Genetic polymorphism of NAD(P)H:quinone oxidoreductase is associated with an increased risk of infant acute lymphoblastic leukemia without MLL gene rearrangements von LANCIOTTI, M, DUFOUR, C, MICALIZZI, C, VALSECCHI, M. G, BIONDI, A, HAUPT, R, CORRAL, L, DI MICHELE, P, PIGULLO, S, DE ROSSI, G, BASSO, G, LESZL, A, LUCIANI, M, LO NIGRO, L

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Are genotypes of glutathione S-transferase superfamily a risk factor for childhood acute lymphoblastic leukemia? Results of an Italian case–control study von Pigullo, S, Haupt, R, Dufour, C, Di Michele, P, Valsecchi, M G, Basso, G, Rizzari, C, Biondi, A, Lanciotti, M

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A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effect von Di Maria, E, Gulli, R, Balestra, P, Cassandrini, D, Pigullo, S, Doria-Lamba, L, Bado, M, Schenone, A, Ajmar, F, Mandich, P, Bellone, E

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Clinical and genetic study of essential tremor in the Italian population von Abbruzzese, G, Pigullo, S, Di Maria, E, Martinelli, P, Barone, P, Marchese, R, Scaglione, C, Assini, A, Lucetti, C, Berardelli, A, Calzetti, S, Bellone, E, Ajmar, F, Mandich, P

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No evidence of association between CAG expansions and essential tremor in a large cohort of Italian patients von Pigullo, S, Di Maria, E, Marchese, R, Assini, A, Bellone, E, Scaglione, C, Vitale, C, Bonuccelli, U, Barone, P, Ajmar, F, Martinelli, P, Abbruzzese, G, Mandich, P

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Does parkin play a role in the peripheral nervous system? A family report von Abbruzzese, Giovanni, Pigullo, Simona, Schenone, Angelo, Bellone, Emilia, Marchese, Roberta, Di Maria, Emilio, Benedetti, Luana, Ciotti, Paola, Nobbio, Lucilla, Bonifati, Vincenzo, Ajmar, Franco, Mandich, Paola

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Inhibition of the M r 70,000 S6 kinase pathway by rapamycin results in chromosome malsegregation in yeast and mammalian cells von Bonatti, S., Simili, M., Galli, A., Bagnato, P., Pigullo, S., Schiestl, R. H., Abbondandolo, A.

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Essential tremor is not associated with α-synuclein gene haplotypes von Pigullo, Simona, Di Maria, Emilio, Marchese, Roberta, Bellone, Emilia, Gulli, Rossella, Scaglione, Cesa, Battaglia, Stella, Barone, Paolo, Martinelli, Paolo, Abbruzzese, Giovanni, Ajmar, Franco, Mandich, Paola

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Mutational analysis of parkin gene by denaturing high-performance liquid chromatography ( DHPLC) in essential tremor von Pigullo, Simona, De Luca, Alessandro, Barone, Paolo, Marchese, Roberta, Bellone, Emilia, Colosimo, Alessia, Scaglione, Cesa, Martinelli, Paolo, Di Maria, Emilio, Pizzuti, Antonio, Abbruzzese, Giovanni, Dallapiccola, Bruno, Ajmar, Franco, Mandich, Paola

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Glutathione S-transferase polymorphisms and susceptibility to neuroblastoma von Lanciotti, Marina, Coco, Simona, Michele, Paola Di, Haupt, Riccardo, Boni, Luca, Pigullo, Simona, Dufour, Carlo, Garaventa, Alberto, Tonini, Gian Paolo

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Genetic polymorphism of NADH:quinone oxidoreductase is associated with an increased risk of infant acute lymphoblastic leukemia without MLL gene rearrangements von Lanciotti, M, Dufour, C, Corral, L, Di Michele, P, Pigullo, S, De Rossi, G, Basso, G, Leszl, A, Luciani, M, Lo Nigro, L, Micalizzi, C, Valsecchi, M G, Biondi, A, Haupt, R

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Genetic polymorphism of NAD(P)H:quinone oxidoreductase is associated with an increased risk of infant acute lymphoblastic leukemia without MLL gene rearrangements: Infant ALL von Lanciotti, M, Dufour, C, Corral, L, Di Michele, P, Pigullo, S, De Rossi, G, Basso, G, Leszl, A, Luciani, M, Lo Nigro, L, Micalizzi, C, Valsecchi, M G, Biondi, A, Haupt, R

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Screening for mutations in the lipopolysaccharide-induced tumor necrosis factor-alpha factor (litaf) gene in italian patients with charcot-marie-tooth disease von Bellone, E, Balestra, P, Di Maria, E, Pigullo, S, Gulli, R, Ajmar, F, Mandich, P

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Induction of apoptosis and inhibition of signalling pathways by alkylated purines von Bonatti, Stefania, Pigullo, Simona, Simili, Marcella, Abbondandolo, Angelo

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A family with autosomal dominant mutilating neuropathy not linked to either Charcot–Marie–Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci von Bellone, Emilia, Rodolico, Carmelo, Toscano, Antonio, Di Maria, Emilio, Cassandrini, Denise, Pizzuti, Antonio, Pigullo, Simona, Mazzeo, Anna, Macaione, Vincenzo, Girlanda, Paolo, Vita, Giuseppe, Ajmar, Franco, Mandich, Paola

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A Family With Autosomal Dominant Mutilating Neuropathy Not Linked To Either Charcot-Marie-Tooth Disease Type 2B (CMT2B) or Hereditary Sensory Neuropathy Type I (HSN I) LOCI von Bellone, E, Rodolico, C, Toscano, A, Di Maria, E, Cassandrini, D, Pizzuti, A, Pigullo, S, Mazzeo, A, Macaione, V, Girlanda, P, Vita, G, Ajmar, F, Mandich, P.

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6DMAP inhibition of early cell cycle events and induction of mitotic abnormalities von Simili, Marcella, Pellerano, Paola, Pigullo, Simona, Tavosanis, Gaia, Ottaggio, Laura, de Saint-Georges, Louis, Bonatti, Stefania

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No evidence of association between CAG expansions and essential tremor in a large cohort of italian patients: Short communication von PIGULLO, S, DI MARIA, E, MARTINELLI, P, ABBRUZZESE, G, MANDICH, P, MARCHESE, R, ASSINI, A, BELLONE, E, SCAGLIONE, C, VITALE, C, BONUCCELLI, U, BARONE, P, AJMAR, F

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Inhibition of the Mr 70,000 S6 kinase pathway by rapamycin results in chromosome malsegregation in yeast and mammalian cells von Bonatti, S, Simili, M, Galli, A, Bagnato, P, Pigullo, S, Schiestl, R.H, Abbondandolo, A

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Exclusion of the ninjurin gene as a candidate for hereditary sensory neuropathies type I and type II von Mandich, Paola, Bellone, Emilia, Di Maria, Emilio, Pigullo, Simona, Pizzuti, Antonio, Schenone, Angelo, Soriani, Silvia, Varese, Alessandra, Windebank, Anthony J., Ajmar, Franco

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