John Vissing

John Vissing

Clinical Professor

Member of:

  • Neurology


  1. 2022
  2. Published

    No effect of resveratrol on fatty acid oxidation or exercise capacity in patients with fatty acid oxidation disorders: A randomized clinical cross-over trial

    Storgaard, J. H., Løkken, N., Madsen, K. L., Voermans, N. C., Laforêt, P., Nadaj-Pakleza, A., Tard, C., van Hall, Gerrit, Vissing, John & Ørngreen, M. C., 2022, In: Journal of Inherited Metabolic Disease. 45, 3, p. 517-528

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    Novel truncating variants in FGD1 detected in two Danish families with Aarskog–Scott syndrome and myopathic features

    Bayat, A., Krett, B., Dunø, M., Torring, P. M. & Vissing, John, 2022, In: American Journal of Medical Genetics, Part A. 188, 7, p. 2251-2257 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    Preclinical Research in McArdle Disease: A Review of Research Models and Therapeutic Strategies

    Villarreal-Salazar, M., Brull, A., Nogales-Gadea, G., Andreu, A. L., Martín, M. A., Arenas, J., Santalla, A., Lucia, A., Vissing, John, Krag, T. O. & Pinós, T., 2022, In: Genes. 13, 1, 74.

    Research output: Contribution to journalReviewResearchpeer-review

  5. Published

    Targeted transcript analysis in muscles from patients with genetically diverse congenital myopathies

    Bachmann, C., Franchini, M., Van Den Bersselaar, L. R., Kruijt, N., Voermans, N. C., Bouman, K., Kamsteeg, E. J., Knop, K. C., Ruggiero, L., Santoro, L., Nevo, Y., Wilmshurst, J., Vissing, John, Sinnreich, M., Zorzato, D., Muntoni, F., Jungbluth, H., Zorzato, F. & Treves, S., 2022, In: Brain Communications. 4, 5, fcac224.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    Three novel FHL1 variants cause a mild phenotype of Emery-Dreifuss muscular dystrophy

    Borch, J. D. S., Krag, T., Holm-Yildiz, S. D., Cetin, H., Solheim, T. A., Fornander, F., Straub, V., Duno, M. & Vissing, John, 2022, In: Human Mutation. 43, 9, p. 1234-1238 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    β-Galactosidase deficiency in the GLB1 spectrum of lysosomal storage disease can present with severe muscle weakness and atrophy

    Pedersen, J. J., Duno, M., Wibrand, F., Hammer, C., Krag, T. & Vissing, John, 2022, In: JIMD Reports. 63, 6, p. 540-545 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. 2021
  9. Published

    Safety, efficacy, and tolerability of efgartigimod in patients with generalised myasthenia gravis (ADAPT): a multicentre, randomised, placebo-controlled, phase 3 trial

    ADAPT Investigator Study Group, A. I. S. G., Jul 2021, In: The Lancet Neurology. 20, 7, p. 526-536 11 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Published

    Efficacy and Safety of Rozanolixizumab in Moderate to Severe Generalized Myasthenia Gravis: A Phase 2 Randomized Control Trial

    MG0002 Investigators, M. I., 9 Feb 2021, In: Neurology. 96, 6, p. e853-e865 14 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  11. Published

    Episodic hyperCKaemia may be a feature of α‐methylacyl‐coenzyme A racemase deficiency

    Krett, B., Straub, V. & Vissing, John, 1 Feb 2021, In: European Journal of Neurology. 28, 2, p. 729-731 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. Published

    251st ENMC international workshop: Polyglucosan storage myopathies 13–15 December 2019, Hoofddorp, the Netherlands

    Laforêt, P., Oldfors, A., Malfatti, E., Vissing, J., Colle, M. A., Duran, J., Gentry, M., Guinovart, J., Hurley, T., Kakhlon, O., Krag, T., Landy, H., Lilleør, C. B., Minassian, B., Mingozzi, F., Murphy, E., Piercy, R., Piraud, M., Ramanan, V., Stemmerik, M. & 3 others, Thomsen, C., Weil, M. & ENMC 251st workshop study group, E. 2. W. S. G., 2021, In: Neuromuscular Disorders. 31, 5, p. 466-477 12 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

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ID: 915367