John Vissing

John Vissing

Clinical Professor

Member of:

  • Neurology


  1. 1988
  2. Published

    Effect of prior immobilization on muscular glucose clearance in resting and running rats

    Vissing, John, Ohkuwa, T., Ploug, Thorkil & Galbo, Henrik, Oct 1988, In: American Journal of Physiology (Consolidated). 255, 4 Pt 1, p. E456-62

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. 1998
  4. Published

    Sympathetic activation in exercise is not dependent on muscle acidosis: Direct evidence from studies in metabolic myopathies

    Vissing, John, Vissing, S. F., MacLean, D. A., Saltin, B., Quistorff, B. & Haller, R. G., 1998, In: Journal of Clinical Investigation. 101, p. 1654-1660

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. 2003
  6. Published

    Characterization of two new dominant ClC-1 channel mutations associated with myotonia.

    Grunnet, Morten, Jespersen, Thomas, Colding-Jørgensen, E., Schwartz, M., Klærke, Dan Arne, Vissing, John, Olesen, Søren-Peter & Dunø, M., 2003, In: Muscle & Nerve. 28, 6, p. 722-32 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. 2004
  8. Published

    Difference in allelic expression of the CLCN1 gene and the possible influence on the myotonia congenita phenotype.

    Dunø, M., Colding-Jørgensen, E., Grunnet, Morten, Jespersen, Thomas, Vissing, John & Schwartz, M., 2004, In: European Journal of Human Genetics. 12, 9, p. 738-43 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    Fuel utilization in patients with very long-chain acyl-coa dehydrogenase deficiency

    ØRngreen, M. C., Nørgaard, M., Sacchetti, M., van Engelen, B. G. M., Vissing, John & Charlot, M. G., 1 Aug 2004, In: Annals of Neurology. 56, 2, p. 279-83 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. 2005
  11. Published

    Effect of fuels on exercise capacity in muscle phosphoglycerate mutase deficiency.

    Vissing, John, Quistorff, B. & Haller, R. G., 2005, In: Archives of Neurology. 62, 9, p. 1440-3 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. 2007
  13. Published

    31P-MRS of skeletal muscle is not a sensitive diagnostic test for mitochondrial myopathy.

    Dysgaard, Tina, Quistorff, B., Wibrand, F. & Vissing, John, 2007, In: Journal of Neurology. 254, 1, p. 29-37 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  14. Published

    P-31-MRS of skeletal muscle is not a sensitive diagnostic test for mitochondrial myopathy

    Dysgaard, Tina, Quistorff, B., Wibrand, F. & Vissing, John, 2007, In: Nevrologicheskii Zhurnal. 254, 1, p. 29-37 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  15. Published

    Effects of IV glucose and oral medium-chain triglyceride in patients with VLCAD deficiency

    Ørngreen, M. C., Nørgaard, M. G., van Engelen, B. G. M., Vistisen, B., Vissing, John & Charlot, M. G., 17 Jul 2007, In: Neurology. 69, 3, p. 313-5 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  16. 2008
  17. Published

    Carbohydrate- and protein-rich diets in McArdle disease: Effects on exercise capacity

    Andersen, S. T. & Vissing, John, 2008, In: Journal of Neurology, Neurosurgery and Psychiatry. 79, 12, p. 1359-1363 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  18. Published

    Cardiac involvement in patients with limb-girdle muscular dystrophy type 2 and Becker muscular dystrophy

    Sveen, M., Thune, J. J., Køber, Lars Valeur & Vissing, John, 2008, In: Archives of Neurology. 65, 9, p. 1196-201 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  19. Published

    Effect of oral sucrose shortly before exercise on work capacity in McArdle disease

    Andersen, S. T., Haller, R. G. & Vissing, John, 2008, In: Archives of Neurology. 65, 6, p. 786-789 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  20. Published

    Endurance training improves fitness and strength in patients with Becker muscular dystrophy

    Sveen, M. L., Dysgaard, Tina, Hauerslev, S., Køber, Lars Valeur, Krag, T. O. & Vissing, John, 2008, In: Brain. 131, Pt 11, p. 2824-31 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  21. Published

    Is muscle glycogenolysis impaired in X-linked phosphorylase b kinase deficiency?

