Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Monica Mascaretti"'
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:
Chiara Barzaghi, Roberta Biancheri, Elisabetta Zanotto, Barbara Garavaglia, Monica Mascaretti, Daniela Rossi, Elisa De Grandis, Giovanni Morana
Publikováno v:
Braindevelopment. 34(6)
Background: Pantothenate kinase-associated neurodegeneration (PKAN) is a neurodegenerative disorder caused by pantothenate kinase (PANK2) gene mutations. Brain magnetic resonance imaging (MRI) typically shows the “eye-of-the-tiger” sign, i.e. bil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3f4f16b703d3a14ef89322eab8fb66f
https://pubmed.ncbi.nlm.nih.gov/21999968
https://pubmed.ncbi.nlm.nih.gov/21999968
Autor:
Giovanni Morana, E. De Grandis, Barbara Garavaglia, Monica Mascaretti, D. Rossi, Roberta Biancheri, Chiara Barzaghi, Elisabetta Zanotto
Publikováno v:
European Journal of Paediatric Neurology. 15:S106
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85631f6a83c5f782228735f0b8a92174
https://doi.org/10.1016/s1090-3798(11)70366-x
https://doi.org/10.1016/s1090-3798(11)70366-x
Autor:
Stefania Gimelli, Margherita Lerone, Giorgio Gimelli, Frédérique Béna, Cristina Cuoco, Monica Mascaretti, Maria Teresa Divizia, Patrizia Ronchetto, Marisol Mirabelli-Badenier
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 6, Iss 1, p 12 (2011)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background terminal deletions of the distal portion of the short arm of chromosome 3 cause a rare contiguous gene disorder characterized by growth retardation, developmental delay, mental retardation, dysmorphisms, microcephaly and ptosis. The phenot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::524f198af542cfd5e73904344a3afb75