Water stress reveals differential antioxidant responses of tolerant and non-tolerant sugarcane genotypes von Boaretto, Luis F., Carvalho, Giselle, Borgo, Lucélia, Creste, Silvana, Landell, Marcos G.A., Mazzafera, Paulo, Azevedo, Ricardo A.

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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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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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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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proteomes of feedstocks used for the production of second‐generation ethanol: a lacuna in the biofuel era von Boaretto, L.F, Mazzafera, P

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Familial mesial temporal lobe epilepsy (FMTLE): A clinical and genetic study of 15 Italian families von Striano, P., Gambardella, A., Coppola, A., Di Bonaventura, C., Bovo, G., Diani, E., Boaretto, F., Egeo, G., Ciampa, C., Labate, A., Testoni, S., Passarelli, D., Manna, I., Sferro, C., Aguglia, U., Caranci, F., Giallonardo, A. T., Striano, S., Nobile, C., Michelucci, R.

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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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Physiological and biochemical responses of Dolichos lablab L. to cadmium support its potential as a cadmium phytoremediator von Souza, Lucas A., Piotto, Fernando A., Dourado, Manuella N., Schmidt, Daiana, Franco, Mônica R., Boaretto, Luis F., Tezotto, Tiago, Ferreira, Renato R., Azevedo, Ricardo A.

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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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Infancy onset hereditary spastic paraplegia associated with a novel atlastin mutation von Dalpozzo, F, Rossetto, M G, Boaretto, F, Sartori, E, Mostacciuolo, M L, Daga, A, Bassi, M T, Martinuzzi, A

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Activity of temozolomide (TMZ) in patients (PTS) with malignant pheochromocytoma or paraganglioma (MPP): A mono-institutional retrospective study von Lombardi, G., Ferrara, M.A., Pambuku, A., Lorusso, M., Boaretto, F., Schiavi, F., Biasini, L., Azzolin, F., Opocher, G., Zovato, S., Zagonel, V.

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The pheochromocytoma and paraganglioma syndrome: Founder effects and the PGL 1 syndrome von Opocher, G, Boaretto, F, Pignataro, V, Demattè, S, Cecchini, M.E, Erlic, Z, Schiavi, F

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Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics von Rampoldi, Luca, Caridi, Gianluca, Santon, Daniela, Boaretto, Francesca, Bernascone, Ilenia, Lamorte, Giuseppe, Tardanico, Regina, Dagnino, Monica, Colussi, Giacomo, Scolari, Francesco, Ghiggeri, Gian Marco, Amoroso, Antonio, Casari, Giorgio

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A novel missense mutation in the L1CAM gene in a boy with L1 disease von Simonati, A, Boaretto, F, Vettori, A, Dabrilli, P, Criscuolo, L, Rizzuto, N, Mostacciuolo, M L

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Quantitative in situ detection of high-risk human papillomavirus in cytological specimens by SYBR Green I fluorescent labeling von CROVELLA, S, PIRULLI, D, DE SANTO, D, DE SETA, F, BONIOTTO, M, BRAIDA, L, BOARETTO, F, GUASCHINO, S, AMOROSO, A

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A new mutation in two siblings with cystinosis presenting with Bartter syndrome von Pennesi, Marco, Marchetti, Federico, Crovella, Sergio, Boaretto, Francesca, Travan, Laura, Lazzerini, Marzia, Neri, Elena, Ventura, Alessandro

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Distal hereditary motor neuropathy (DHMN): a new locus for an autosomal recessive form von Mostacciuolo, ML, Crestanello, E, Boaretto, F, Boscolo, E, Liguori, M, Tessarolo, D, Vettori, A, Vazza, G

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Localization of a new highly repeated DNA sequence of Lemur catta (Lemuridae, Strepsirhini) von Boniotto, Michele, Ventura, Mario, Cardone, Maria Francesca, Boaretto, Francesca, Archidiacono, Nicoletta, Rocchi, Mariano, Crovella, Sergio

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The pheochromocytoma and paraganglioma syndrome: Founder effects and the PGL 1 syndrome von OPOCHER, G, BOARETTO, F, PIGNATARO, V, DEMATTE, S, CECCHINI, M. E, ERLIC, Z, SCHIAVI, F

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