Hasil Pencarian - Ronald G. Haller

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  1. 1
    Reproducibility and absolute quantification of muscle glycogen in patients with glycogen storage disease by 13C NMR spectroscopy at 7 Tesla.

    Reproducibility and absolute quantification of muscle glycogen in patients with glycogen storage disease by 13C NMR spectroscopy at 7 Tesla. oleh Katja Heinicke, Ivan E Dimitrov, Nadine Romain, Sergey Cheshkov, Jimin Ren, Craig R Malloy, Ronald G Haller

    Diterbitkan 2014-01-01
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  2. 2
    Accurate measurement of mitochondrial DNA deletion level and copy number differences in human skeletal muscle.

    Accurate measurement of mitochondrial DNA deletion level and copy number differences in human skeletal muscle. oleh John P Grady, Julie L Murphy, Emma L Blakely, Ronald G Haller, Robert W Taylor, Doug M Turnbull, Helen A L Tuppen

    Diterbitkan 2014-01-01
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  3. 3
    No effect of triheptanoin on exercise performance in McArdle disease

    No effect of triheptanoin on exercise performance in McArdle disease oleh Karen L. Madsen, Pascal Laforêt, Astrid E. Buch, Mads G. Stemmerik, Chris Ottolenghi, Stéphane N. Hatem, Daniel T. Raaschou‐Pedersen, Nanna S. Poulsen, Maria Atencio, Marie‐Pierre Luton, Alexandre Ceccaldi, Ronald G. Haller, Ros Quinlivan, Fanny Mochel, John Vissing

    Diterbitkan 2019-10-01
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  4. 4
    Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry)

    Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry) oleh Tomàs Pinós, Antoni L. Andreu, Claudio Bruno, Georgios M. Hadjigeorgiou, Ronald G. Haller, Pascal Laforêt, Alejandro Lucía, Miguel A. Martín, Andrea Martinuzzi, Carmen Navarro, Piraye Oflazer, Jean Pouget, Ros Quinlivan, Sabrina Sacconi, Renata S. Scalco, Antonio Toscano, John Vissing, Matthias Vorgerd, Andrew Wakelin, Ramon Martí, EUROMAC Consortium

    Diterbitkan 2020-10-01
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  5. 5
    OxPhos defects cause hypermetabolism and reduce lifespan in cells and in patients with mitochondrial diseases

    OxPhos defects cause hypermetabolism and reduce lifespan in cells and in patients with mitochondrial diseases oleh Gabriel Sturm, Kalpita R. Karan, Anna S. Monzel, Balaji Santhanam, Tanja Taivassalo, Céline Bris, Sarah A. Ware, Marissa Cross, Atif Towheed, Albert Higgins-Chen, Meagan J. McManus, Andres Cardenas, Jue Lin, Elissa S. Epel, Shamima Rahman, John Vissing, Bruno Grassi, Morgan Levine, Steve Horvath, Ronald G. Haller, Guy Lenaers, Douglas C. Wallace, Marie-Pierre St-Onge, Saeed Tavazoie, Vincent Procaccio, Brett A. Kaufman, Erin L. Seifert, Michio Hirano, Martin Picard

    Diterbitkan 2023-01-01
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