John Vissing

John Vissing

Clinical Professor

Member of:

  • Neurology


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  1. Published

    Limb girdle muscular dystrophies: classification, clinical spectrum and emerging therapies

    Vissing, John, Oct 2016, In: Current Opinion in Neurology. 29, 5, p. 635-641 7 p.

    Research output: Contribution to journal › Review › Research › peer-review

  2. 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 journal › Journal article › Research › peer-review

  3. Published

    Paternal comeback in mitochondrial DNA inheritance

    Vissing, John, 2019, In: Proceedings of the National Academy of Sciences of the United States of America. 116, 5, p. 1475-1476

    Research output: Contribution to journal › Comment/debate › Research

  4. Published

    Editorial: Remaining diagnostic issues and start of a treatment era for muscle diseases

    Vissing, John, 2020, In: Current Opinion in Neurology. 33, 5, p. 587-589 3 p.

    Research output: Contribution to journal › Editorial › Research › peer-review

  5. 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 journal › Journal article › Research › peer-review

  6. Published

    A heterozygous 21-bp deletion in CAPN3 causes dominantly inherited limb girdle muscular dystrophy

    Vissing, John, Barresi, R., Witting, N., Van Ghelue, M., Gammelgaard, L., Bindoff, L. A., Straub, V., Lochmüller, H., Hudson, J., Arnardottir, S., Dahlbom, K., Jonsrud, C. & Duno, M., 30 Apr 2016, In: Brain. 139, 8, p. 2154-2163 10 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  7. 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 proceeding › Book chapter › Education

  8. Published

    A single c.1715G>C calpain 3 gene variant causes dominant calpainopathy with loss of calpain 3 expression and activity

    Vissing, John, Dahlqvist, J. R., Roudaut, C., Poupiot, J., Richard, I., Duno, M. & Krag, T., 2020, In: Human Mutation. 41, 9, p. 1507-1513

    Research output: Contribution to journal › Journal article › Research › peer-review

  9. Published

    Correlation between myasthenia gravis-activities of daily living (MG-ADL) and quantitative myasthenia gravis (QMG) assessments of anti-acetylcholine receptor antibody-positive refractory generalized myasthenia gravis in the phase 3 regain study

    Vissing, John, O'Brien, F., Wang, J. J. & Howard, J. F., 2018, In: Muscle & Nerve. 58, 2, p. E21-E22

    Research output: Contribution to journal › Journal article › Research › peer-review

  10. 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 journal › Journal article › Research › peer-review

  11. Published

    POPDC3 Gene Variants Associate with a New Form of Limb Girdle Muscular Dystrophy

    Vissing, John, Johnson, K., Töpf, A., Nafissi, S., Díaz-Manera, J., French, V. M., Schindler, R. F., Sarathchandra, P., Løkken, N., Rinné, S., Freund, M., Decher, N., Müller, T., Duno, M., Krag, T., Brand, T. & Straub, V., Dec 2019, In: Annals of Neurology. 86, 6, p. 832-843 12 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  12. 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 journal › Journal article › Research › peer-review

  13. 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 journal › Journal article › Research › peer-review

  14. 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 journal › Journal article › Research › peer-review

  15. Published

    Reply: Dominant LGMD2A: Alternative diagnosis or hidden digenism?

    Vissing, John & Duno, M., 2017, In: Brain. 140, 2, 2 p., e8.

    Research output: Contribution to journal › Comment/debate › Research

  16. Published

    ‘Minimal symptom expression’ in patients with acetylcholine receptor antibody-positive refractory generalized myasthenia gravis treated with eculizumab

    Vissing, J., Jacob, S., Fujita, K. P., O’Brien, F., Howard, J. F., The REGAIN Study Group, Mazia, C. G., Wilken, M., Barroso, F., Saba, J., Rugiero, M., Bettini, M., Chaves, M., Vidal, G., Garcia, A. D., De Bleecker, J., Van den Abeele, G., de Koning, K., De Mey, K., Mercelis, R. & 36 others, Mahieu, D., Wagemaekers, L., Van Damme, P., Depreitere, A., Schotte, C., Smetcoren, C., Stevens, O., Van Daele, S., Vandenbussche, N., Vanhee, A., Verjans, S., Vynckier, J., D’Hont, A., Tilkin, P., Alves de Siqueira Carvalho, A., Dias Brockhausen, I., Feder, D., Ambrosio, D., César, P., Melo, A. P., Martins Ribeiro, R., Rocha, R., Rosa, B. B., Veiga, T., da Silva, L. A., Andersen, H., Harbo, T., Vinge, L., Krogh, S., Mogensen, A., Vissing, John, Højgaard, J., Witting, N., Autzen, A. M. O., Pedersen, J. & Weiss, M., 2020, In: Journal of Neurology. 267, p. 1991-2001

    Research output: Contribution to journal › Journal article › Research › peer-review

  17. 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 proceeding › Book chapter › Education

  18. Published

    Level of residual enzyme activity modulates the phenotype in phosphoglycerate kinase deficiency

