Clinical and neuropathological phenotype associated with the novel V189I mutation in the prion protein gene von Di Fede, Giuseppe, Catania, Marcella, Atzori, Cristiana, Moda, Fabio, Pasquali, Claudio, Indaco, Antonio, Grisoli, Marina, Zuffi, Marta, Guaita, Maria Cristina, Testi, Roberto, Taraglio, Stefano, Sessa, Maria, Gusmaroli, Graziano, Spinelli, Mariacarmela, Salzano, Giulia, Legname, Giuseppe, Tarletti, Roberto, Godi, Laura, Pocchiari, Maurizio, Tagliavini, Fabrizio, Imperiale, Daniele, Giaccone, Giorgio

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A case of acute demyelinating polyradiculoneuropathy with bilateral facial palsy after ChAdOx1 nCoV-19 vaccine von Nasuelli, Nicola Alessandro, De Marchi, Fabiola, Cecchin, Michela, De Paoli, Irene, Onorato, Susanna, Pettinaroli, Roberto, Savoini, Giovanni, Godi, Laura

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Critical illness neuro-myopathy (CINM) and focal amyotrophy in intensive care unit (ICU) patients with SARS-CoV-2: a case series von Nasuelli, Nicola Alessandro, Pettinaroli, Roberto, Godi, Laura, Savoini, Claudio, De Marchi, Fabiola, Mazzini, Letizia, Crimaldi, Federico, Pagni, Aline, Pompa, Cleta Patrizia, Colombo, Davide

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The Contribution of Vessel Wall Magnetic Resonance Imaging to the Diagnosis of Primary and Secondary Central Nervous System Vasculitis von D'Aniello, Serena, Rustici, Arianna, Gramegna, Laura Ludovica, Godi, Claudia, Piccolo, Laura, Gentile, Mauro, Zini, Andrea, Carrozzi, Alessandro, Lodi, Raffaele, Tonon, Caterina, Dall'Olio, Massimo, Simonetti, Luigi, Chieffo, Raffaella, Anzalone, Nicoletta, Cirillo, Luigi

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Long-term outcome of COVID-19 patients with acute kidney injury requiring kidney replacement therapy von Godi, Ilaria, Pasin, Laura, Ballin, Andrea, Martelli, Gabriele, Bonanno, Claudio, Terranova, Francesco, Tamburini, Enrico, Simoni, Caterina, Randon, Ginevra, Franchetti, Nicola, Cattarin, Leda, Nalesso, Federico, Calò, Lorenzo, Tiberio, Ivo

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Screening for Distress in Cancer Patients: A Multicenter, Nationwide Study in Italy von GRASSI, Luigi, JOHANSEN, Christoffer, ANNUNZIATA, Maria Antonietta, CAPOVILLA, Eleonora, COSTANTINI, Anna, GRITTI, Paolo, TORTA, Riccardo, BELLANI, Marco

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A Novel Deletion in the GH1 Gene Including the IVS3 Branch Site Responsible for Autosomal Dominant Isolated Growth Hormone Deficiency von Vivenza, Daniela, Guazzarotti, Laura, Godi, Michela, Frasca, Daniela, di Natale, Berardo, Momigliano-Richiardi, Patricia, Bona, Gianni, Giordano, Mara

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Sistema d'integració, visualització i anàlisi de dades genètiques pel seguiment de malalties minoritàries von Pol Esteve, Laura, Universitat Autònoma de Barcelona. Escola d'Enginyeria

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