Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Luigi Sicurella"'
Autor:
Niccolò Orlandi, Giuseppe d'Orsi, Giada Pauletto, Annacarmen Nilo, Luigi Sicurella, Francesca Pescini, Francesca Giglia, Angelo Labate, Angelina Laganà, Rosaria Renna, Salvatore Maria Cavalli, Leila Zummo, Mario Coletti Moja, Catello Vollono, Annarita Sabetta, Federica Ranzato, Salvatore Zappulla, Daniela Audenino, Stefania Miniello, Peiman Nazerian, Daniela Marino, Simona Lattanzi, Marta Piccioli, Anna Estraneo, Andrea Zini, Serena Servo, Giada Giovannini, Stefano Meletti, Daria Bianchini, Sara Contardi, Alessandra Fasolino, Giulio Maria Fiore, Nicoletta Foschi, Antonello Giordano, Patrizia Laisa, Daniele Lo Coco, Simona Maccora, Adriana Magaudda, Mariangela Panebianco, Elena Merli, Giovanni Piccirillo, Matteo Pugnaghi, Lorenzo Ramacciotti, Anna Elisabetta Vaudano, Giuseppina Vitale, Anna Zaniboni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f783da69b7ca62f4cc1ace484de016e
https://hdl.handle.net/11380/1304130
https://hdl.handle.net/11380/1304130
Autor:
Lidia Urso, Luigi Sicurella, Maria Grazia Distefano, Pasquale Massimo Picone, Daniela Giacomazza, Domenico Nuzzo, Gaetano Cambula, Angela Irene Colomba
Publikováno v:
Neurological Sciences
Neurological sciences (Testo stamp.) (2022). doi:10.1007/s10072-021-05670-9
info:cnr-pdr/source/autori:Urso Lidia; Distefano Maria Grazia; Cambula Gaetano; Colomba Ale.; Nuzzo Domenico.; Picone Pasquale; Giacomazza Daniela; Sicurella Luigi/titolo:The case of encephalitis in a COVID-19 pediatric patient/doi:10.1007%2Fs10072-021-05670-9/rivista:Neurological sciences (Testo stamp.)/anno:2022/pagina_da:/pagina_a:/intervallo_pagine:/volume
Neurological sciences (Testo stamp.) (2022). doi:10.1007/s10072-021-05670-9
info:cnr-pdr/source/autori:Urso Lidia; Distefano Maria Grazia; Cambula Gaetano; Colomba Ale.; Nuzzo Domenico.; Picone Pasquale; Giacomazza Daniela; Sicurella Luigi/titolo:The case of encephalitis in a COVID-19 pediatric patient/doi:10.1007%2Fs10072-021-05670-9/rivista:Neurological sciences (Testo stamp.)/anno:2022/pagina_da:/pagina_a:/intervallo_pagine:/volume
Background: The COVID-19 pandemic, induced by the worldwide spreading of the SARS-CoV-2, is well known for its clinical picture consistent with respiratory symptoms. If pulmonary complications are the most common manifestation of the disease, neurolo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bae1d3d2c85759890fe61186387ebbb
http://europepmc.org/articles/PMC8525855
http://europepmc.org/articles/PMC8525855
Autor:
Niccolò Orlandi, Salvatore Cottone, Giulia Turchi, Daniela Audenino, Adriana Rum, Giada Giovannini, Margherita Contento, Maria Teresa Di Claudio, Peiman Nazerian, Eleonora Rosati, Luigi Sicurella, Matilde Lazzari, Davide Rodorigo, Roberto Cappellani, Rosaria Renna, Annacarmen Nilo, Anna Elisabetta Vaudano, Monica Ferlisi, Giada Pauletto, Fedele Dono, Annarita Sabetta, Tiziano Zanoni, Stefano Meletti, Salvatore M Cavalli, Valentina Tontini, Simone Beretta, Klaudio Rikani, Lidia Urso, Emanuele Bartolini, Leila Zummo, Daniele Lo Coco, Lucia Zinno, Giuseppe d'Orsi, Delia Lazzaretti, Silvia Pradella, Mario Coletti Moja, Martina Guadagni, Luigi del Gaudio, F Dainese, Lorenzo Kiferle, Gionata Strigaro, Daniela Marino, Marta Piccioli, Antonello Giordano, Francesca Pescini, Irene Florindo
Purpose to evaluate the use, effectiveness, and adverse events of intravenous brivaracetam (BRV) in status epilepticus (SE). Methods a retrospective multicentric study involving 24 Italian neurology units was performed from March 2018 to June 2020. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f24082aeceed710eec4069f73427d877
