Rate dependency of β‐adrenergic modulation of repolarizing currents in the guinea‐pig ventricle von Rocchetti, M., Freli, V., Perego, V., Altomare, C., Mostacciuolo, G., Zaza, A.

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Caffeine-induced Ca(2+) signaling as an index of cardiac progenitor cells differentiation von Altomare, C, Barile, L, Marangoni, S, Rocchetti, M, Alemanni, M, Mostacciuolo, G, Giacomello, A, Messina, E, Zaza, Antonio

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Caffeine-induced Ca2+ signaling as an index of cardiac progenitor cells differentiation von Altomare, C., Barile, L., Marangoni, S., Rocchetti, M., Alemanni, M., Mostacciuolo, G., Giacomello, A., Messina, E., Zaza, Antonio

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Ca2+ handling in a guinea-pig hypertrophy/failure model von Rocchetti, M, Barassi, P, Alemanni, M, Mostacciuolo, G, Ferrari, P, Zaza, A

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Modulation of cardiac contractility by antagonism of pleckstrin-homology (PH) domain and akt-1 silencing von Chisci, R, Rocchetti, M, Menduni, F, Mostacciuolo, G, Cipolla, L, Saturno, G, Castoldi, R, Venturi, M, Zaza, A

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Rate dependency of β-adrenergic modulation of repolarizing currents in the guinea-pig ventricle von M. Rocchetti, V. Freli, V. Perego, C. Altomare, G. Mostacciuolo, A. Zaza

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Rate dependency of {szligbeta}-adrenergic modulation of repolarizing currents in the guinea-pig ventricle von Rocchetti, M, Freli, V, Perego, V, Altomare, C, Mostacciuolo, G, Zaza, A

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A voltage-dependent calcium current in mouse Swiss 3T3 fibroblasts von PERES, A, ZIPPEL, R, STURANI, E, MOSTACCIUOLO, G

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Single- and multi-channel currents recorded with patch electrodes in mouse eggs von Peres, Antonio, Mostacciuolo, Gaspare

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Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample von Mostacciuolo, ML, Pastorello, E, Vazza, G, Miorin, M, Angelini, C, Tomelleri, G, Galluzzi, G, Trevisan, CP

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High prevalence of chitotriosidase deficiency in Peruvian Amerindians exposed to chitin-bearing food and enteroparasites von Manno, N., Sherratt, S., Boaretto, F., Coico, F. Mejìa, Camus, C. Espinoza, Campos, C. Jara, Musumeci, S., Battisti, A., Quinnell, R.J., León, J. Mostacero, Vazza, G., Mostacciuolo, M.L., Paoletti, M.G., Falcone, F.H.

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SEVERE CMT TYPE 2 WITH FATAL ENCEPHALOPATHY ASSOCIATED WITH A NOVEL MFN2 SPLICING MUTATION von BOARETTO, F, VETTORI, A, MOSTACCIUOLO, M. L, MARTINUZZI, A, CASARIN, A, VAZZA, G, MUGLIA, M, ROSSETTO, M. G, CAVALLARO, T, RIZZUTO, N, CARELLI, V, SALVIATI, L

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Rare Risk Variants Identification by Identity-by-Descent Mapping and Whole-Exome Sequencing Implicates Neuronal Development Pathways in Schizophrenia and Bipolar Disorder von Salvoro, C., Bortoluzzi, S., Coppe, A., Valle, G., Feltrin, E., Mostacciuolo, M. L., Vazza, G.

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A Locus for Migraine without Aura Maps on Chromosome 14q21.2-q22.3 von Soragna, D., Vettori, A., Carraro, G., Marchioni, E., Vazza, G., Bellini, S., Tupler, R., Savoldi, F., Mostacciuolo, M.L.

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Myocardial involvement is very frequent among patients affected with subclinical Becker's muscular dystrophy von MELACINI, P, FANIN, M, ANGELINI, C, DALLA VOLTA, S, DANIELI, G. A, VILLANOVA, C, MARTINELLO, F, MIORIN, M, FREDA, M. P, MIORELLI, M, MOSTACCIUOLO, M. L, FASOLI, G

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Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum von Crimella, C, Arnoldi, A, Crippa, F, Mostacciuolo, M L, Boaretto, F, Sironi, M, D’Angelo, M Grazia, Manzoni, S, Piccinini, L, Turconi, A C, Toscano, A, Musumeci, O, Benedetti, S, Fazio, R, Bresolin, N, Daga, A, Martinuzzi, A, Bassi, M T

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A novel SACS mutation results in non-ataxic spastic paraplegia and peripheral neuropathy von Gregianin, E., Vazza, G., Scaramel, E., Boaretto, F., Vettori, A., Leonardi, E., Tosatto, S. C. E., Manara, R., Pegoraro, E., Mostacciuolo, M. L.

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A New Locus for Autosomal Recessive Spastic Paraplegia Associated with Mental Retardation and Distal Motor Neuropathy, SPG14, Maps to Chromosome 3q27-q28 von Vazza, G., Zortea, M., Boaretto, F., Micaglio, G.F., Sartori, V., Mostacciuolo, M.L.

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Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26 von Vazza, G, Bertolin, C, Scudellaro, E, Vettori, A, Boaretto, F, Rampinelli, S, De Sanctis, G, Perini, G, Peruzzi, P, Mostacciuolo, M L

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P.12.2 Dominant distal myopathy due to slow channelopathy von Angelini, C, Vazza, G, Mostacciuolo, M.L

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