John Vissing

John Vissing

Clinical Professor

Member of:

  • Neurology


  1. 2012
  2. Published

    Change in muscle strength over time in spinal muscular atrophy types II and III. A long-term follow-up study

    Werlauff, U., Vissing, John & Steffensen, B. F., 2012, In: Neuromuscular Disorders. 22, 12, p. 1069-74 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    Endocrine function in 97 patients with myotonic dystrophy type 1

    Ørngreen, M. C., Arlien-Søborg, P., Duno, M., Hertz, J. M. & Vissing, John, 2012, In: Journal of Neurology. 259, 5, p. 912-20 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    Fat and carbohydrate metabolism during exercise in late-onset Pompe disease

    Preisler, N., Laforet, P., Madsen, K. L., Wils, Regitze Sølling, Lukacs, Z., Ørngreen, M. C., Lacour, A. & Vissing, John, 2012, In: Molecular Genetics and Metabolism. 107, 3, p. 462-8 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    Influence of erythrocyte oxygenation and intravascular ATP on resting and exercising skeletal muscle blood flow in humans with mitochondrial myopathy

    Jeppesen, T. D., Vissing, John & González-Alonso, J., 2012, In: Mitochondrion. 44, 5, p. 703-709

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    LGMD2L with bone affection: overlapping phenotype of dominant and recessive ANO5-induced disease

    Witting, N., Duno, M., Born, A. P. & Vissing, John, 2012, In: Muscle & Nerve. 46, 5, p. 829-30 2 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    Mechanisms of exertional fatigue in muscle glycogenoses

    Vissing, John & Haller, R. G., 2012, In: Neuromuscular Disorders. 22 Suppl 3, p. S168-71

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    Muscle phosphorylase kinase deficiency: a neutral metabolic variant or a disease?

    Preisler, N., Orngreen, M. C., Echaniz-Laguna, A., Laforet, P., Lonsdorfer-Wolf, E., Doutreleau, S., Geny, B., Akman, H. O., Dimauro, S. & Vissing, John, 2012, In: Neurology. 78, 4, p. 265-8 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathy

    Böhm, J., Biancalana, V., Dechene, E. T., Bitoun, M., Pierson, C. R., Schaefer, E., Karasoy, H., Dempsey, M. A., Klein, F., Dondaine, N., Kretz, C., Haumesser, N., Poirson, C., Toussaint, A., Greenleaf, R. S., Barger, M. A., Mahoney, L. J., Kang, P. B., Zanoteli, E., Vissing, J. & 48 others, Witting, N., Echaniz-Laguna, A., Wallgren-Pettersson, C., Dowling, J., Merlini, L., Oldfors, A., Bomme Ousager, L., Melki, J., Krause, A., Jern, C., Oliveira, A. S. B., Petit, F., Jacquette, A., Chaussenot, A., Mowat, D., Leheup, B., Cristofano, M., Poza Aldea, J. J., Michel, F., Furby, A., Llona, J. E. B., Van Coster, R., Bertini, E., Urtizberea, J. A., Drouin-Garraud, V., Béroud, C., Prudhon, B., Bedford, M., Mathews, K., Erby, L. A. H., Smith, S. A., Roggenbuck, J., Crowe, C. A., Brennan Spitale, A., Johal, S. C., Amato, A. A., Demmer, L. A., Jonas, J., Darras, B. T., Bird, T. D., Laurino, M., Welt, S. I., Trotter, C., Guicheney, P., Das, S., Mandel, J., Beggs, A. H. & Laporte, J., 2012, In: Human Mutation. 33, 6, p. 949-59 11 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Published

    Neuromuskulære sygdomme

    Jakobsen, J. K. & Vissing, John, 2012, Medicin. Lærebog i medicin. Baslund, B., Feldt-Rasmussen, U., Kastrup, J. & Sørensen, P. S. (eds.). p. 1099 18 p.

