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

  62. 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

  63. 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

  64. 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

  65. 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

  66. 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

  67. 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

  68. 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

  69. 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

  70. 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

  71. 2013
  72. 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

  73. 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

  74. 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

  75. 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

  76. 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

  77. 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

  78. 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

  79. 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

  80. 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

  81. 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

  82. 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

  83. 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

  84. 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

  85. 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

  86. 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

  87. 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

  88. Published

    Muscle regeneration and inflammation in patients with facioscapulohumeral muscular dystrophy

    Hauerslev, S., Ørngreen, M. C., Hertz, J. M., Vissing, John & Krag, T. O., 2013, In: Acta Neurologica Scandinavica. 128, 3, p. 194-201 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  89. Published

    Muscle regeneration in mitochondrial myopathies

    Krag, T. O., Hauerslev, S., Dysgaard, Tina, Duno, M. & Vissing, John, 2013, In: Mitochondrion. 13, 2, p. 63-70 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  90. Published

    Myopathic EMG findings and type II muscle fiber atrophy in patients with Lambert-Eaton myasthenic syndrome

    Crone, C., Christiansen, I. & Vissing, John, 2013, In: Clinical Neurophysiology. 124, 9, p. 1889-1892 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  91. Published

    Protein Turnover and Cellular Stress in Mildly and Severely Affected Muscles from Patients with Limb Girdle Muscular Dystrophy Type 2I

    Hauerslev, S., Sveen, M., Vissing, John & Krag, T. O., 2013, In: P L o S One. 8, 6, 7 p., e66929.

    Research output: Contribution to journalJournal articleResearchpeer-review

  92. 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

  93. 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

  94. Published

    Resistance training in patients with limb-girdle and becker muscular dystrophies

    Sveen, M., Andersen, S. P., Ingelsrud, L. H., Blichter, S., Olsen, N. E., Jønck, S., Krag, T. O. & Vissing, John, 2013, In: Muscle & Nerve. 47, 2, p. 163-9 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  95. Published

    Response letter to "Cardiac involvement in myotonic dystrophy type 1 - Do not forget the loop recorder!"

    Petri, H., Vissing, John, Witting, N., Bundgaard, H. & Køber, Lars Valeur, 2013, In: International Journal of Cardiology.

    Research output: Contribution to journalJournal articleResearchpeer-review

  96. Published

    The cytochrome b p.278Y>C mutation causative of a multisystem disorder enhances superoxide production and alters supramolecular interactions of respiratory chain complexes

    Ghelli, A., Tropeano, C. V., Calvaruso, M. A., Marchesini, A., Iommarini, L., Porcelli, A. M., Zanna, C., De Nardo, V., Martinuzzi, A., Wibrand, F., Vissing, John, Kurelac, I., Gasparre, G., Selamoglu, N., Daldal, F. & Rugolo, M., 2013, In: Human Molecular Genetics. 22, 11, p. 2141-2151 11 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  97. Published

    Lactate metabolism during exercise in patients with mitochondrial myopathy

    Dysgaard, Tina, Ørngreen, M. C., van Hall, Gerrit & Vissing, John, 6 Jul 2013, In: Neuromuscular Disorders. 23, 8, p. 629-36 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  98. 2014
  99. Published

    Anti-gravity training improves walking capacity and postural balance in patients with muscular dystrophy

    Berthelsen, M. P., Husu, E., Christensen, S. B., Prahm, K. P., Vissing, John & Jensen, B. R., 2014, In: Neuromuscular Disorders. 24, 6, p. 492-498 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  100. Published

    Decreased Variability of the 6-Minute Walk Test by Heart Rate Correction in Patients with Neuromuscular Disease

    Prahm, K. P., Witting, N. & Vissing, John, 2014, In: PLOS ONE. 9, 12, p. 1-8 8 p., e114273.

