Resultats de la cerca - Fabrizio Ecca

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  1. 1
    Parkinsonism after chronic exposure to the fungicide maneb (manganese ethylene-bis-dithiocarbamate).

    Parkinsonism after chronic exposure to the fungicide maneb (manganese ethylene-bis-dithiocarbamate). per G. Meco, Vincenzo Bonifati, Nicola Vanacore, Fabrizio Ecca

    Publicat 1994
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  2. 2
    Estimating the Effectiveness of DPYD Genotyping in Italian Individuals Suffering from Cancer Based on the Cost of Chemotherapy-Induced Toxicity

    Estimating the Effectiveness of DPYD Genotyping in Italian Individuals Suffering from Cancer Based on the Cost of Chemotherapy-Induced Toxicity per Vasileios Fragoulakis, Rossana Roncato, Chiara Dalle Fratte, Fabrizio Ecca, Marina Bartsakoulia, Federico Innocenti, Giuseppe Toffoli, Erika Cecchin, George P. Patrinos, Christina Mitropoulou

    Publicat 2019
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  3. 3
    Rare genetic variant burden in DPYD predicts severe fluoropyrimidine-related toxicity risk

    Rare genetic variant burden in DPYD predicts severe fluoropyrimidine-related toxicity risk per Elena De Mattia, Marco Silvestri, Jerry Polesel, Fabrizio Ecca, Silvia Mezzalira, Lucia Scarabel, Yitian Zhou, Rossana Roncato, Volker M. Lauschke, Stefano Calza, Michele Spina, Fabio Puglisi, Giuseppe Toffoli, Erika Cecchin

    Publicat 2022
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  4. 4
    A Wide Variety of Mutations in the Parkin Gene Are Responsible for Autosomal Recessive Parkinsonism in Europe

    A Wide Variety of Mutations in the Parkin Gene Are Responsible for Autosomal Recessive Parkinsonism in Europe per N. Abbas, C.B. Lücking, Sylvain Ricard, Alexandra Dürr, Vincenzo Bonifati, G. De Michele, Stephanie J. Bouley, Jenny Vaughan, Thomas Gasser, R. Marconi, E. Broussolle, Christine Brefel‐Courbon, Biswadjiet S. Harhangi, Ben A. Oostra, Fabrizio Ecca, Georg Andrees Böhme, Laurent Pradier, Nicholas Wood, Alessandro Filla, G. Meco, Patrice Denèfle, Y. Agid, Alexis Brice

    Publicat 1999
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  5. 5
    The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor

    The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor per Stefano Goldwurm, Alessio Di Fonzo, Erik Simons, C F Rohé, Michele Zini, Margherita Canesi, Silvana Tesei, Anna Zecchinelli, Angelo Antonini, Claudio Mariani, N. Meucci, Giorgio Sacilotto, Francesca Sironi, Giuliana Salani, Joaquim J. Ferreira, Hsin Fen Chien, Fabrizio Ecca, N. Vanacore, A. Dalla Libera, Fabrizio Stocchi, Cosimo Diroma, Paolo Lamberti, Cristina Andrade Sampaio, G. Meco, Egberto Reis Barbosa, Aida M. Bertoli‐Avella, Guido J. Breedveld, Ben A. Oostra, Gianni Pezzoli, Vincenzo Bonifati

    Publicat 2005
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