Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Yerma Bartolini"'
Autor:
Daniela Bartolini, Luca Mancinelli, Manila Antonelli, Maria Lia Cataldi, Marco Longoni, Yerma Bartolini, Chiara Bomprezzi, Francesca Gianno, Maria Ruggiero, Alessia Tomassini
Publikováno v:
Journal of Clinical Images and Medical Case Reports. 2
Marburg type is a rare variant of Multiple Sclerosis (MS) characterized by a severe and progressive course/evolution leading to exitus in few months. Its radiological presentation commonly raises suspicion of a malignancy, often requiring a brain bio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0aa198a53b382f758f72302403bfb66
https://doi.org/10.52768/2766-7820/1108
https://doi.org/10.52768/2766-7820/1108
Autor:
Antonino DeAngelis, Fabio Villani, Marta Velia Antonini, Edoardo Picetti, Irene Florindo, Yerma Bartolini, Laura Delaj, M.L. Caspani
Publikováno v:
Neurocritical care. 24(2)
The aim of this study was to evaluate the association between fever after the first days of ICU stay and neurological outcome after cardiac arrest (CA). We retrospectively analyzed CA patients admitted to intensive care unit (ICU). Inclusion criteria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6545abba7a03538b75138debf8577004
https://pubmed.ncbi.nlm.nih.gov/26896091
https://pubmed.ncbi.nlm.nih.gov/26896091
Autor:
Yerma Bartolini, Gabriella Egeo, Roberto Michelucci, Sandro Malacrida, Paola Banfi, Vito Sofia, Patrizia Pulitano, Salvatore Striano, Arturo de Falco, Maurizio Elia, Clementina Boniver, Pasquale Striano, Manuela Fanciulli, Carlo Di Bonaventura, Patrizia Riguzzi, Anna Teresa Giallonardo, Oriano Mecarelli, Tiziana Pisano, Angela La Neve, Emanuela Dazzo, Francesca Bisulli, Carlo Nobile, Lia Santulli, Antonio Gambardella, Marco Marchini, Simona Binelli, Patrizia Avoni, Giangennaro Coppola, Paolo Tinuper, Elena Pasini, Lilia Volpi, Fabrizio A. de Falco
SummaryPurpose In relatively small series, autosomal dominant lateral temporal epilepsy (ADLTE) has been associated with leucine-rich, glioma-inactivated 1 (LGI1) mutations in about 50% of the families, this genetic heterogeneity being probably cause
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a64ebe7bd3b84035eae5e8723be9b3a
http://hdl.handle.net/11585/173675
http://hdl.handle.net/11585/173675
Autor:
Elena Gardella, Anna Federica Marliani, Yerma Bartolini, Stefano Forlivesi, Stefano Meletti, Roberto Michelucci, Marco Giulioni, Guido Rubboli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29913f254a751ec8a3b41da15e3bb280
https://doi.org/10.1017/cbo9780511706103.015
https://doi.org/10.1017/cbo9780511706103.015