John Vissing

John Vissing

Clinical Professor

Member of:

  • Neurology


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  1. Published

    Glycogen synthesis in glycogenin 1-deficient patients: A role for glycogenin 2 in muscle

    Krag, T. O., Ruiz-Ruiz, C. & Vissing, John, 2017, In: Journal of Clinical Endocrinology and Metabolism. 102, 8, p. 2690-2700 11 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  2. Published

    High-intensity interval training in facioscapulohumeral muscular dystrophy type 1: a randomized clinical trial

    Andersen, G., Heje, K., Buch, A. E. & Vissing, John, 2017, In: Journal of Neurology. 264, 6, p. 1099-1106

    Research output: Contribution to journal › Journal article › Research › peer-review

  3. Published

    Human growth hormone stabilizes walking and improves strength in a patient with dominantly inherited calpainopathy

    Prahm, K. P., Feldt-Rasmussen, Ulla & Vissing, John, 2017, In: Neuromuscular Disorders. 27, 4, p. 358-362

    Research output: Contribution to journal › Journal article › Research › peer-review

  4. Published

    Impaired glycogen breakdown and synthesis in phosphoglucomutase 1 deficiency

    Preisler, N., Cohen, J., Vissing, C. R., Madsen, K. L., Heinicke, K., Sharp, L. J., Phillips, L., Romain, N., Park, S. Y., Newby, M., Wyrick, P., Mancias, P., Galbo, Henrik, Vissing, John & Haller, R. G., 2017, In: Molecular Genetics and Metabolism. 122, 3, p. 117-121

    Research output: Contribution to journal › Journal article › Research › peer-review

  5. Published

    Leber hereditary optic neuropathy due to a new ND1 mutation

    Soldath, P., Wegener, Marianne, Sander, B., Rosenberg, T., Duno, M., Wibrand, F. & Vissing, John, 2017, In: Ophthalmic Genetics. 38, 5, p. 480-485 6 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  6. Published

    MRI as outcome measure in facioscapulohumeral muscular dystrophy: 1-year follow-up of 45 patients

    Andersen, G., Dahlqvist, J. R., Vissing, C. R., Heje, K., Thomsen, C. & Vissing, John, 2017, In: Journal of Neurology. 264, 3, p. 438-447

    Research output: Contribution to journal › Journal article › Research › peer-review

  7. Published

    Mitochondrial DNA mutation load in a family with the m.8344A>G point mutation and lipomas: a case study

    Jeppesen, T. D., Al-Hashimi, N., Duno, M., Wibrand, F., Andersen, G. & Vissing, John, Dec 2017, In: Clinical Case Reports. 5, 12, p. 2034-2039 6 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  8. Published

    Mitochondrial Point Mutation m.3243A>G Associates With Lower Bone Mineral Density, Thinner Cortices, and Reduced Bone Strength: A Case-Control Study

    Langdahl, J. H., Frederiksen, A. L., Hansen, S. J., Andersen, P. H., Yderstraede, K. B., Dunø, M., Vissing, John & Frost, M., 2017, In: Journal of Bone and Mineral Research. 32, 10, p. 2041-2048

    Research output: Contribution to journal › Journal article › Research › peer-review

  9. Published

    Muscle glycogen synthesis and breakdown are both impaired in glycogenin-1 deficiency

    Stemmerik, M. G., Madsen, K. L., Laforêt, P., Buch, A. E. & Vissing, John, 12 Dec 2017, In: Neurology. 89, 24, p. 2491-2494 4 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  10. Published

    PGM1 deficiency: Substrate use during exercise and effect of treatment with galactose

    Voermans, N. C., Preisler, N., Madsen, K. L., Janssen, M. C. H., Kusters, B., Abu Bakar, N., Conte, F., Lamberti, V. M. L., Nusman, F., van Engelen, B. G., van Scherpenzeel, M., Vissing, John & Lefeber, D. J., 2017, In: Neuromuscular Disorders. 27, 4, p. 370-376

    Research output: Contribution to journal › Journal article › Research › peer-review

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