John Vissing

John Vissing

Clinical Professor

Member of:

  • Neurology


  1. 2013
  2. Published

    Recurrent myoglobinuria and deranged acylcarnitines due to a mutation in the mtDNA MT-CO2 gene

    Vissing, C. R., Duno, M., Olesen, J. H., Rafiq, J., Risom, L., Christensen, E., Wibrand, F. & Vissing, John, 2013, In: Neurology. 80, 20, p. 1908-1910 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    160th ENMC International Workshop (First ENMC practical care workshop) Exercise training in patients with muscle diseases: 20-22 June 2008, Naarden, The Netherlands

    Vissing, John & van Engelen, B. G. M., 2013, In: Neuromuscular Disorders. 23, 2, p. 182-7 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    Diagnosis of Pompe disease: Muscle Biopsy vs Blood-Based Assays

    Vissing, John, Lukacs, Z. & Straub, V., 2013, In: JAMA Neurology. 70, 7, p. 923-927 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    Quantitative muscle MRI as an assessment tool for monitoring disease progression in LGMD2I: A Multicentre Longitudinal Study

    Willis, T. A., Hollingsworth, K. G., Coombs, A., Sveen, M., Andersen, S. P., Stojkovic, T., Eagle, M., Mayhew, A., de Sousa, P. L., Dewar, L., Morrow, J. M., Sinclair, C. D. J., Thornton, J. S., Bushby, K., Lochmüller, H., Hanna, M. G., Hogrel, J., Carlier, P. G., Vissing, John & Straub, V., 2013, In: P L o S One. 8, 8, p. 1-7 7 p., e70993.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    Anoctamin 5 muscular dystrophy in Denmark: prevalence, genotypes, phenotypes, cardiac findings, and muscle protein expression

    Witting, N., Duno, M., Petri, H., Krag, T., Bundgård, Henning, Køber, Lars Valeur & Vissing, John, 2013, In: Journal of Neurology. 260, 8, p. 2084-2093 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    Becker muscular dystrophy with widespread muscle hypertrophy and a non-sense mutation of exon 2

    Witting, N., Duno, M. & Vissing, John, 2013, In: Neuromuscular Disorders. 23, 1, p. 25-8 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

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