Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Laura Bergamino"'
Autor:
Pasquale Di Pietro, Emilio Cristina, Salvatore Renna, Andrea Rossi, Monica Mascaretti, Laura Bergamino, Antonio Piralla, Daniela Pirlo, Maria Grazia Marazzi, Milena Furione
Publikováno v:
Brain and Development. 36:70-73
Human parechoviruses (HPeVs) are a new family of neurotropic viruses that cause central nervous system (CNS) infections similar to enterovirus (EVs) meningoencephalitis in the neonatal period, resulting in white matter lesions that can be visualized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::344dc12c1fc0a0c49cd21acb5b4dac57
https://doi.org/10.1016/j.braindev.2012.12.006
https://doi.org/10.1016/j.braindev.2012.12.006
Autor:
Linda Ambrosini, Laura Bergamino, Makiko Saitoh, Angela Tacchella, Roberta Biancheri, Andrea Rossi, Masashi Mizuguchi, Valeria Capra, Marazzi Mg
Publikováno v:
Braindevelopment. 34(5)
Acute Necrotizing Encephalopathy (ANE) is a rare disorder characterized by fever, seizures and rapid progression to coma after the onset of a viral infection. Most cases are sporadic, however the observation of multiple cases in the same family with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7617beb77e5cff74e96e2725128a3dee
https://pubmed.ncbi.nlm.nih.gov/21945312
https://pubmed.ncbi.nlm.nih.gov/21945312
Autor:
Roberta Biancheri, Stefania Petrini, Carlo Minetti, Claudio Bruno, Denise Cassandrini, Adele D'Amico, Federico Zara, Mario Manfredi, Antonio Falace, Marina Pedemonte, Paolo Broda, Enrico Bertini, Filippo M. Santorelli, Laura Bergamino, Sara Scapolan, Andrea Rossi
Background Muscle-eye-brain disease is a congenital muscular dystrophy with eye and brain involvement due to POMGnT1 mutations. Objective To describe the clinical and molecular features of 3 Italian patients with POMGnT1 mutations. Design Case report
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b09f9a8ca089a1492556b7f2e36f605b
http://hdl.handle.net/11567/222350
http://hdl.handle.net/11567/222350
