Search Results - Rinchetti, P.

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  1. 1
    149VP 3D stem cell-derived spinal cord/muscle organoid model for studying and treating neuromuscular diseases

    149VP 3D stem cell-derived spinal cord/muscle organoid model for studying and treating neuromuscular diseases by Corti, S., D' Angelo, A., Beatrice, F., Ongaro, J., Rinchetti, P., Faravelli, I., Miotto, M., Lodato, S., Nizzardo, M., Comi, G., Ottoboni, L.

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    Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy

    Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy by Monfrini, Edoardo, Straniero, Letizia, Bonato, Sara, Monzio Compagnoni, Giacomo, Bordoni, Andreina, Dilena, Robertino, Rinchetti, Paola, Silipigni, Rosamaria, Ronchi, Dario, Corti, Stefania, Comi, Giacomo P., Bresolin, Nereo, Duga, Stefano, Di Fonzo, Alessio

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    Gene therapy rescues disease phenotype in a spinal muscular atrophy with respiratory distress type 1 (SMARD1) mouse model

    Gene therapy rescues disease phenotype in a spinal muscular atrophy with respiratory distress type 1 (SMARD1) mouse model by Nizzardo, Monica, Simone, Chiara, Rizzo, Federica, Salani, Sabrina, Dametti, Sara, Rinchetti, Paola, Del Bo, Roberto, Foust, Kevin, Kaspar, Brian K, Bresolin, Nereo, Comi, Giacomo P, Corti, Stefania

    Published in Science advances
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