Sfoglia per Titolo
A novel multi-view image coding scheme based on view-warping and 3D-DCT
2010 Zamarin, Marco; Milani, Simone; Zanuttigh, Pietro; Cortelazzo, GUIDO MARIA
Novel multicharged silver(I)–NHC complexes derived from zwitterionic 1,3-symmetrically and 1,3-unsymmetrically substituted imidazoles and benzimidazoles: Synthesis and cytotoxic properties
2016 Marinelli, Marika; Pellei, Maura; Cimarelli, Cristina; Dias, H. V. Rasika; Marzano, Cristina; Tisato, Francesco; Porchia, Marina; Gandin, Valentina; Santini, Carlo
Novel Multifunctional Magnetic Inorganic Composites: Synthesis and Characterization
2019 Sgarbossa, Paolo; Marangoni, Giovanni; Bertani, Roberta; DEL BIANCO, Lucia; Marco, Natali; Pavarin, Daniele; Federico, Spizzo; Sergio, Tamburini
Novel Multifunctional Magnetic Inorganic Composites: Synthesis and Characterization
2019 Marangoni, Giovanni; Bertani, Roberta; DEL BIANCO, Lucia; Natali, Marco; Pavarin, Daniele; Sgarbossa, Paolo; Spizzo, Federico; Tamburini, Sergio
Novel multifunctional nanocomposites from titanate nanosheets and semiconductor quantum dots
2011 Antonello, Alessandro; Brusatin, Giovanna; Guglielmi, Massimo; Bello, Valentina; Perotto, Giovanni; Mattei, Giovanni; Maiwald, M; Zollmer, V; Chiasera, A; Ferrari, M; Martucci, Alessandro
A novel Multiplicative Polynomial Kernel for Volterra series identification
2020 Dalla, Libera; Carli, R.; Pillonetto, Gianluigi
A novel murine model for arrhythmogenic cardiomyopathy points to a pathogenic role of Wnt signaling and miRNA dysregulation.
2019 Calore, Martina; Lorenzon, Alessandra; Vitiello, Libero; Poloni, Giulia; Khan Mohsin, Af; Beffagna, Giorgia; Dazzo, Emanuela; Sacchetto, Claudia; Polishchuk, Roman; Sabatelli, Patrizia; Doliana, Roberto; Carnevale, Daniela; Lembo, Giuseppe; Bonaldo, Paolo; De Windt, Leon; Braghetta, Paola; Rampazzo, Alessandra
A novel mutation (8342G → A) in the mitochondrial tRNA(Lys) gene associated with progressive external ophthalmoplegia and myoclonus
1999 Tiranti, V.; Carrara, F.; Confalonieri, P.; Mora, M.; Maffei, R. M.; Lamantea, E.; Zeviani, M.
A novel mutation in ABCD1 unveils different clinical phenotypes in a family with adrenoleukodystrophy
2017 Margoni, M; Soli, F; Sangalli, A; Bellizzi, M; Cecchini, E; Buganza, M
A novel mutation in isoform 3 of the plasma membrane Ca2+ pump impairs cellular Ca2+ homeostasis in a patient with cerebellar ataxia and laminin subunit 1α mutations.
2015 Cali', Tito; Lopreiato, Raffaele; Shimony, J; Vineyard, M; Frizzarin, Martina; Zanni, G; Zanotti, Giuseppe; Brini, Marisa; Shinawi, M; Carafoli, Ernesto
A novel mutation in MECOM affects MPL regulation in vitro and results in thrombocytopenia and bone marrow failure
2023 Ammeti, Daniele; Marzollo, Antonio; Gabelli, Maria; Zanchetta, Melania Eva; Tretti-Parenzan, Caterina; Bottega, Roberta; Capaci, Valeria; Biffi, Alessandra; Savoia, Anna; Bresolin, Silvia; Faleschini, Michela
Novel mutation in mitochondrial Elongation Factor EF-Tu associated to dysplastic leukoencephalopathy and defective mitochondrial DNA translation
2017 Di Nottia, M.; Montanari, A.; Verrigni, D.; Oliva, R.; Torraco, A.; Fernandez-Vizarra, E.; Diodato, D.; Rizza, T.; Bianchi, M.; Catteruccia, M.; Zeviani, M.; Dionisi-Vici, C.; Francisci, S.; Bertini, E.; Carrozzo, R.
Novel mutation in mitochondrial Elongation Factor EF-Tu associated to dysplastic leukoencephalopathy and defective mitochondrial DNA translation
2017 Di Nottia, Michela; Montanari, Arianna; Verrigni, Daniela; Oliva, Romina; Torraco, Alessandra; Fernandez-Vizarra, Erika; Diodato, Daria; Rizza, Teresa; Bianchi, Marzia; Catteruccia, Michela; Zeviani, Massimo; Dionisi-Vici, Carlo; Francisci, Silvia; Bertini, Enrico; Carrozzo, Rosalba
A novel mutation in OCTN2 transporter in italian patients with primary carnitine deficiency
2002 Ceccon, M.; Mognato, Maddalena; Burighel, N.; Prandstaller, D.; Angelini, C.; Vergani, Lodovica
A novel mutation in the mitochondrial tRNA(Val) gene associated with a complex neurological presentation
1998 Tiranti, V.; D'Agruma, L.; Pareyson, D.; Mora, M.; Carrara, F.; Zelante, L.; Gasparini, P.; Zeviani, M.
A novel mutation in the mitochondrial tRNAPro gene associated with late-onset ataxia, retinitis pigmentosa, deafness, leukoencephalopathy and complex I deficiency
2009 Da Pozzo, P.; Cardaioli, E.; Malfatti, E.; Gallus, G. N.; Malandrini, A.; Gaudiano, C.; Berti, G.; Invernizzi, F.; Zeviani, M.; Federico, A.
A novel mutation in the Surf1 gene in a child with leigh disease, peripheral neuropathy, and cytochrome-c oxidase deficiency
2002 Bruno, C.; Biancheri, R.; Garavaglia, B.; Biedi, C.; Rossi, A.; Lamba, L. D.; Bado, M.; Greco, M.; Zeviani, M.; Minetti, C.
A novel mutation in the upstream open reading frame of the CDKN1B gene causes a MEN4 phenotype
2013 Occhi, Gianluca; Regazzo, Daniela; Trivellin, G; Boaretto, Francesca; Ciato, Denis; Bobisse, S; Ferasin, Sergio; Cetani, F; Pardi, E; Korbonits, M; Pellegata, Ns; Sidarovich, V; Quattrone, A; Opocher, Giuseppe; Mantero, Franco; Scaroni, Carla
A novel mutation of the EYA4 gene associated with post-lingual hearing loss in a proband is co-segregating with a novel PAX3 mutation in two congenitally deaf family members
2018 Cesca, Federica; Bettella, Elisa; Polli, Roberta; Cama, Elona; Scimemi, Pietro; Santarelli, Rosamaria; Murgia, Alessandra
Novel mutation of the mitofusin 2 gene in a family with Charcot-Marie-Tooth disease type 2 (CMT2A).
2014 Bergamin, G; Torre, Cd; Cacciavillani, M; Lucchetta, Marta; Boaretto, Francesca; Campagnolo, M; Luisa Mostacciuolo, M; Briani, Chiara
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