Search Results - Pareyson, Daniele

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  1. 1
    Flattening and folding towels with a single-arm robot based on reinforcement learning

    Flattening and folding towels with a single-arm robot based on reinforcement learning by Shehawy, Hassan, Pareyson, Daniele, Caruso, Virginia, De Bernardi, Stefano, Zanchettin, Andrea Maria, Rocco, Paolo

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  2. 2
    The value of serum creatinine as biomarker of disease progression in spinal and bulbar muscular atrophy (SBMA)

    The value of serum creatinine as biomarker of disease progression in spinal and bulbar muscular atrophy (SBMA) by Blasi, Lorenzo, Sabbatini, Daniele, Fortuna, Andrea, Querin, Giorgia, Martinelli, Ilaria, Vianello, Sara, Bertolin, Cinzia, Pareyson, Davide, Pennuto, Maria, Pegoraro, Elena, Bello, Luca, Sorarù, Gianni

    Published in Scientific reports
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  3. 3
    Magnetic resonance neurography and diffusion tensor imaging of the sciatic nerve in hereditary transthyretin amyloidosis polyneuropathy

    Magnetic resonance neurography and diffusion tensor imaging of the sciatic nerve in hereditary transthyretin amyloidosis polyneuropathy by Gasparotti, Roberto, Salvalaggio, Alessandro, Corbo, Daniele, Agazzi, Giorgio, Cacciavillani, Mario, Lozza, Alessandro, Fenu, Silvia, De Vigili, Grazia, Tagliapietra, Matteo, Fabrizi, Gian Maria, Pareyson, Davide, Obici, Laura, Briani, Chiara

    Published in Journal of neurology
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  4. 4
    Different nerve ultrasound patterns in charcot‐marie‐tooth types and hereditary neuropathy with liability to pressure palsies

    Different nerve ultrasound patterns in charcot‐marie‐tooth types and hereditary neuropathy with liability to pressure palsies by Padua, Luca, Coraci, Daniele, Lucchetta, Marta, Paolasso, Ilaria, Pazzaglia, Costanza, Granata, Giuseppe, Cacciavillani, Mario, Luigetti, Marco, Manganelli, Fiore, Pisciotta, Chiara, Piscosquito, Giuseppe, Pareyson, Davide, Briani, Chiara

    Published in Muscle & nerve
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  5. 5
    ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy

    ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy by Caporali, Leonardo, Magri, Stefania, Legati, Andrea, Del Dotto, Valentina, Tagliavini, Francesca, Balistreri, Francesca, Nasca, Alessia, La Morgia, Chiara, Carbonelli, Michele, Valentino, Maria L., Lamantea, Eleonora, Baratta, Silvia, Schöls, Ludger, Schüle, Rebecca, Barboni, Piero, Cascavilla, Maria L., Maresca, Alessandra, Capristo, Mariantonietta, Ardissone, Anna, Pareyson, Davide, Cammarata, Gabriella, Melzi, Lisa, Zeviani, Massimo, Peverelli, Lorenzo, Lamperti, Costanza, Marzoli, Stefania B., Fang, Mingyan, Synofzik, Matthis, Ghezzi, Daniele, Carelli, Valerio, Taroni, Franco

    Published in Annals of neurology
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  6. 6
    Charcot–Marie–Tooth disease type 2F associated with biallelic HSPB1 mutations

    Charcot–Marie–Tooth disease type 2F associated with biallelic HSPB1 mutations by Abati, Elena, Magri, Stefania, Meneri, Megi, Manenti, Giulia, Velardo, Daniele, Balistreri, Francesca, Pisciotta, Chiara, Saveri, Paola, Bresolin, Nereo, Comi, Giacomo Pietro, Ronchi, Dario, Pareyson, Davide, Taroni, Franco, Corti, Stefania

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  7. 7
    Psychosocial burden and professional and social support in patients with hereditary transthyretin amyloidosis (ATTRv) and their relatives in Italy

    Psychosocial burden and professional and social support in patients with hereditary transthyretin amyloidosis (ATTRv) and their relatives in Italy by Magliano, Lorenza, Obici, Laura, Sforzini, Claudia, Mazzeo, Anna, Russo, Massimo, Cappelli, Francesco, Fenu, Silvia, Luigetti, Marco, Tagliapietra, Matteo, Gemelli, Chiara, Leonardi, Luca, Tozza, Stefano, Pradotto, Luca Guglielmo, Citarelli, Giulia, Mauro, Alessandro, Manganelli, Fiore, Antonini, Giovanni, Grandis, Marina, Fabrizi, Gian Maria, Sabatelli, Mario, Pareyson, Davide, Perfetto, Federico, Merlini, Giampaolo, Vita, Giuseppe

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  8. 8
    Virtual hospital and artificial intelligence: a first step towards the application of an innovative health system for the care of rare cerebrovascular diseases

    Virtual hospital and artificial intelligence: a first step towards the application of an innovative health system for the care of rare cerebrovascular diseases by Rifino, Nicola, Bersano, Anna, Padovani, Alessandro, Conti, Giancarlo Maria, Cavallini, Anna, Colombo, Luca, Priori, Alberto, Pianese, Raffaella, Gammone, Maria Rosaria, Erbetta, Alessandra, Ciceri, Elisa Francesca, Sattin, Davide, Varvello, Riccardo, Parati, Eugenio Agostino, Scelzo, Emma

    Published in Neurological sciences
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  9. 9
    Are novel outcome measures for Charcot–Marie–Tooth disease sensitive to change? The 6-minute walk test and StepWatch™ Activity Monitor in a 12-month longitudinal study

    Are novel outcome measures for Charcot–Marie–Tooth disease sensitive to change? The 6-minute walk test and StepWatch™ Activity Monitor in a 12-month longitudinal study by Pazzaglia, Costanza, Padua, Luca, Pareyson, Davide, Schenone, Angelo, Aiello, Alessia, Fabrizi, Gian Maria, Cavallaro, Tiziana, Santoro, Lucio, Manganelli, Fiore, Coraci, Daniele, Gemignani, Franco, Vitetta, Francesca, Quattrone, Aldo, Mazzeo, Anna, Russo, Massimo, Vita, Giuseppe

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  10. 10
    Outcome measures in the clinical evaluation of ambulatory Charcot-Marie-Tooth 1A subjects

    Outcome measures in the clinical evaluation of ambulatory Charcot-Marie-Tooth 1A subjects by Mori, Laura, Prada, Valeria, Signori, Alessio, Pareyson, Davide, Piscosquito, Giuseppe, Padua, Luca, Pazzaglia, Costanza, Fabrizi, Gian Maria, Smania, Nicola, Picelli, Alessandro, Schenone, Angelo

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  11. 11
    Charcot-Marie-Tooth disease type 2F associated with biallelic HSPB1 mutations

    Charcot-Marie-Tooth disease type 2F associated with biallelic HSPB1 mutations by Abati, Elena, Magri, Stefania, Meneri, Megi, Manenti, Giulia, Velardo, Daniele, Balistreri, Francesca, Pisciotta, Chiara, Saveri, Paola, Bresolin, Nereo, Comi, Giacomo Pietro, Ronchi, Dario, Pareyson, Davide, Taroni, Franco, Corti, Stefania

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