https://hdl.handle.net/11380/1236897
https://hdl.handle.net/11380/1236897
Fabry disease and multiple sclerosis misdiagnosis: the role of family history and neurological signs
Autor:
Giuseppe Cammarata, Alessandro P. Burlina, Maurizio Pieroni, Paolo Colomba, Luisa Amico, Giovanni Duro, Luigi Sicurella, Riccardo Alessandro, Carmela Zizzo, Antonello Giordano, Simone Scalia
Publikováno v:
Oncotarget
Fabry disease (FD) is an X-linked inherited lysosomal storage disorder caused by a galactosidase A (a-gal A) deficiency. Central nervous system involvement and chronic white matter lesions are observed in both FD and multiple sclerosis (MS), which ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2ecd2b1d6d4d7c10fb6687b62c67703
https://doi.org/10.18632/oncotarget.23970
https://doi.org/10.18632/oncotarget.23970
Publikováno v:
Neurol Clin Pract
Consider botulism in the differential diagnosis of Miller Fisher syndrome, the pharyngeal-cervical variant of Guillain-Barre syndrome, and myasthenia gravis, as time-dependent treatment can dramatically improve patient outcomes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7526cc6cc07707189827500dd536f4fa
https://doi.org/10.1212/cpj.0000000000000814
https://doi.org/10.1212/cpj.0000000000000814
Publikováno v:
Neurological Sciences. 34:441-444
Leptomeningeal carcinomatosis (LC) refers to diffuse seeding of the leptomeninges by tumor metastases. The clinical presentation may differ and the diagnosis may be difficult especially when cancer has not yet been diagnosed. We report a case of LC,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10d68c4878ab736266042d4ce7570e47
https://doi.org/10.1007/s10072-012-1021-1
https://doi.org/10.1007/s10072-012-1021-1
Autor:
Ines Monte, Francesco Iemolo, Carmela Zizzo, Giovanni Duro, Pasquale Fatuzzo, Riccardo Alessandro, Margherita Stefania Rodolico, Giuseppe Cammarata, Luigi Sicurella, Paolo Colomba, Caterina Bartolotta
Publikováno v:
BioMed Research International, Vol 2015 (2015)
BioMed Research International
2015 (2015): 1–5. doi:10.1155/2015/504784
info:cnr-pdr/source/autori:Cammarata G; Fatuzzo P; Rodolico MS; Colomba P; Sicurella L; Iemolo F; Zizzo C; Alessandro R; Bartolotta C; Duro G; Monte I/titolo:High variability of fabry disease manifestations in an extended italian family/doi:10.1155%2F2015%2F504784/rivista:BioMed Research International (Print)/anno:2015/pagina_da:1/pagina_a:5/intervallo_pagine:1–5/volume:2015
BioMed Research International
2015 (2015): 1–5. doi:10.1155/2015/504784
info:cnr-pdr/source/autori:Cammarata G; Fatuzzo P; Rodolico MS; Colomba P; Sicurella L; Iemolo F; Zizzo C; Alessandro R; Bartolotta C; Duro G; Monte I/titolo:High variability of fabry disease manifestations in an extended italian family/doi:10.1155%2F2015%2F504784/rivista:BioMed Research International (Print)/anno:2015/pagina_da:1/pagina_a:5/intervallo_pagine:1–5/volume:2015
Fabry disease (FD) is an inherited metabolic disorder caused by partial or full inactivation of the lysosomal hydrolaseα-galactosidase A (α-GAL). The impairment ofα-GAL results in the accumulation of undegraded glycosphingolipids in lysosomes and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5db194ecb588bc3e51485176e2890d97
https://doaj.org/article/9693dd4378194303a7d9ecb9f4e3adb1
https://doaj.org/article/9693dd4378194303a7d9ecb9f4e3adb1