John Vissing

John Vissing

Clinical Professor

Member of:

  • Neurology


  1. 2016
  2. Published

    Muscle involvement in limb-girdle muscular dystrophy with GMPPB deficiency (LGMD2T)

    Oestergaard, S. T., Stojkovic, T., Dahlqvist, J. R., Bouchet-Seraphin, C., Nectoux, J., Leturcq, F., Cossée, M., Solé, G., Thomsen, C., Krag, T. O. & Vissing, John, Dec 2016, In: Neurology: Genetics. 2, 6, 7 p., e112.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    Towards a European Registry and Biorepository for Patients with Spinal and Bulbar Muscular Atrophy

    Pareyson, D., Fratta, P., Pradat, P., Soraru, G., Finsterer, J., Vissing, John, Jokela, M. E., Udd, B., Ludolph, A. C., Sagnelli, A. & Weydt, P., Mar 2016, In: Journal of Molecular Neuroscience. 58, 3, p. 394-400 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    Exercise Intolerance and Myoglobinuria Associated with a Novel Maternally Inherited MT-ND1 Mutation

    Rafiq, J., Duno, M., Østergaard, Elsebet, Ravn, K., Vissing, C. R., Wibrand, F. & Vissing, John, 2016, JIMD Reports. Springer, Vol. 25. p. 65-70 (JIMD Reports).

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

  5. Published

    Cytokine genes as potential biomarkers for muscle weakness in OPMD

    Riaz, M., Raz, Y., van der Slujis, B., Dickson, G., van Engelen, B., Vissing, John & Raz, V., 1 Oct 2016, In: Human Molecular Genetics. 25, 19, p. 4282-4287 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    216th ENMC international workshop: Clinical readiness in FKRP related myopathies January 15-17, 2016 Naarden, The Netherlands

    Richard, I., Laurent, J., Cirak, S., Vissing, John & ENMC FKRP Study Group, E. F. S. G., Oct 2016, In: Neuromuscular Disorders. 26, 10, p. 717-724 8 p.

    Research output: Contribution to journalComment/debateResearch

  7. Published

    Exercise training in metabolic myopathies

    Vissing, John, Oct 2016, In: Revue Neurologique. 172, 10, p. 559-565 7 p.

    Research output: Contribution to journalReviewResearchpeer-review

  8. Published

    A heterozygous 21-bp deletion in CAPN3 causes dominantly inherited limb girdle muscular dystrophy

    Vissing, John, Barresi, R., Witting, N., Van Ghelue, M., Gammelgaard, L., Bindoff, L. A., Straub, V., Lochmüller, H., Hudson, J., Arnardottir, S., Dahlbom, K., Jonsrud, C. & Duno, M., 30 Apr 2016, In: Brain. 139, 8, p. 2154-2163 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    Limb girdle muscular dystrophies: classification, clinical spectrum and emerging therapies

    Vissing, John, Oct 2016, In: Current Opinion in Neurology. 29, 5, p. 635-641 7 p.

    Research output: Contribution to journalReviewResearchpeer-review

  10. Published

    Axial myopathy: an overlooked feature of muscle diseases

    Witting, N., Andersen, L. K. & Vissing, John, 2016, In: Brain. 139, 1, p. 13-22 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  11. Published

    Prevalence and phenotypes of congenital myopathy due to α-actin 1 gene mutations

    Witting, N., Werlauff, U., Duno, M. & Vissing, John, Mar 2016, In: Muscle & Nerve. 53, 3, p. 388-93 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

ID: 915367