    Orngreen, M. C., Schelhaas, H. J., Jeppesen, T. D., Akman, H. O., Wevers, R. A., Andersen, S. T., Laak, H. J. T., Diggelen, O. P. V., DiMauro, S. & Vissing, John, 2008, In: Neurology. 70, 20, p. 1876-1882 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  22. Published

    No muscle involvement in myoclonus-dystonia caused by epsilon-sarcoglycan gene mutations1

    Hjermind, L. E., Vissing, John, Asmus, F., Krag, T., Lochmuller, H., Walter, M. C., Erdal, J., Blake, D. J. & Nielsen, J. E., 2008, In: European Journal of Neurology. 15, 5, p. 525-529 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  23. Published

    Open-label trial of anti-TNF-alpha in dermato- and polymyositis treated concomitantly with methotrexate

    Hengstman, G. J., Bleecker, J. L. D., Feist, E., Vissing, John, Denton, C. P., Manoussakis, M. N., Slott, J. H., Engelen, B. G. V. & Hoogen, F. H. V. D., 2008, In: European Neurology. 59, 3-4, p. 159-163 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  24. Published

    Phenotype and clinical course in a family with a new de novo Twinkle gene mutation

    Dysgaard, Tina, Schwartz, M., Colding-Jorgensen, E., Krag, T., Hauerslev, S. & Vissing, John, 2008, In: Neuromuscular Disorders. 18, 4, p. 306-309 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  25. Published

    cDNA analyses of CAPN3 enhance mutation detection and reveal a low prevalence of LGMD2A patients in Denmark

    Duno, M., Sveen, M. L., Schwartz, M. & Vissing, John, 2008, In: European Journal of Human Genetics. 16, 8, p. 935-940 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  26. 2009
  27. Published

    Drilling for energy in mitochondrial disease

    Haller, R. G. & Vissing, John, 2009, In: Archives of Neurology. 66, 8, p. 931-932 1 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  28. Published

    Effect of aerobic training in patients with spinal and bulbar muscular atrophy (Kennedy disease)

    Preisler, N., Andersen, G., Thøgersen, F., Crone, C., Dysgaard, Tina, Wibrand, F. & Vissing, John, 2009, In: Neurology. 72, 4, p. 317-23 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  29. Published

    Effect of changes in fat availability on exercise capacity in McArdle disease

    Andersen, S. T., Jeppesen, T. D., Taivassalo, T., Sveen, M. L., Heinicke, K., Haller, R. G. & Vissing, John, 2009, In: Archives of Neurology. 66, 6, p. 762-766 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  30. Published

    Glycogen branching enzyme deficiency

    Vissing, John & Lang, F., 2009, Encyclopedia of Molecular Mechanisms of Disease.. Berlin - Heidelberg: Springer, Vol. 7. p. 727-728 1 p.

    Research output: Chapter in Book/Report/Conference proceedingBook chapterResearch

  31. Published

    High prevalence of impaired glucose homeostasis and myopathy in asymptomatic and oligosymptomatic 3243A>G mitochondrial DNA mutation-positive subjects

    Frederiksen, A. L., Jeppesen, T. D., Vissing, John, Schwartz, M., Kyvik, K. O., Schmitz, O., Poulsen, P. L. & Andersen, P. H., 2009, In: Journal of Clinical Endocrinology and Metabolism. 94, 8, p. 2872-2879 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  32. Published

    High-resolution melting facilitates mutation screening of PYGM in patients with McArdle disease

    Duno, M., Quinlivan, R., Vissing, John & Schwartz, M., 2009, In: Annals of Human Genetics. 73, Pt 3, p. 292-297 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  33. Published

    Metabolic myopathies

    Vissing, John, Donato, S. D., Taroni, F., Karpati, G., Hilton-Jones, D., Bushby, K. & Griggs, R. C., 2009, Disorders of Voluntary Muscles.. 8th ed. Cambridge, UK: Cambridge University Press, Vol. 20. p. 390-407 17 p.

    Research output: Chapter in Book/Report/Conference proceedingBook chapterResearch

  34. Published

    Muscle fatigue in metabolic myopathies.

    Haller, R. G., Vissing, John, Williams, C. & Ratel, S., 2009, Human Muscle Fatigue: In Sport, Exercise and Health. London: Routledge, Vol. 12. p. 338-359 21 p.

    Research output: Chapter in Book/Report/Conference proceedingBook chapterResearch

  35. Published

    Muscle glycogenosis due to phosphoglucomutase 1 deficiency

    Stojkovic, T., Vissing, John, Petit, F., Piraud, M., Orngreen, M. C., Andersen, G., Claeys, K. G., Wary, C., Hogrel, J. & Laforêt, P., 2009, In: New England Journal of Medicine. 361, 4, p. 425-7 2 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  36. Published

    Muscle phosphoglycerate mutase deficiency revisited

    Naini, A., Toscano, A., Musumeci, O., Vissing, John, Akman, H. O. & DiMauro, S., 2009, In: Archives of Neurology. 66, 3, p. 394-8 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  37. Published

    Myoglobinuria

    Vissing, John, Lisak, R. P., Truong, D. D., Carroll, W. & Bhidayasiri, R., 2009, International Neurology: A Clinical Approach. 1st ed. Oxford, UK: Wiley-Blackwell, Vol. 125. p. 477-479 2 p.

    Research output: Chapter in Book/Report/Conference proceedingBook chapterResearch

  38. Published

    Neurologi.

