Zobrazeno 1 - 10
of 125
pro vyhledávání: '"Giuseppe Capovilla"'
Autor:
Alessandro Ferretti, Antonella Riva, Alice Fabrizio, Oliviero Bruni, Giuseppe Capovilla, Thomas Foiadelli, Alessandro Orsini, Umberto Raucci, Antonino Romeo, Pasquale Striano, Pasquale Parisi
Publikováno v:
Italian Journal of Pediatrics, Vol 50, Iss 1, Pp 1-12 (2024)
Abstract Febrile seizures (FS) are commonly perceived by healthcare professionals as a self-limited condition with a generally ‘benign’ nature. Nonetheless, they frequently lead to pediatric consultations, and their management can vary depending
Externí odkaz:
https://doaj.org/article/99e8e76540f44a93bb21b79f3d20833e
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:
Maria E. Sheean, Frauke Naumann-Winter, Giuseppe Capovilla, Maria Elisabeth Kalland, Eva Malikova, Segundo Mariz, Darius Matusevicius, Robert Nistico, Brigitte Schwarzer-Daum, Stelios Tsigkos, Kyriaki Tzogani, Kristina Larsson, Armando Magrelli, Violeta Stoyanova-Beninska
Publikováno v:
Frontiers in Medicine, Vol 8 (2021)
Since the implementation of the EU Orphan Regulation in 2000, the Committee for Orphan Medicinal Products at the European Medicines Agency has been evaluating the benefits of proposed orphan medicines vs. satisfactory treatment methods. This type of
Externí odkaz:
https://doaj.org/article/b2d1091cdc5d4925bfece7d576c08a3c
Autor:
Ganna Balagura, Julie Xian, Antonella Riva, Francesca Marchese, Bruria Ben Zeev, Loreto Rios, Deepa Sirsi, Patrizia Accorsi, Elisabetta Amadori, Guja Astrea, Simona Baldassari, Francesca Beccaria, Antonella Boni, Mauro Budetta, Gaetano Cantalupo, Giuseppe Capovilla, Elisabetta Cesaroni, Valentina Chiesa, Antonietta Coppola, Robertino Dilena, Raffaella Faggioli, Annarita Ferrari, Elena Fiorini, Francesca Madia, Elena Gennaro, Thea Giacomini, Lucio Giordano, Michele Iacomino, Simona Lattanzi, Carla Marini, Maria Margherita Mancardi, Massimo Mastrangelo, Tullio Messana, Carlo Minetti, Lino Nobili, Amanda Papa, Antonia Parmeggiani, Tiziana Pisano, Angelo Russo, Vincenzo Salpietro, Salvatore Savasta, Marcello Scala, Andrea Accogli, Barbara Scelsa, Paolo Scudieri, Alberto Spalice, Nicola Specchio, Marina Trivisano, Michal Tzadok, Massimiliano Valeriani, Maria Stella Vari, Alberto Verrotti, Federico Vigevano, Aglaia Vignoli, Ruud Toonen, Federico Zara, Ingo Helbig, Pasquale Striano
Publikováno v:
Balagura, G, Xian, J, Riva, A, Marchese, F, Zeev, B B, Rios, L, Sirsi, D, Accorsi, P, Amadori, E, Astrea, G, Baldassari, S, Beccaria, F, Boni, A, Budetta, M, Cantalupo, G, Capovilla, G, Cesaroni, E, Chiesa, V, Coppola, A, Dilena, R, Faggioli, R, Ferrari, A, Fiorini, E, Madia, F, Gennaro, E, Giacomini, T, Giordano, L, Iacomino, M, Lattanzi, S, Marini, C, Mancardi, M M, Mastrangelo, M, Messana, T, Minetti, C, Nobili, L, Papa, A, Parmeggiani, A, Pisano, T, Russo, A, Salpietro, V, Savasta, S, Scala, M, Accogli, A, Scelsa, B, Scudieri, P, Spalice, A, Specchio, N, Trivisano, M, Tzadok, M, Valeriani, M, Vari, M S, Verrotti, A, Vigevano, F, Vignoli, A, Toonen, R, Zara, F, Helbig, I & Striano, P 2022, ' Epilepsy Course and Developmental Trajectories in STXBP1-DEE ', Neurology: Genetics, vol. 8, no. 3, e676, pp. 1-15 . https://doi.org/10.1212/NXG.0000000000000676
Neurology: Genetics, 8(3):e676, 1-15. Lippincott Williams and Wilkins
Neurology: Genetics, 8(3):e676, 1-15. Lippincott Williams and Wilkins
Background and ObjectivesClinical manifestations in STXBP1 developmental and epileptic encephalopathy (DEE) vary in severity and outcome, and the genotypic spectrum is diverse. We aim to trace the neurodevelopmental trajectories in individuals with S
Autor:
Antonella Riva, Antonietta Coppola, Carlo Di Bonaventura, Maurizio Elia, Edoardo Ferlazzo, Giuseppe Gobbi, Carla Marini, Stefano Meletti, Antonino Romeo, Katia Santoro, Alberto Verrotti, Giuseppe Capovilla, Pasquale Striano, Umberto Aguglia, Irene Bagnasco, Emanuele Bartolini, Domenica Battaglia, Francesca Beccaria, Vincenzo Belcastro, Pia Bernardo, Paolo Bonanni, Clementina Boniver, Alice Bonuccelli, Eleonora Briatore, Francesco Brigo, Elisabetta Cesaroni, Roberta Coa, Cinzia Costa, Alfredo D'Aniello, Valentina De Giorgis, Giancarlo Di Gennaro, Anna Rita Ferrari, Francesca Marchese, Sara Matricardi, Tullio Messana, Alessandra Morano, Francesca Felicia Operto, Alessandro Orsini, Lucio Parmeggiani, Cinzia Peruzzi, Dario Pruna, Monica Puligheddu, Patrizia Pulitano, Francesca Ragona, Andrea Romigi, Anna Rosati, Eleonora Rosati, Angelo Russo, Stefano Sartori, Carlotta Spagnoli, Maria Spanò, Antonio Trabacca, Serena Troisi, Maurizio Viri, Claudio Zucca
