Effects of inducers of differentiation on protein kinase C and CMP-N-acetylneuraminic acid:lactosylceramide sialyltransferase activities of HL-60 leukemia cells von Xia, X J, Gu, X B, Sartorelli, A C, Yu, R K, Santorelli, A C

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What defines mindfulness-based programs? The warp and the weft von Crane, R. S., Brewer, J., Feldman, C., Kabat-Zinn, J., Santorelli, S., Williams, J. M. G., Kuyken, W.

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Epilepsy, Behavioral Abnormalities, and Physiological Comorbidities in Syntaxin-Binding Protein 1 (STXBP1) Mutant Zebrafish von Grone, Brian P, Marchese, Maria, Hamling, Kyla R, Kumar, Maneesh G, Krasniak, Christopher S, Sicca, Federico, Santorelli, Filippo M, Patel, Manisha, Baraban, Scott C

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Implications of new physics in the decays Bc→(J/ψ, ηc)τν von Tran, C T, Ivanov, M A, Körner, J G, Santorelli, P

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The effectiveness of exercise programmes in patients with multiple myeloma: A literature review von Gan, J.H, Sim, C.Y.L, Santorelli, L.A

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Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase von Dimmock, D.P, Zhang, Q, Dionisi-Vici, C, Carrozzo, R, Shieh, J, Tang, L.Y, Truong, C, Schmitt, E, Sifry-Platt, M, Lucioli, S, Santorelli, F.M, Ficicioglu, C.H, Rodriguez, M, Wierenga, K, Enns, G.M, Longo, N, Lipson, M.H, Vallance, H, Craigen, W.J, Scaglia, F, Wong, L.J

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CLYC as a neutron detector in low background conditions von Plaza, J., Bécares, V., Cano-Ott, D., Gómez, C., Martínez, T., Mendoza, E., de Rada, A. Pérez, Pesudo, V., Sáez-Vergara, J. C., Santorelli, R., Villamarín, D., Ianni, A., Peña, C., Balibrea-Correa, J., Boeltzig, A., Imbriani, G.

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Targeting autophagy impairment improves the phenotype of a novel CLN8 zebrafish model von Marchese, Maria, Bernardi, Sara, Ogi, Asahi, Licitra, Rosario, Silvi, Giada, Mero, Serena, Galatolo, Daniele, Gammaldi, Nicola, Doccini, Stefano, Ratto, Gian Michele, Rapposelli, Simona, Neuhauss, Stephan C.F., Zang, Jingjing, Rocchiccioli, Silvia, Michelucci, Elena, Ceccherini, Elisa, Santorelli, Filippo M.

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Search for light dark matter in XENON10 data von Angle, J, Aprile, E, Arneodo, F, Baudis, L, Bernstein, A, Bolozdynya, A I, Coelho, L C C, Dahl, C E, DeViveiros, L, Ferella, A D, Fernandes, L M P, Fiorucci, S, Gaitskell, R J, Giboni, K L, Gomez, R, Hasty, R, Kastens, L, Kwong, J, Lopes, J A M, Madden, N, Manalaysay, A, Manzur, A, McKinsey, D N, Monzani, M E, Ni, K, Oberlack, U, Orboeck, J, Plante, G, Santorelli, R, dos Santos, J M F, Schulte, S, Shagin, P, Shutt, T, Sorensen, P, Winant, C, Yamashita, M

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Exclusive semileptonic decays of D and Ds mesons in the covariant confining quark model von Ivanov, M. A., Körner, J. G., Pandya, J. N., Santorelli, P., Soni, N. R., Tran, C. T.

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Maternal pre-pregnancy body mass index and risk of preterm birth: a collaboration using large routine health datasets von Cornish, R P, Magnus, M C, Urhoj, S K, Santorelli, G, Smithers, L G, Odd, D, Fraser, A, Håberg, S E, Nybo Andersen, A M, Birnie, K, Lynch, J W, Tilling, K, Lawlor, D A

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Congenital muscular dystrophies with defective glycosylation of dystroglycan: A population study von MERCURI, E, MESSINA, S, BOFFI, P, CASSANDRINI, D, LAVERDA, A, MOGGIO, M, MORANDI, L, MORONI, I, PANE, M, PEZZANI, R, PICHIECCHIO, A, PINI, A, BRUNO, C, MINETTI, C, MONGINI, T, MOTTARELLI, E, RICCI, E, RUGGIERI, A, SAREDI, S, SCUDERI, C, TESSA, A, TOSCANO, A, TORTORELLA, G, MORA, M, TREVISAN, C. P, UGGETTI, C, VASCO, G, SANTORELLI, F. M, BERTINI, E, PEGORARO, E, COMI, G. P, D'AMICO, A, AIELLO, C, BIANCHERI, R, BERARDINELLI, A

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Supratentorial and pontine MRI abnormalities characterize recessive spastic ataxia of Charlevoix-Saguenay. A comprehensive study of an Italian series von Prodi, E., Grisoli, M., Panzeri, M., Minati, L., Fattori, F., Erbetta, A., Uziel, G., D'Arrigo, S., Tessa, A., Ciano, C., Santorelli, F. M., Savoiardo, M., Mariotti, C.

