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The role of clinical and neuroimaging features in the diagnosis of CADASIL

Autor: Bersano, Anna, Bedini, Gloria, Markus, Hugh Stephen, Vitali, Paolo, Colli-Tibaldi, Enrico, Taroni, Franco, Gellera, Cinzia, Baratta, Silvia, Mosca, Lorena, Carrera, Paola, Ferrari, Maurizio, Cereda, Cristina, Grieco, Gaetano, Lanfranconi, Silvia, Mazucchelli, Franca, Zarcone, Davide, De Lodovici, Maria Luisa, Bono, Giorgio, Boncoraglio, Giorgio Battista, Parati, Eugenio Agostino, Calloni, Maria Vittoria, Perrone, Patrizia, Bordo, Bianca Maria, Motto, Cristina, Agostoni, Elio, Pezzini, Alessandro, Padovani, Alessandro, Micieli, Giuseppe, Cavallini, Anna, Molini, Graziella, Sasanelli, Francesco, Sessa, Maria, Comi, Giancarlo, Checcarelli, Nicoletta, Carmerlingo, Massimo, Corato, Manuel, Marcheselli, Simona, Fusi, Laura, Grampa, Giampiero, Uccellini, Davide, Beretta, Simone, Ferrarese, Carlo, Incorvaia, Barbara, Tadeo, Carlo Sebastiano, Adobbati, Laura, Silani, Vincenzo, Faragò, Giuseppe, Trobia, Nadia, Grond-Ginsbach, Caspar, Candelise, Livia, Mazzucchelli, Franca, Guidotti, Mario, Riva, Maurizio, Iurlaro, Simona, Maria, Bianca Bordo, Braga, Massimiliano, Meola, Giovanni, Carpo, Marinella, Camerlingo, Massimo, Borutti, Giuseppina, Delodovici, Marialuisa, Verrengia, Elena Pinuccia, Tancredi, Lucia, Terruzzi, Alessandro, Magoni, Mauro, Del Zotto, Elisabetta, Bassi, Pietro, Lattuada, Patrizia, Ballabio, Elena, Gambaro, Paola, Lanfranconi, Sivia, Corrà, Barbara, Canavero, Isabella, Arbustini, Eloisa, Grasso, Maurizia, Comi, Giacomo Pietro, Corti, Stefania, Ronchi, Dario, Merlini, Giampaolo, Obici, Laura, Bassi, Maria Teresa, Tagliavini, Fabrizio, Ginsbach, Caspar Grond

BACKGROUND: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most common familial cerebral small vessel disease, caused by NOTCH3 gene mutations. The aim of our study was to identify clinical

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b9d2a995a7cde10923925259da6c29f

MM2-thalamic Creutzfeldt-Jakob disease-Neuropathological, biochemical and transmission studies identify a distinctive prion strain

Autor: Suardi, Silvia, Moda, Fabio, Di Fede, Giuseppe, Indaco, Antonio, Ruggerone, Margherita, Campagnani, Ilaria, Langeveld, Jan, Terruzzi, Alessandro, Brambilla, Antonio, Zerbi, Pietro, Fociani, Paolo, Bishop, Matthew, Will, Robert, Manson, Jean, giorgio giaccone, Tagliavini, Fabrizio

Publikováno v: Suardi, S, Moda, F, Di Fede, G, Indaco, A, Ruggerone, M, Campagnani, I, Langeveld, J, Terruzzi, A, Brambilla, A, Zerbi, P, Fociani, P, Bishop, M, Will, R, Manson, J, Giaccone, G & Tagliavini, F 2012, ' MM2-thalamic Creutzfeldt-Jakob disease-Neuropathological, biochemical and transmission studies identify a distinctive prion strain ', Prion, vol. 6, no. 4 (Suppt 1), pp. 42-43 . < http://www.landesbioscience.com/journals/prion/toc/volume/6/issue/0/ >
Web of Science

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::334d421f43dfac55f98082784a3f87d0
https://www.pure.ed.ac.uk/ws/files/13322679/MM2_thalamic_Creutzfeldt_Jakob_disease_Neuropathological_biochemical_and_transmission_studies_identify_a_distinctive_prion_strain.pdf

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Neuropathological and Biochemical Characterization of Unusual Cases of Creutzfeldt-Jakob Disease in Young, Prnp 129 mm Subjects

Autor: Moda, Fabio, giorgio giaccone, Di Fede, Giuseppe, Terruzzi, Alessandro, Suardi, Silvia, Tagliavini, Fabrizio

Publikováno v: Web of Science

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::553383e7967a1d3ab0b0d1ffdd3d1b8a
https://publons.com/wos-op/publon/12539558/