    Research output: Contribution to journalJournal articleResearchpeer-review

  101. Published

    Delayed diagnosis of oculopharyngeal muscular dystrophy in Denmark: from initial ptosis to genetic testing

    Mensah, A., Witting, N., Duno, M., Milea, D. & Vissing, John, 2014, In: Acta Ophthamologica (Online). 92, 3, p. e247-e249

    Research output: Contribution to journalComment/debateResearchpeer-review

  102. Published

    Effect of enzyme replacement therapy on isokinetic strength for all major muscle groups in four patients with Pompe disease—a long-term follow-up

    Andreassen, C. S., Schlütter, J. M., Vissing, John & Andersen, H., 2014, In: Molecular Genetics and Metabolism. 112, 1, p. 40-43 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  103. Published

    Insulin Resistance and Increased Muscle Cytokine Levels in Patients With Mitochondrial Myopathy

    Rue, N., Vissing, John & Galbo, Henrik, 2014, In: Journal of Clinical Endocrinology and Metabolism. 99, 10, p. 3757-3765 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  104. Published

    Muscle Atrophy Reversed by Growth Factor Activation of Satellite Cells in a Mouse Muscle Atrophy Model

    Hauerslev, S., Vissing, John & Krag, T. O., 2014, In: PLOS ONE. 9, 6, p. 1-12 12 p., e100594.

    Research output: Contribution to journalJournal articleResearchpeer-review

  105. Published

    Myocardial fibrosis in patients with myotonic dystrophy type 1: a cardiovascular magnetic resonance study

    Petri, H., Ahtarovski, K. A., Vejlstrup, N., Vissing, John, Witting, N., Køber, Lars Valeur & Bundgaard, H., 2014, In: Journal of Cardiovascular Magnetic Resonance. 16, p. 1-10 10 p., 59.

    Research output: Contribution to journalJournal articleResearchpeer-review

  106. Published

    Quantitative magnetic resonance imaging in limb-girdle muscular dystrophy 2I: a multinational cross-sectional study

    Willis, T. A., Hollingsworth, K. G., Coombs, A., Sveen, M., Andersen, S., Stojkovic, T., Eagle, M., Mayhew, A., de Sousa, P. L., Dewar, L., Morrow, J. M., Sinclair, C. D. J., Thornton, J. S., Bushby, K., Lochmuller, H., Hanna, M. G., Hogrel, J., Carlier, P. G., Vissing, John & Straub, V., 2014, In: PloS one. 9, 2, p. 1-9 9 p., e90377.

    Research output: Contribution to journalJournal articleResearchpeer-review

  107. Published

    Severe Axial Myopathy in McArdle Disease

    Witting, N., Duno, M., Piraud, M. & Vissing, John, Jan 2014, In: J A M A Neurology. 71, 1, p. 88-90 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  108. Published

    A novel de novo mutation of the mitochondrial tRNAlys gene mt.8340G>a associated with pure myopathy

    Jeppesen, T. D., Duno, M., Risom, L., Wibrand, F., Rafiq, J., Krag, T., Jakobsen, J., Andersen, H. & Vissing, John, Feb 2014, In: Neuromuscular Disorders. 24, 2, p. 162-166 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  109. Published

    A pilot study of muscle plasma protein changes after exercise

    Dahlqvist, J. R., Voss, L. G., Lauridsen, T., Krag, T. O. & Vissing, John, Feb 2014, In: Muscle & Nerve. 49, 2, p. 261-266 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  110. Published

    Bezafibrate in skeletal muscle fatty acid oxidation disorders: A randomized clinical trial

    Ørngreen, M. C., Madsen, K. L., Preisler, N., Andersen, G., Vissing, John & Laforêt, P., 18 Feb 2014, In: Neurology. 82, 7, p. 607-613 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  111. Published

    Reduced ceramide synthase 2 activity causes progressive myoclonic epilepsy

    Mosbech, M., Olsen, A. S. B., Neess, D., Ben-David, O., Klitten, L. L., Larsen, J., Sabers, A., Vissing, John, Nielsen, Jørgen Erik, Hasholt, Lis Frydenreich, Klein, A. D., Tsoory, M. M., Hjalgrim, H., Tommerup, Niels, Futerman, A. H., Møller, R. S. & Færgeman, N. J., 28 Feb 2014, In: Annals of Clinical and Translational Neurology. 1, 2, p. 88-98 11 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  112. Published

    Pharmacologic Treatment of Downstream of Tyrosine Kinase 7 Congenital Myasthenic Syndrome

    Witting, N. & Vissing, John, Mar 2014, In: Archives of Neurology. 71, 3, p. 350-354 5 p.

    Research output: Contribution to journalReviewResearchpeer-review

  113. Published

    Frequency and phenotype of patients carrying TPM2 and TPM3 gene mutations in a cohort of 94 patients with congenital myopathy

    Citirak, G., Witting, N., Duno, M., Werlauff, U., Petri, H. & Vissing, John, Apr 2014, In: Neuromuscular Disorders. 24, 4, p. 325-30 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

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