Interspecific differences in the bioaccumulation of arsenic of three Patagonian top predator fish: Organ distribution and arsenic speciation von Juncos, R., Arcagni, M., Squadrone, S., Rizzo, A., Arribére, M., Barriga, J.P., Battini, M.A., Campbell, L.M., Brizio, P., Abete, M.C., Ribeiro Guevara, S.

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The importance of substrate size and interstitial space in the microhabitat selection by the stream-dwelling catfish Hatcheria macraei (Actinopterygii, Trichomycteridae) von Barriga, J. P., Espinós, N. A., Chiarello-Sosa, J. M., Battini, M. A.

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Ecological significances of ontogenetic shifts in the stream-dwelling catfish, Hatcheria macraei (Siluriformes, Trichomycteridae), in a Patagonian river von Barriga, J.P, Battini, M.A

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Annual dynamics variation of a landlocked Galaxias maculatus (Jenyns 1842) population in a Northern Patagonian river: occurrence of juvenile upstream migration von Barriga, J.P, Battini, M.A, Cussac, V.E

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Reliability of the North Star Ambulatory Assessment in a multicentric setting von Mazzone, E.S, Messina, S, Vasco, G, Main, M, Eagle, M, D’Amico, A, Doglio, L, Politano, L, Cavallaro, F, Frosini, S, Bello, L, Magri, F, Corlatti, A, Zucchini, E, Brancalion, B, Rossi, F, Ferretti, M, Motta, M.G, Cecio, M.R, Berardinelli, A, Alfieri, P, Mongini, T, Pini, A, Astrea, G, Battini, R, Comi, G, Pegoraro, E, Morandi, L, Pane, M, Angelini, C, Bruno, C, Villanova, M, Vita, G, Donati, M.A, Bertini, E, Mercuri, E

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Functional changes in Duchenne muscular dystrophy: A 12-month longitudinal cohort study von MAZZONE, E, VASCO, G, FROSINI, S, BELLO, L, BONFIGLIO, S, ZUCCHINI, E, DE SANCTIS, R, SCUTIFERO, M, BIANCO, F, ROSSI, F, MOTTA, M. C, SACCO, A, SORMANI, M. P, DONATI, M. A, MONGINI, T, PINI, A, BATTINI, R, PEGORARO, E, PANE, M, GASPERINI, S, PREVITALI, S, NAPOLITANO, S, MARTINELLI, D, TORRENTE, Y, BRUNO, C, VITA, G, COMI, G, BERTINI, E, MERCURI, E, BERARDINELLI, A, MESSINA, S, D'AMICO, A, DOGLIO, L, POLITANO, L, CAVALLARO, F

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Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling von Rice, Gillian I, del Toro Duany, Yoandris, Jenkinson, Emma M, Forte, Gabriella M A, Anderson, Beverley H, Ariaudo, Giada, Bader-Meunier, Brigitte, Baildam, Eileen M, Battini, Roberta, Beresford, Michael W, Casarano, Manuela, Chouchane, Mondher, Cimaz, Rolando, Collins, Abigail E, Cordeiro, Nuno J V, Dale, Russell C, Davidson, Joyce E, De Waele, Liesbeth, Desguerre, Isabelle, Faivre, Laurence, Fazzi, Elisa, Isidor, Bertrand, Lagae, Lieven, Latchman, Andrew R, Lebon, Pierre, Li, Chumei, Livingston, John H, Lourenço, Charles M, Mancardi, Maria Margherita, Masurel-Paulet, Alice, McInnes, Iain B, Menezes, Manoj P, Mignot, Cyril, O'Sullivan, James, Orcesi, Simona, Picco, Paolo P, Riva, Enrica, Robinson, Robert A, Rodriguez, Diana, Salvatici, Elisabetta, Scott, Christiaan, Szybowska, Marta, Tolmie, John L, Vanderver, Adeline, Vanhulle, Catherine, Vieira, Jose Pedro, Webb, Kate, Whitney, Robyn N, Williams, Simon G, Wolfe, Lynne A, Zuberi, Sameer M, Hur, Sun, Crow, Yanick J

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Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature von Rice, Gillian I, Kasher, Paul R, Forte, Gabriella M A, Mannion, Niamh M, Greenwood, Sam M, Szynkiewicz, Marcin, Dickerson, Jonathan E, Bhaskar, Sanjeev S, Zampini, Massimiliano, Briggs, Tracy A, Jenkinson, Emma M, Bacino, Carlos A, Battini, Roberta, Bertini, Enrico, Brogan, Paul A, Brueton, Louise A, Carpanelli, Marialuisa, De Laet, Corinne, de Lonlay, Pascale, del Toro, Mireia, Desguerre, Isabelle, Fazzi, Elisa, Garcia-Cazorla, Àngels, Heiberg, Arvid, Kawaguchi, Masakazu, Kumar, Ram, Lin, Jean-Pierre S-M, Lourenco, Charles M, Male, Alison M, Marques, Wilson, Mignot, Cyril, Olivieri, Ivana, Orcesi, Simona, Prabhakar, Prab, Rasmussen, Magnhild, Robinson, Robert A, Rozenberg, Flore, Schmidt, Johanna L, Steindl, Katharina, Tan, Tiong Y, van der Merwe, William G, Vanderver, Adeline, Vassallo, Grace, Wakeling, Emma L, Wassmer, Evangeline, Whittaker, Elizabeth, Livingston, John H, Lebon, Pierre, Suzuki, Tamio, McLaughlin, Paul J, Keegan, Liam P, O'Connell, Mary A, Lovell, Simon C, Crow, Yanick J

