopo C. DiFrancesco, Elisabetta Domina, Fedele Dono, Antonio Gambardella, Carla Marini, Alfonso Marrelli, Sara Matricardi, Alessandra Morano, Francesco Paladin, Rosaria Renna, Pasquale Striano, Angelo Pascarella, Michele Ascoli, Umberto Aguglia, PEROC Study Group
Publikováno v:
Epilepsia Open, Vol 7, Iss 4, Pp 687-696 (2022)
Abstract Objective Perampanel (PER) is indicated as adjunctive antiseizure medication (ASM) in adolescents and adults with epilepsy. Data from clinical trials show good efficacy and tolerability, while limited information is available on the routine
Externí odkaz:
https://doaj.org/article/935ccf7ad591486abdbe146b8d5d1a59
Autor:
Anna Mammì, Edoardo Ferlazzo, Sara Gasparini, Valentina Bova, Sabrina Neri, Angelo Labate, Giovanni Mastroianni, Concetta Lo Bianco, Vittoria Cianci, Umberto Aguglia
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Psychiatric and behavioural side effects are common, undesirable effects associated with antiseizure medication use. Temporal lobe epilepsy is the most common focal epilepsy in adults and it is frequently associated with drug resistance. Patients wit
Externí odkaz:
https://doaj.org/article/b089f9b2447a4da696911528f0874690
Autor:
Valeria Lucchino, Luana Scaramuzzino, Stefania Scalise, Michela Lo Conte, Clara Zannino, Giorgia Lucia Benedetto, Umberto Aguglia, Edoardo Ferlazzo, Giovanni Cuda, Elvira Immacolata Parrotta
Publikováno v:
Cells, Vol 11, Iss 21, p 3491 (2022)
Unverricht-Lundborg disease (ULD), also known as progressive myoclonic epilepsy 1 (EPM1), is a rare autosomal recessive neurodegenerative disorder characterized by a complex symptomatology that includes action- and stimulus-sensitive myoclonus and to
Externí odkaz:
https://doaj.org/article/6d6a8c7fef864716addbdb6e971790c6
Autor:
Valeria Lucchino, Luana Scaramuzzino, Stefania Scalise, Katia Grillone, Michela Lo Conte, Claudia Esposito, Umberto Aguglia, Edoardo Ferlazzo, Nicola Perrotti, Paola Malatesta, Elvira Immacolata Parrotta, Giovanni Cuda
Publikováno v:
Stem Cell Research, Vol 53, Iss , Pp 102329- (2021)
Unverricht-Lundborg disease (ULD) is an inherited form of progressive myoclonus epilepsy caused by mutations in the gene encoding Cystatin B (CSTB), an inhibitor of lysosomal proteases. The most common mutation described in ULD patients is an unstabl
Externí odkaz:
https://doaj.org/article/2cda4cafb2f6426f83e831cd6607d212
Autor:
Olimpia Musumeci, Edoardo Ferlazzo, Carmelo Rodolico, Antonio Gambardella, Monica Gagliardi, Umberto Aguglia, Antonio Toscano
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
GLUT1 Deficiency Syndrome (GLUT1-DS) is a rare and potentially treatable neurometabolic condition, caused by a reduced glucose transport into the brain and clinically characterized by an epileptic encephalopathy with movement disorders. A wide inter-
Externí odkaz:
https://doaj.org/article/787048f533584a0fa2e63de769992b65
Autor:
Antonietta Coppola, Alessia Zarabla, Andrea Maialetti, Veronica Villani, Tatiana Koudriavtseva, Emilio Russo, Agostino Nozzolillo, Chiara Sueri, Vincenzo Belcastro, Simona Balestrini, Edoardo Ferlazzo, Diana Giannarelli, Leonilda Bilo, Marta Maschio
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Background: Epilepsy is one of the most common symptoms of brain tumors. It is often drug resistant and generally worsen patients' quality of life (QoL). Brain tumors release glutamate among other mediators, contributing to seizures onset, and this i
Externí odkaz:
https://doaj.org/article/45b4c1691c2544c5b1d49ef772fe39f6
Autor:
Michele Lo Giudice, Giuseppe Varone, Cosimo Ieracitano, Nadia Mammone, Giovanbattista Gaspare Tripodi, Edoardo Ferlazzo, Sara Gasparini, Umberto Aguglia, Francesco Carlo Morabito
Publikováno v:
Entropy, Vol 24, Iss 1, p 102 (2022)
The differential diagnosis of epileptic seizures (ES) and psychogenic non-epileptic seizures (PNES) may be difficult, due to the lack of distinctive clinical features. The interictal electroencephalographic (EEG) signal may also be normal in patients
Externí odkaz:
https://doaj.org/article/c979813dbd724706a30649a87a42da0c