Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Valeria Fugnanesi"'
Autor:
Hannes Nordmeyer, Anna Bersano, Franco Taroni, Peter Berlit, Giuseppe Faragò, Michèle Herold, MariaRita Carriero, Agostino Parati Eugenio, Mario Savoiardo, Stefania Saccucci, Michela Morbin, Luigi Caputi, Laura Perucca, Markus Kraemer, Elisa Ciceri, Valeria Fugnanesi, Gloria Bedini, Battista Boncoraglio Giorgio
Publikováno v:
Journal of the Neurological Sciences. 364:77-83
Divry van Bogaert Syndrome (DBS) is a familial juvenile-onset disorder characterized by livedo racemosa, white matter disease, dementia, epilepsy and angiographic finding of "cerebral angiomatosis". A similar syndrome including livedo racemosa and ce
Autor:
Massimiliano Godani, Francesca Cacciatore, Sonia Spinello, Valeria Fugnanesi, Michela Morbin, Riccardo Zoia, Fabrizio Tagliavini, Giorgio Giaccone, Emanuela Maderna
Publikováno v:
Brain Pathology. 26:542-546
Tauopathies are sporadic or familial neurodegenerative diseases characterized by the accumulation of phosphorylated tau in neurons and glial cells and include encephalitis related to measles virus such as subacute sclerosing panencephalitis. We descr
Autor:
Nadia Colombo, Elena Freri, Ileana Zucca, Michela Morbin, Roberto Spreafico, Giovanni Tringali, Valentina Medici, Gloria Milesi, Laura Tassi, Manuela Bramerio, Giuseppe Didato, Valeria Fugnanesi, Francesco Cardinale, Ludovico D'Incerti, Rita Garbelli, Matteo Figini
Publikováno v:
Annals of Neurology. 79:42-58
Objective In the present report, the correlations between ex vivo high-resolution imaging and specific histological and ultrastructural patterns in type II focal cortical dysplasia (FCD) have been studied to explain the differences in the magnetic re
Autor:
A. Barbaglio, Marta Barbato, Michela Sugni, Ana R. Ribeiro, Iain C. Wilkie, Fabio Mosca, Cristiano Di Benedetto, Valeria Fugnanesi, Desirèe Dessì, Mário A. Barbosa, Francesco Bonasoro, M. Daniela Candia Carnevali, S. Tricarico, Stefano Magni
Publikováno v:
Zoology. 118:147-160
The viscoelastic properties of vertebrate connective tissues rarely undergo significant changes within physiological timescales, the only major exception being the reversible destiffening of the mammalian uterine cervix at the end of pregnancy. In co
Autor:
Vita Girgenti, Andrea Salmaggi, Chiara Vasco, Emilio Ciusani, Alessandra Canazza, Angela Maria Rizzo, Valeria Fugnanesi, Michela Morbin, Licia Rivoltini, Chiara Calatozzolo
Publikováno v:
BioMed Research International
BioMed Research International, Vol 2015 (2015)
BioMed Research International, Vol 2015 (2015)
We developed anin vitrocontact through-feet blood brain barrier (BBB) model built using type IV collagen, rat astrocytes, and human umbilical vein endothelial cells (HUVECs) cocultured through Transwell porous polycarbonate membrane. The contact betw
Autor:
Valeria Fugnanesi, Laura Cantù, Fabrizio Tagliavini, Marten Beeg, Mario Salmona, Antonio E. Elia, Davide Pareyson, Giulia Mazzoleni, Antonio Bastone, Michela Morbin, Claudia Morelli, Francesca Del Sorbo, Elena Piccoli, Vincenzo Silani, Ettore Salsano, Alessandra Erbetta, Giacomina Rossi, Simona Motta, Elena Del Favero
Publikováno v:
Neurobiology of Aging. 35:408-417
Microtubule-associated protein tau gene (MAPT) is one of the major genes linked to frontotemporal lobar degeneration, a group of neurodegenerative diseases clinically, pathologically, and genetically heterogeneous. In particular, MAPT mutations give
Autor:
Gigliola Fagiolari, Carla Giordano, Sabrina Dusi, Valeria Tiranti, Dario Brunetti, Michela Morbin, Giulia d'Amati, Costanza Lamperti, Maurizio Moggio, Valeria Fugnanesi, Silvia Marchet, Ody C. M. Sibon
Publikováno v:
Brain
Brain, 137, 57-68. Oxford University Press
Brain; Vol 137
Brain, 137, 57-68. Oxford University Press
Brain; Vol 137
Pantothenate kinase-associated neurodegeneration, caused by mutations in the PANK2 gene, is an autosomal recessive disorder characterized by dystonia, dysarthria, rigidity, pigmentary retinal degeneration and brain iron accumulation. PANK2 encodes th
Autor:
Ileana, Zucca, Gloria, Milesi, Valentina, Medici, Laura, Tassi, Giuseppe, Didato, Francesco, Cardinale, Giovanni, Tringali, Nadia, Colombo, Manuela, Bramerio, Ludovico, D'Incerti, Elena, Freri, Michela, Morbin, Valeria, Fugnanesi, Matteo, Figini, Roberto, Spreafico, Rita, Garbelli
Publikováno v:
Annals of neurology. 79(1)
In the present report, the correlations between ex vivo high-resolution imaging and specific histological and ultrastructural patterns in type II focal cortical dysplasia (FCD) have been studied to explain the differences in the magnetic resonance im
Autor:
Claudio Grassi, Michela Morbin, Valeria Fugnanesi, Roberta Fruttero, Elisabetta Marini, Mario Salmona, Antonella Federico, Sara Cocco, Laura Gasparini, Nahuai Badiola, Konstantin Chegaev, Cristian Ripoli, Antonio Bastone, Alberto Gasco, Giacomina Rossi, Barbara Rolando
Publikováno v:
Bioorganicmedicinal chemistry. 23(15)
Some symmetrical and unsymmetrical thiacarbocyanines bearing NO-donor nitrooxy and furoxan moieties were synthesized and studied as candidate anti-Alzheimer's drugs. All products activated soluble guanylate cyclase (sGC) in a dose-dependent manner, d
Autor:
Silvana Franceschetti, Federica Invernizzi, Vito Sofia, Tiziana Granata, Michela Morbin, Valeria Fugnanesi, Laura Canafoglia, Vidmer Scaioli, Isabella Gilioli, Samuel F. Berkovic, Simona Binelli, Barbara Garavaglia, Nardo Nardocci, Luisa Chiapparini
Objectives: To describe the clinical and neurophysiologic patterns of patients with neuronal ceroid lipofuscinoses associated with CLN6 mutations. Methods: We reviewed the features of 11 patients with different ages at onset. Results: Clinical diseas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4981fe74490e8ed2dd1d3c7aae3c4f10
http://hdl.handle.net/20.500.11769/45816
http://hdl.handle.net/20.500.11769/45816