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T.P.4 von Mazzone, E.S, Pane, M, Sivo, S, Palermo, C, Sormani, M.P, Messina, S, D’Amico, A, Vita, G.L, Fanelli, L, Berardinelli, A, Donati, M.A, Baranello, G, Battini, R, Pegoraro, E, Politano, L, Bruno, C, Comi, G.P, Bertini, E, Mercuri, E

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P.2.7 6 min walk test 12 month changes in DMD: Correlation with genotype von Pane, M, Mazzone, E, Sormani, M.P, Scalise, R, Berardinelli, A, Messina, S, Torrente, Y, D’Amico, A, Doglio, L, Viggiano, E, D’Ambrosio, P, Cavallaro, F, Frosini, S, Bello, L, De Sanctis, R, Fanelli, L, Rolle, E, Bianco, F, Magri, F, Vita, G.L, Motta, M.C, Donati, M.A, Mongini, T, Pini, A, Battini, R, Pegoraro, E, Previtali, S.C, Napolitano, S, Bruno, C, Politano, L, Comi, G.P, Bertini, E, Mercuri, E

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T.P.4: Long term natural history data in ambulant boys with Duchenne muscular dystrophy: 36 month changes von Mazzone, E.S., Pane, M., Sivo, S., Palermo, C., Sormani, M.P., Messina, S., D’Amico, A., Vita, G.L., Fanelli, L., Berardinelli, A., Donati, M.A., Baranello, G., Battini, R., Pegoraro, E., Politano, L., Bruno, C., Comi, G.P., Bertini, E., Mercuri, E.

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S.P.4 Functional changes in Duchenne muscular dystrophy: A 24 month longitudinal cohort study von Mazzone, E.S, Pane, M, Scalise, R, Sormani, M.P, Torrente, Y, Berardinelli, A, Messina, S, Cavallaro, F, Amico, A. D, Doglio, L, Bruno, C, Politano, L, Frosini, S, Battini, R, Bello, L, Pegoraro, E, Bonfiglio, S, Comi, G, Pini, A, de Sanctis, R, Bianco, F, Vasco, G, Mongini, T, Donati, M.A, Previtali, S, Napolitano, S, Vita, G, Bertini, E, Mercuri, E

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Characterization of seven novel mutations in seven patients with GAMT deficiency von Item, C.B., Mercimek-Mahmutoglu, S., Battini, R., Edlinger-Horvat, C., Stromberger, C., Bodamer, O., Mühl, A., Vilaseca, M.A., Korall, H., Stöckler-Ipsiroglu, S.

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P.2.7 6min walk test 12month changes in DMD: Correlation with genotype von Pane, M., Mazzone, E., Sormani, M.P., Scalise, R., Berardinelli, A., Messina, S., Torrente, Y., D’Amico, A., Doglio, L., Viggiano, E., D’Ambrosio, P., Cavallaro, F., Frosini, S., Bello, L., De Sanctis, R., Fanelli, L., Rolle, E., Bianco, F., Magri, F., Vita, G.L., Motta, M.C., Donati, M.A., Mongini, T., Pini, A., Battini, R., Pegoraro, E., Previtali, S.C., Napolitano, S., Bruno, C., Politano, L., Comi, G.P., Bertini, E., Mercuri, E.

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S.P.4 Functional changes in Duchenne muscular dystrophy: A 24month longitudinal cohort study von Mazzone, E.S., Pane, M., Scalise, R., Sormani, M.P., Torrente, Y., Berardinelli, A., Messina, S., Cavallaro, F., ′Amico, A. D, Doglio, L., Bruno, C., Politano, L., Frosini, S., Battini, R., Bello, L., Pegoraro, E., Bonfiglio, S., Comi, G., Pini, A., de Sanctis, R., Bianco, F., Vasco, G., Mongini, T., Donati, M.A., Previtali, S., Napolitano, S., Vita, G., Bertini, E., Mercuri, E.

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Characterization of seven novel mutations in seven patients with GAMT deficiency: MUTATIONS IN BRIEF von Item, C.B., Mercimek-Mahmutoglu, S., Battini, R., Edlinger-Horvat, C., Stromberger, C., Bodamer, O., Mühl, A., Vilaseca, M.A., Korall, H., Stöckler-Ipsiroglu, S.

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