    Waldemar, Gunhild, Boysen, G. M., Høgenhaven, H., Knudsen, G. M., Krarup, Christian, Olesen, Jes, Paulson, O. B., Sørensen, P. S., Vissing, John, Muckadell, O. B. S. D., Haunsø, S. & Vilstrup, H., 2009, Medicinsk Kompendium. 17th ed. København: Nyt Nordisk Forlag Arnold Busck, p. 2418-2623 205 p.

    Research output: Chapter in Book/Report/Conference proceedingBook chapterResearch

  39. Published

    Sequence variants in SPAST, SPG3A and HSPD1 in hereditary spastic paraplegia

    Svenstrup, K., Bross, P., Koefoed, P., Hjermind, L. E., Eiberg, H., Born, A. P., Vissing, J., Gyllenborg, J., Nørremølle, A., Hasholt, L., Nielsen, J. E., Svenstrup, K., Bross, P., Koefoed, P., Hjermind, L. E., Eiberg, H., Born, A. P., Vissing, J., Gyllenborg, J., Nørremølle, A. & 2 others, Hasholt, L. & Nielsen, J. E., 2009, In: Journal of the Neurological Sciences. 284, 1-2, p. 90-5 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  40. Published

    Short- and long-term effects of endurance training in patients with mitochondrial myopathy

    Jeppesen, T. D., Dunø, M., Schwartz, M., Krag, T., Rafiq, J., Wibrand, F. & Vissing, John, 2009, In: European Journal of Neurology. 16, 12, p. 1336-9 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  41. Published

    Splice mutations preserve myophosphorylase activity that ameliorates the phenotype in McArdle disease

    Vissing, John, Duno, M., Schwartz, M. & Haller, R. G., 2009, In: Brain. 132, Pt 6, p. 1545-52 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  42. 2010
  43. Published

    Arvelige neurometaboliske sygdomme

    Skovby, F. & Vissing, John, 2010, Klinisk neurologi og neurokirurgi. Gjerris, F., Paulson, O. B. & Sørensen, P. S. (eds.). 5 ed. p. 555-564 10 p.

    Research output: Chapter in Book/Report/Conference proceedingBook chapterEducation

  44. Published

    Defekter i den neuromuskulære transmission.

    Vissing, John & Paulson, O. B., 2010, Klinisk neurologi og neurokirurgi. 5 ed. København, p. 615-621 6 p.

    Research output: Chapter in Book/Report/Conference proceedingBook chapterEducation

  45. Published

    Muskelsygdomme

    Vissing, John & Sørensen, Per Soelberg, 2010, Klinisk Neurologi og Neurokirurgi. 5 ed. København, p. 623-638

    Research output: Chapter in Book/Report/Conference proceedingBook chapterEducation

  46. Published

    Myositis in Griscelli syndrome type 2 treated with hematopoietic cell transplantation

    Born, A. P., Müller, K., Marquart, Hanne Vibeke Hansen, Heilmann, C., Schejbel, L. & Vissing, John, 1 Feb 2010, In: Neuromuscular Disorders. 20, 2, p. 136-8 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  47. Published

    162nd ENMC International Workshop: Disorders of muscle lipid metabolism in adults 28-30 November 2008, Bussum, The Netherlands

    Laforêt, P., Vianey-Saban, C. & Vissing, John, 1 Apr 2010, In: Neuromuscular Disorders. 20, 4, p. 283-9 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  48. Published

    Limited diagnostic value of enzyme analysis in patients with mitochondrial tRNA mutations

    Wibrand, F., Dysgaard, Tina, Frederiksen, A. L., Olsen, D. H., Dunø, M., Schwartz, M. & Vissing, John, 1 May 2010, In: Muscle & Nerve. 41, 5, p. 607-13 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  49. Published

    McArdle disease: a clinical review

    Quinlivan, R., Buckley, J., James, M., Twist, A., Ball, S., Dunø, M., Vissing, John, Bruno, C., Cassandrini, D., Roberts, M., Winer, J., Rose, M. & Sewry, C., 1 Nov 2010, In: Journal of Neurology, Neurosurgery and Psychiatry. 81, 11, p. 1182-8 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  50. 2011
  51. 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

  52. 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

  53. 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

  54. 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

  55. 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

  56. 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

  57. 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

  58. 2012
  59. Published

    Blocked muscle fat oxidation during exercise in neutral lipid storage disease

    Laforêt, P., Ørngreen, M., Preisler, N., Andersen, G. & Vissing, John, 2012, In: Archives of Neurology. 69, 4, p. 530-3 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  60. Published

    Calpain 3 is important for muscle regeneration: evidence from patients with limb girdle muscular dystrophies

    Hauerslev, S., Sveen, M., Duno, M., Angelini, C., Vissing, John & Krag, T. O., 2012, In: B M C Musculoskeletal Disorders. 13, p. 43-53 11 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  61. Published

    Cardiac manifestations of myotonic dystrophy type 1

    Petri, H., Vissing, John, Witting, N., Bundgaard, H. & Køber, Lars Valeur, 2012, In: International Journal of Cardiology. 160, 2, p. 82-8 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

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