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

  11. 2013
  12. 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

  13. Published

    188th ENMC International Workshop: Inclusion Body Myositis, 2–4 December 2011, Naarden, The Netherlands

    Rose, M. R., Group, E. I. W. & Vissing, John, 2013, In: Neuromuscular Disorders. 23, 12, p. 1044-1055 12 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  14. Published

    A decline in PABPN1 induces progressive muscle weakness in oculopharyngeal muscle dystrophy and in muscle aging

    Anvar, S. Y., Raz, Y., Verway, N., van der Sluijs, B., Venema, A., Goeman, J. J., Vissing, John, van der Maarel, S. M., 't Hoen, P. A. C., van Engelen, B. G. M. & Raz, V., 2013, In: Aging. 5, 6, p. 412-26 15 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  15. Published

    A new mutation of the fukutin gene causing late-onset limb girdle muscular dystrophy

    Riisager, M., Duno, M., Hansen, F. J., Krag, T. O., Vissing, C. R. & Vissing, John, 2013, In: Neuromuscular Disorders. 23, 7, p. 562-567 6 p.

    Research output: Contribution to journalLetterResearchpeer-review

  16. Published

    Aerobic fitness after JDM--a long-term follow-up study

    Mathiesen, P. R., Ørngreen, M. C., Vissing, John, Andersen, L. B., Herlin, T. & Nielsen, S., 2013, In: Rheumatology. 52, 2, p. 287-95 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  17. Published

    Aerobic training in persons who have recovered from juvenile dermatomyositis

    Riisager, M., Mathiesen, P. R., Vissing, John, Preisler, N. R. & Orngreen, M. C., 2013, In: Neuromuscular Disorders. 23, 12, p. 962–968 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  18. 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

  19. 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

  20. Published

    Creatine kinase response to high-intensity aerobic exercise in adult-onset muscular dystrophy

    Andersen, S. P., Sveen, M., Wils, Regitze Sølling, Madsen, K. L., Hansen, J. B., Madsen, M. L. & Vissing, John, 2013, In: Muscle & Nerve. 48, 6, p. 897-901 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  21. 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

  22. Published

    EFNS review on the role of muscle biopsy in the investigation of myalgia

    Kyriakides, T., Angelini, C., Schaefer, J., Mongini, T., Siciliano, G., Sacconi, S., Joseph, J., Burgunder, J. M., Bindoff, L. A., Vissing, John, de Visser, M. & Hilton-Jones, D., 2013, In: European journal of neurology : the official journal of the European Federation of Neurological Societies. 20, 7, p. 997-1005 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  23. Published

    Exercise intolerance in Glycogen Storage Disease Type III: Weakness or energy deficiency?

    Preisler, N., Pradel, A., Husu, E., Madsen, K. L., Becquemin, M., Mollet, A., Labrune, P., Petit, F., Hogrel, J., Jardel, C., Maillot, F., Vissing, John & Laforêt, P., 2013, In: Molecular Genetics and Metabolism. 109, 1, p. 14-20 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  24. Published

    Fat and carbohydrate metabolism during exercise in phosphoglucomutase type 1 deficiency

    Preisler, N., Laforêt, P., Echaniz-Laguna, A., Ørngreen, M. C., Lonsdorfer-Wolf, E., Doutreleau, S., Geny, B., Stojkovic, T., Piraud, M., Petit, F. M. & Vissing, John, 2013, In: The Journal of clinical endocrinology and metabolism. 98, 7, p. E1235-E1240 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  25. Published

    Late-onset Pompe disease is prevalent in unclassified limb-girdle muscular dystrophies

    Preisler, N., Lukacs, Z., Vinge, L., Madsen, K. L., Husu, E., Wils, Regitze Sølling, Duno, M., Andersen, H., Laub, M. S. H. & Vissing, John, 2013, In: Molecular Genetics and Metabolism. 110, 3, p. 287-289 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  26. Published

    Muscle biopsies off-set normal cellular signaling in surrounding musculature

    Krag, T. O., Hauerslev, S., Dahlqvist, J. R. & Vissing, John, 2013, In: Neuromuscular Disorders. 23, 12, p. 981–985 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  27. Published

    Muscle phenotype in patients with myotonic dystrophy type 1

    Andersen, G., Orngreen, M. C., Preisler, N., Colding-Jørgensen, E., Clausen, T., Duno, M., Jeppesen, T. D. & Vissing, John, 2013, In: Muscle & Nerve.

    Research output: Contribution to journalJournal articleResearchpeer-review

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