John Vissing

John Vissing

Clinical Professor

Member of:

  • Neurology


  1. 2011
  2. Published

    Clinical and molecular characterization of limb-girdle muscular dystrophy due to LAMA2 mutations

    Gavassini, B. F., Carboni, N., Nielsen, Jørgen Erik, Danielsen, E. R., Thomsen, C., Svenstrup, K., Bello, L., Maioli, M. A., Marrosu, G., Ticca, A. F., Mura, M., Marrosu, M. G., Soraru, G., Angelini, C., Vissing, John & Pegoraro, E., Nov 2011, In: Muscle & Nerve. 44, 5, p. 703-9 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    Clinical presentation and mutations in Danish patients with Wilson disease

    Møller, L. B., Horn, N., Jeppesen, T. D., Vissing, John, Wibrand, F., Jennum, Poul & Ott, P., 2011, In: European Journal of Human Genetics. 19, 9, p. 935-41 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    Deletion of exon 26 of the dystrophin gene is associated with a mild Becker muscular dystrophy phenotype

    Witting, N., Duno, M. & Vissing, John, 2011, In: Acta Myologica. 30, 3, p. 182-4 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    Deregulation of the ubiquitin-proteasome system is the predominant molecular pathology in OPMD animal models and patients

    Anvar, S. Y., hoen, P. A., Venema, A., van der Sluijs, B., van Engelen, B., Snoeck, M., Vissing, John, Trollet, C., Dickson, G., Chartier, A., Simonelig, M., van Ommen, G. B., van der Maarel, S. M. & Raz, V., 2011, In: Skeletal Muscle. 1, 1, p. 15

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    Level of muscle regeneration in limb-girdle muscular dystrophy type 2I relates to genotype and clinical severity

    Krag, T. O., Hauerslev, S., Sveen, M. L., Schwartz, M. & Vissing, John, 2011, In: Skeletal Muscle. 1, 1, p. 31

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    Physical training for McArdle disease

    Quinlivan, R., Vissing, John, Hilton-Jones, D. & Buckley, J., 2011, In: Cochrane Database of Systematic Reviews. 12, p. CD007931

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    Task force guidelines handbook: EFNS guidelines on diagnosis and management of fatty acid mitochondrial disorders.

    Angelini, C., Federico, A., Reichmann, H., Lombes, A., Vianey-Saban, C., Chinnery, P., Turnbull, D. & Vissing, John, 2011, Task force guidelines handbook.: EFNS guidelines on diagnosis and management of fatty acid mitochondrial disorders.. 2 ed. Blackwell Publishing, Vol. 1. p. 501-511

    Research output: Chapter in Book/Report/Conference proceedingBook chapterResearchpeer-review

ID: 915367