John Vissing

John Vissing

Clinical Professor

Member of:

  • Neurology


  1. 2015
  2. Published

    A New Mouse Model of Limb-Girdle Muscular Dystrophy Type 2I Homozygous for the Common L276I Mutation Mimicking the Mild Phenotype in Humans

    Krag, T. O. & Vissing, John, Dec 2015, In: Journal of Neuropathology and Experimental Neurology. 74, 12, p. 1137-46 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    Muscle imaging in patients with tubular aggregate myopathy caused by mutations in STIM1

    Tasca, G., D'Amico, A., Monforte, M., Nadaj-Pakleza, A., Vialle, M., Fattori, F., Vissing, John, Ricci, E. & Bertini, E., Nov 2015, In: Neuromuscular Disorders. 25, 11, p. 898-903 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    A third case of congenital myasthenic syndrome caused by mutations in SCN4A

    Witting, N., Werlauff, U., Ballegaard, Martin & Vissing, John, Oct 2015, p. S209-S209. 1 p.

    Research output: Contribution to conferencePosterResearchpeer-review

  5. Published

    LAMA2-related myopathy: Frequency among congenital and limb-girdle muscular dystrophies

    Løkken, N., Born, A. P., Duno, M. & Vissing, John, Oct 2015, In: Muscle & Nerve. 52, 4, p. 547-53 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    Aerobic training and postexercise protein in facioscapulohumeral muscular dystrophy: RCT study

    Andersen, G., Prahm, K. P., Dahlqvist, J. R., Citirak, G. & Vissing, John, Aug 2015, In: Neurology. 85, 5, p. 396-403 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    Lactate and Energy Metabolism During Exercise in Patients With Blocked Glycogenolysis (McArdle Disease)

    Ørngreen, M. C., Jeppesen, T. D., Taivassalo, T., Hauerslev, S., Preisler, N., Heinicke, K., Haller, R. G., Vissing, John & van Hall, Gerrit, Aug 2015, In: Journal of Clinical Endocrinology and Metabolism. 100, 8, p. E1096-E1104 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    Training improves oxidative capacity, but not function, in spinal muscular atrophy type III

    Madsen, K. L., Wils, Regitze Sølling, Preisler, N., Thøgersen, F., Berthelsen, M. P. & Vissing, John, Aug 2015, In: Muscle & Nerve. 52, 2, p. 240–244 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    Differences in genetic defects and morphology of eye- and limb muscles in mitochondrial myopathy

    Levison, L., Dunø, M., Risom, L., Toft, Peter Bjerre & Vissing, John, Jun 2015, In: Acta Ophthalmologica. 93, 4, p. e306-8

    Research output: Contribution to journalComment/debateResearchpeer-review

  10. Published

    Exercise in muscle glycogen storage diseases

    Preisler, N. R., Haller, R. G. & Vissing, John, May 2015, In: Journal of Inherited Metabolic Disease. 38, 3, p. 551-63 13 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  11. Published

    Clinical and genetic spectrum in limb-girdle muscular dystrophy type 2E

    Semplicini, C., Vissing, John, Dahlqvist, J. R., Stojkovic, T., Bello, L., Witting, N., Duno, M., Leturcq, F., Bertolin, C., D'Ambrosio, P., Eymard, B., Angelini, C., Politano, L., Laforêt, P. & Pegoraro, E., 28 Apr 2015, In: Neurology. 84, 17, p. 1772-81 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

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