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MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patients von Fiorillo, C, Astrea, G, Savarese, M, Cassandrini, D, Brisca, G, Trucco, F, Pedemonte, M, Trovato, R, Ruggiero, L, Vercelli, L, D'Amico, A, Tasca, G, Pane, M, Fanin, M, Bello, L, Broda, P, Musumeci, O, Rodolico, C, Messina, S, Vita, G L, Sframeli, M, Gibertini, S, Morandi, L, Mora, M, Maggi, L, Petrucci, A, Massa, R, Grandis, M, Toscano, A, Pegoraro, E, Mercuri, E, Bertini, E, Mongini, T, Santoro, L, Nigro, V, Minetti, C, Santorelli, F M, Bruno, C

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Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotype von Ambrosini, Elena, Sicca, Federico, Brignone, Maria S, D'Adamo, Maria C, Napolitano, Carlo, Servettini, Ilenio, Moro, Francesca, Ruan, Yanfei, Guglielmi, Luca, Pieroni, Stefania, Servillo, Giuseppe, Lanciotti, Angela, Valvo, Giulia, Catacuzzeno, Luigi, Franciolini, Fabio, Molinari, Paola, Marchese, Maria, Grottesi, Alessandro, Guerrini, Renzo, Santorelli, Filippo M, Priori, Silvia, Pessia, Mauro

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First Direct Detection Constraints on Planck-Scale Mass Dark Matter with Multiple-Scatter Signatures Using the DEAP-3600 Detector von Adhikari, P, Ajaj, R, Alpízar-Venegas, M, Auty, D J, Benmansour, H, Bina, C E, Bonivento, W, Boulay, M G, Cadeddu, M, Cai, B, Cárdenas-Montes, M, Cavuoti, S, Chen, Y, Cleveland, B T, Corning, J M, Daugherty, S, DelGobbo, P, Di Stefano, P, Doria, L, Dunford, M, Ellingwood, E, Erlandson, A, Farahani, S S, Fatemighomi, N, Fiorillo, G, Gallacher, D, García Abia, P, Garg, S, Giampa, P, Goeldi, D, Gorel, P, Graham, K, Grobov, A, Hallin, A L, Hamstra, M, Hugues, T, Ilyasov, A, Joy, A, Jigmeddorj, B, Jillings, C J, Kamaev, O, Kaur, G, Kemp, A, Kochanek, I, Kuźniak, M, Lai, M, Langrock, S, Lehnert, B, Leonhardt, A, Levashko, N, Li, X, Lissia, M, Litvinov, O, Lock, J, Longo, G, Machulin, I, McDonald, A B, McElroy, T, McLaughlin, J B, Mielnichuk, C, Mirasola, L, Monroe, J, Oliviéro, G, Pal, S, Peeters, S J M, Perry, M, Pesudo, V, Picciau, E, Piro, M-C, Pollmann, T R, Raj, N, Rand, E T, Rethmeier, C, Retière, F, Rodríguez-García, I, Roszkowski, L, Ruhland, J B, Sanchez García, E, Sánchez-Pastor, T, Santorelli, R, Seth, S, Sinclair, D, Skensved, P, Smith, B, Smith, N J T, Sonley, T, Stainforth, R, Stringer, M, Sur, B, Vázquez-Jáuregui, E, Viel, S, Walding, J, Waqar, M, Ward, M, Westerdale, S, Willis, J, Zuñiga-Reyes, A

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Dark matter results from 100 live days of XENON100 data von Aprile, E, Arisaka, K, Arneodo, F, Askin, A, Baudis, L, Behrens, A, Bokeloh, K, Brown, E, Bruch, T, Bruno, G, Cardoso, J M R, Chen, W-T, Choi, B, Cline, D, Duchovni, E, Fattori, S, Ferella, A D, Gao, F, Giboni, K-L, Gross, E, Kish, A, Lam, C W, Lamblin, J, Lang, R F, Levy, C, Lim, K E, Lin, Q, Lindemann, S, Lindner, M, Lopes, J A M, Lung, K, Undagoitia, T Marrodán, Mei, Y, Fernandez, A J Melgarejo, Ni, K, Oberlack, U, Orrigo, S E A, Pantic, E, Persiani, R, Plante, G, Ribeiro, A C C, Santorelli, R, dos Santos, J M F, Sartorelli, G, Schumann, M, Selvi, M, Shagin, P, Simgen, H, Teymourian, A, Thers, D, Vitells, O, Wang, H, Weber, M, Weinheimer, C

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LIMB-GIRDLE MUSCULAR DYSTROPHY WITH α-DYSTROGLYCAN DEFICIENCY AND MUTATIONS IN THE ISPD GENE von TASCA, G, MORO, F, AIELLO, C, CASSANDRINI, D, FIORILLO, C, BERTINI, E, BRUNO, C, SANTORELLI, F. M, RICCI, E

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Implications of new physics in the decays B c → ( J / ψ ,   η c ) τ ν von Tran, C. T., Ivanov, M. A., Körner, J. G., Santorelli, P.

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GAA-FGF14 ataxia (SCA27B): phenotypic profile, natural history progression and 4-aminopyridine treatment response von Wilke, Carlo, Pellerin, David, Mengel, David, Traschütz, Andreas, Danzi, Matt C, Dicaire, Marie-Josée, Neumann, Manuela, Lerche, Holger, Bender, Benjamin, Houlden, Henry, Züchner, Stephan, Schöls, Ludger, Brais, Bernard, Synofzik, Matthis

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