Resultados de procura - Giulia Tozzi

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  1. 1
    Determination of Blood Total, Reduced, and Oxidized Glutathione in Pediatric Subjects

    Determination of Blood Total, Reduced, and Oxidized Glutathione in Pediatric Subjects por Anna Pastore, Fiorella Piemonte, Mattia Locatelli, Anna Lo Russo, Laura Gaeta, Giulia Tozzi, Giorgio Federici

    Publicado 2001
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  2. 2
    Glutathione imbalance in patients with X-linked adrenoleukodystrophy

    Glutathione imbalance in patients with X-linked adrenoleukodystrophy por Sara Petrillo, Fiorella Piemonte, Anna Pastore, Giulia Tozzi, Chiara Aiello, Aurora Pujol, Marco Cappa, Enrico Bertini

    Publicado 2013
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  3. 3
    Emodin Prevents Intrahepatic Fat Accumulation, Inflammation and Redox Status Imbalance During Diet-Induced Hepatosteatosis in Rats

    Emodin Prevents Intrahepatic Fat Accumulation, Inflammation and Redox Status Imbalance During Diet-Induced Hepatosteatosis in Rats por Anna Alisi, Anna Pastore, Sara Ceccarelli, Nadia Panera, Daniela Gnani, G. Bruscalupi, Mara Massimi, Giulia Tozzi, Fiorella Piemonte, Valério Nobili

    Publicado 2012
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  4. 4
    Reduced Lysosomal Acid Lipase Activity in Adult Patients With Non-alcoholic Fatty Liver Disease

    Reduced Lysosomal Acid Lipase Activity in Adult Patients With Non-alcoholic Fatty Liver Disease por Francesco Baratta, Daniele Pastori, Maria Del Ben, Licia Polimeni, Giancarlo Labbadia, Serena Di Santo, Fiorella Piemonte, Giulia Tozzi, Francesco Violi, Francesco Angelico

    Publicado 2015
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  5. 5
    Actin Glutathionylation Increases in Fibroblasts of Patients with Friedreich's Ataxia

    Actin Glutathionylation Increases in Fibroblasts of Patients with Friedreich's Ataxia por Anna Pastore, Giulia Tozzi, Laura Gaeta, Enrico Bertini, Valentina Serafini, Silvia Di Cesare, Valentina Bonetto, Filippo Casoni, Rosalba Carrozzo, Giorgio Federici, Fiorella Piemonte

    Publicado 2003
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  6. 6
    Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport

    Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport por Fátima Ferreirinha, Angelo Quattrini, Marinella Pirozzi, Valentina Valsecchi, Giorgia Dina, Vania Broccoli, Alberto Auricchio, Fiorella Piemonte, Giulia Tozzi, Laura Gaeta, Giorgio Casari, Andrea Ballabio, Elena I. Rugarli

    Publicado 2004
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  7. 7
    Lysosomal Acid Lipase as a Molecular Target of the Very Low Carbohydrate Ketogenic Diet in Morbidly Obese Patients: The Potential Effects on Liver Steatosis and Cardiovascular Risk Factors

    Lysosomal Acid Lipase as a Molecular Target of the Very Low Carbohydrate Ketogenic Diet in Morbidly Obese Patients: The Potential Effects on Liver Steatosis and Cardiovascular Risk... por Stefano Ministrini, Lucia Calzini, Elisa Nulli Migliola, Maria Anastasia Ricci, Anna Rita Roscini, Donatella Siepi, Giulia Tozzi, Giulia Daviddi, Eva-Edvige Martorelli, Maria Teresa Paganelli, Graziana Lupattelli

    Publicado 2019
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  8. 8
    Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport

    Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport por Fátima Ferreirinha, Angelo Quattrini, Marinella Pirozzi, Valentina Valsecchi, Giorgia Dina, Vania Broccoli, Alberto Auricchio, Fiorella Piemonte, Giulia Tozzi, Laura Gaeta, Giorgio Casari, Andrea Ballabio, Elena I. Rugarli

    Publicado 2004
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  9. 9
    Activation of the transcription factor EB rescues lysosomal abnormalities in cystinotic kidney cells

    Activation of the transcription factor EB rescues lysosomal abnormalities in cystinotic kidney cells por Laura Rita Rega, Elena Polishchuk, Sandro Montefusco, Gennaro Napolitano, Giulia Tozzi, Jinzhong Zhang, Francesco Bellomo, Anna Taranta, Anna Pastore, Roman Polishchuk, Fiorella Piemonte, Diego L. Medina, Sergio Catz, Andrea Ballabio, Francesco Emma

    Publicado 2016
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  10. 10
    A novel AIFM1 mutation expands the phenotype to an infantile motor neuron disease

    A novel AIFM1 mutation expands the phenotype to an infantile motor neuron disease por Daria Diodato, Giorgio Tasca, Daniela Verrigni, Adele D’Amico, Teresa Rizza, Giulia Tozzi, Diego Martinelli, Margherita Verardo, Federica Invernizzi, Alessia Nasca, Emanuele Bellacchio, Daniele Ghezzi, Fiorella Piemonte, Carlo Dionisi‐Vici, Rosalba Carrozzo, Enrico Bertini

    Publicado 2015
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