Zobrazeno 1 - 10
of 821
pro vyhledávání: '"Licchetta A"'
Autor:
Muhammad Yasin, Laura Licchetta, Niamat Khan, Irfan Ullah, Zakir Jan, Muhammad Dawood, Asif Naveed Ahmed, Arfa Azeem, Raffaella Minardi, Valerio Carelli, Shamim Saleha
Publikováno v:
BMC Neurology, Vol 24, Iss 1, Pp 1-11 (2024)
Abstract Background Epilepsy, a challenging neurological condition, is often present with comorbidities that significantly impact diagnosis and management. In the Pakistani population, where financial limitations and geographical challenges hinder ac
Externí odkaz:
https://doaj.org/article/a6d685cf2eae43b88b7562fe7c003c6e
Autor:
Paolo Prontera, Orazio Palumbo, Massimo Carella, Corrado Zenesini, Giuseppe Damante, Laura Licchetta, Francesca Bisulli, Lorenzo Muccioli, Luca Vignatelli, Roberto Michelucci, Giuseppe D’Orsi, Elena Pasini, Maria Tappatà, Cinzia Costa, Raffaele Lodi, Serena Mazzone, Dustin Armstrong, Cosimo Altomare, Lidia Di Vito, Nicola Gambacorta, Paola Imbrici, Valentina Imperatore, Antonella Liantonio, Paola Mantuano
Publikováno v:
BMJ Open, Vol 14, Iss 10 (2024)
Introduction Lafora disease (LD) is an ultrarare fatal progressive myoclonic epilepsy, causing drug-resistant epilepsy, myoclonus and psychomotor deterioration. LD is caused by mutations in EPM2A or NHLRC1, which lead to the accumulation of polygluco
Externí odkaz:
https://doaj.org/article/9a4c3bd3835e4950ac862a864ce35aea
Autor:
Veronica Viola, Francesca Bisulli, Cesare Maria Cornaggia, Lorenzo Ferri, Laura Licchetta, Lorenzo Muccioli, Barbara Mostacci
Publikováno v:
Frontiers in Psychiatry, Vol 15 (2024)
Epileptologists and psychiatrists have long observed a correlation between epilepsy and personality disorders (PDs) in their clinical practice. We conducted a comprehensive PubMed search looking for evidence on PDs in people with epilepsy (PwE). Out
Externí odkaz:
https://doaj.org/article/bc37473c50914294a8f488229f9ce2de
Autor:
Yasin, Muhammad1 (AUTHOR), Licchetta, Laura2 (AUTHOR), Khan, Niamat1 (AUTHOR), Ullah, Irfan3 (AUTHOR), Jan, Zakir4 (AUTHOR), Dawood, Muhammad1 (AUTHOR), Ahmed, Asif Naveed1 (AUTHOR), Azeem, Arfa1 (AUTHOR), Minardi, Raffaella2 (AUTHOR), Carelli, Valerio2,5 (AUTHOR) valerio.carelli@unibo.it, Saleha, Shamim1 (AUTHOR) shamimsaleha@yahoo.com
Publikováno v:
BMC Neurology. 5/23/2024, Vol. 24 Issue 1, p1-11. 11p.
Autor:
Cancellerini, Chiara, Belotti, Laura Maria Beatrice, Mohamed, Susan, Solda', Martina, Esposito, Erika, Bisulli, Francesca, Mostacci, Barbara, Vignatelli, Luca, Tinuper, Paolo, Contin, Manuela, Licchetta, Laura
Publikováno v:
In Journal of Pharmaceutical and Biomedical Analysis 15 May 2024 242
Autor:
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
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-10 (2023)
Abstract 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 confirm
Externí odkaz:
https://doaj.org/article/a141b74afcff49a9a4cd0c5090e3921e
Autor:
Ferri, L., Menghi, V., Licchetta, L., Dimartino, P., Minardi, R., Davì, C., Di Vito, L., Cifaldi, E., Zenesini, C., Gozzo, F., Pelliccia, V., Mariani, V., de Spelorzi, Y.C.C., Gustincich, S., Seri, M., Tassi, L., Pippucci, T., Bisulli, F.
Publikováno v:
In Epilepsy & Behavior April 2024 153
Autor:
Licchetta, Laura, Bruschi, Giulia, Stipa, Carlotta, Belotti, Laura Maria Beatrice, Ferri, Lorenzo, Mostacci, Barbara, Vignatelli, Luca, Minardi, Raffaella, Di Vito, Lidia, Muccioli, Lorenzo, Boni, Antonella, Tinuper, Paolo, Bisulli, Francesca
Publikováno v:
In Epilepsy & Behavior April 2024 153
Autor:
Licchetta, Laura1 (AUTHOR) laura.licchetta@ausl.bo.it, Di Giorgi, Lucia1,2 (AUTHOR), Santucci, Margherita3 (AUTHOR), Taruffi, Lisa1 (AUTHOR), Stipa, Carlotta1 (AUTHOR), Minardi, Raffaella1 (AUTHOR), Carelli, Valerio1,3 (AUTHOR), Bisulli, Francesca1,3 (AUTHOR)
Publikováno v:
Molecular Genetics & Genomic Medicine. Jan2024, Vol. 12 Issue 1, p1-7. 7p.
Autor:
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
Publikováno v:
Epilepsia Open, Vol 7, Iss 4, Pp 810-816 (2022)
Abstract 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 perm
Externí odkaz:
https://doaj.org/article/8248074ed17846328a2bed7e16e485d0