Publikováno v:
Seizure. 101:134-140
Although international guidelines exist, the clinical heterogeneity of Lennox-Gastaut syndrome (LGS) and the increasing availability of new and repurposed drugs (e.g., fenfluramine and cannabidiol) requires a practical guide to patient management in
Autor:
Loretta Giuliano, Elisabetta Cesaroni, Alberto Verrotti, Antonella Riva, Edoardo Ferlazzo, Salvatore Striano, Antonio Gambardella, Susanna Casellato, Thomas Foiadelli, Maurizio Elia, Carlo Di Bonaventura, Vito Sofia, Giuseppe Capovilla, Teresa Di Giallonardo, Salvatore Savasta, Vincenzo Belcastro, Pasquale Striano
Publikováno v:
Seizure (Online) 93 (2021): 8–12. doi:10.1016/j.seizure.2021.09.021
info:cnr-pdr/source/autori:Belcastro V.; Casellato S.; Striano P.; Capovilla G.; Savasta S.; Foiadelli T.; Sofia V.; Giuliano L.; Riva A.; Elia M.; Cesaroni E.; Bonaventura C.D.; Giallonardo T.; Striano S.; Gambardella A.; Ferlazzo E.; Verrotti A./titolo:Epilepsy in "Sunflower syndrome": electroclinical features, therapeutic response, and long-term follow-up/doi:10.1016%2Fj.seizure.2021.09.021/rivista:Seizure (Online)/anno:2021/pagina_da:8/pagina_a:12/intervallo_pagine:8–12/volume:93
info:cnr-pdr/source/autori:Belcastro V.; Casellato S.; Striano P.; Capovilla G.; Savasta S.; Foiadelli T.; Sofia V.; Giuliano L.; Riva A.; Elia M.; Cesaroni E.; Bonaventura C.D.; Giallonardo T.; Striano S.; Gambardella A.; Ferlazzo E.; Verrotti A./titolo:Epilepsy in "Sunflower syndrome": electroclinical features, therapeutic response, and long-term follow-up/doi:10.1016%2Fj.seizure.2021.09.021/rivista:Seizure (Online)/anno:2021/pagina_da:8/pagina_a:12/intervallo_pagine:8–12/volume:93
Background Sunflower syndrome (SFS) is a rare childhood-onset generalized epilepsy characterized by photosensitivity, heliotropism, and drug-resistant stereotyped seizures maybe self-induced by hand-waving maneuvers. Data on the long-term prognosis a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b771e7aeb1775d08793238e384e9fcd9
http://hdl.handle.net/11391/1523063
http://hdl.handle.net/11391/1523063
Publikováno v:
The Importance of Photosensitivity for Epilepsy ISBN: 9783319050799
The photoparoxysmal response (PPR), also referred to as photosensitivity, is defined as the abnormal occurrence of cortical spikes or spike-and-wave discharges on EEG recording in response to intermittent photic stimulation (IPS). Rate of PPR occurre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1b131a4d3687ca8be4174d461ed1dbb
https://doi.org/10.1007/978-3-319-05080-5_6
https://doi.org/10.1007/978-3-319-05080-5_6
Autor:
Cinzia Fattore, Valentina De Giorgis, Giuseppe Capovilla, Francesca Beccaria, Valentina Franco, Paola Rota, Iolanda Mazzucchelli, Carlo Andrea Galimberti, Cecilie Johannessen Landmark, Emilio Perucca, Giuliana Gatti, Roberto Marchiselli
Publikováno v:
Epilepsia
The assay of saliva samples provides a valuable alternative to the use of blood samples for therapeutic drug monitoring (TDM), at least for certain categories of patients. To determine the feasibility of using saliva sampling for the TDM of rufinamid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e51002a45fbd7c527a7a6383937173e1
https://hdl.handle.net/10642/8797
https://hdl.handle.net/10642/8797
We would like to comment on the review article entitled “Manage- ment of status epilepticus in adults. Position paper of the Italian League against Epilepsy” [1]. This article updates the previous article published by the same Italian League agai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::038498cb9851d9f32bfbaa81c2e477ec
http://hdl.handle.net/2108/230930
http://hdl.handle.net/2108/230930