    Vissing, John, Akman, H. O., Aasly, J., Kahler, S. G., Bacino, C. A., DiMauro, S. & Haller, R. G., 2018, In: Neurology. 91, 11, p. e1077-e1082

    Research output: Contribution to journal › Journal article › Research › peer-review

  19. Published

    Remodel mitochondria and get energized

    Vissing, John & Angelini, C., 2018, In: Neurology. 90, 14, p. 633-634

    Research output: Contribution to journal › Editorial › Research

  20. Published

    PGM1 deficiency: Substrate use during exercise and effect of treatment with galactose

    Voermans, N. C., Preisler, N., Madsen, K. L., Janssen, M. C. H., Kusters, B., Abu Bakar, N., Conte, F., Lamberti, V. M. L., Nusman, F., van Engelen, B. G., van Scherpenzeel, M., Vissing, John & Lefeber, D. J., 2017, In: Neuromuscular Disorders. 27, 4, p. 370-376

    Research output: Contribution to journal › Journal article › Research › peer-review

  21. 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 proceeding › Book chapter › Research

  22. Published

    Improving Care and Empowering Adults Living with SMA: A Call to Action in the New Treatment Era

    Walter, M. C., Chiriboga, C., Duong, T., Goemans, N., Mayhew, A., Ouillade, L., Oskoui, M., Quinlivan, R., Vázquez-Costa, J. F., Vissing, John & Servais, L., 2021, In: Journal of Neuromuscular Diseases. 8, 4, p. 543-551 9 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  23. Published

    254th ENMC international workshop. Formation of a European network to initiate a European data collection, along with development and sharing of treatment guidelines for adult SMA patients. Virtual meeting 28 – 30 January 2022

    254th ENMC Workshop Study Group, 2. E. W. S. G., 2023, In: Neuromuscular Disorders. 33, 6, p. 511-522 12 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  24. 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 journal › Journal article › Research › peer-review

  25. Published

    Progression or Not - A Small Natural History Study of Genetical Confirmed Congenital Myopathies

    Werlauff, U., Hansen, P. D., Witting, N. & Vissing, John, 2021, In: Journal of Neuromuscular Diseases. 8, 4, p. 647-655 9 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  26. Published

    Fatigue in patients with spinal muscular atrophy type II and congenital myopathies: evaluation of the fatigue severity scale

    Werlauff, U., Højberg, A., Firla-Holme, R., Steffensen, B. F. & Vissing, John, Jun 2014, In: Quality of Life Research. 23, 5, p. 1479-1488 10 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  27. 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 journal › Journal article › Research › peer-review

  28. 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 journal › Journal article › Research › peer-review

  29. 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 journal › Journal article › Research › peer-review

  30. Published

    Phenotype and genotype of muscle ryanodine receptor rhabdomyolysis-myalgia syndrome

    Witting, N., Laforêt, P., Voermans, N. C., Roux-Buisson, N., Bompaire, F., Rendu, J., Duno, M., Feillet, F., Kamsteeg, E., Poulsen, N. S., Dahlqvist, J. R., Romero, N. B., Fauré, J., Vissing, John & Behin, A., 2018, In: Acta Neurologica Scandinavica. 137, 5, p. 452-461 10 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  31. Published

    A third case of congenital myasthenic syndrome caused by mutations in SCN4A

    Witting, N., Werlauff, U., Ballegaard, Martin & Vissing, John, Oct 2015, p. S209-S209. 1 p.

    Research output: Contribution to conference › Poster › Research › peer-review

  32. Published

    Botulinum toxin treatment improves dysphagia in patients with oculopharyngeal muscular dystrophy and sporadic inclusion body myositis

    Witting, N., Daugaard, D., Prytz, S., Biernat, H., Diederichsen, Louise C P Raun & Vissing, John, 2022, In: Journal of Neurology. 269, 8, p. 4154-4160 7 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  33. 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 journal › Journal article › Research › peer-review

  34. Published

    Axial myopathy: an overlooked feature of muscle diseases

    Witting, N., Andersen, L. K. & Vissing, John, 2016, In: Brain. 139, 1, p. 13-22 10 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  35. Published

    Effect of sildenafil on skeletal and cardiac muscle in Becker muscular dystrophy

    Witting, N., Kruuse, Christina Rostrup, Nyhuus, B., Prahm, K. P., Citirak, G., Lundgaard, S. J., von Huth, S., Vejlstrup, N., Lindberg, U., Krag, T. O. & Vissing, John, Oct 2014, In: Annals of Neurology. 76, 4, p. 550–557 8 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  36. Published

    Clinical and neurophysiological response to pharmacological treatment of DOK7 congenital myasthenia in an older patient

    Witting, N., Crone, C., Duno, M. & Vissing, John, Mar 2015, In: Clinical Neurology and Neurosurgery. 130, p. 168-70 3 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  37. 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 journal › Journal article › Research › peer-review

  38. 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 journal › Review › Research › peer-review

  39. 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 journal › Journal article › Research › peer-review

  40. Published

    Collagen XII myopathy with rectus femoris atrophy and collagen XII retention in fibroblasts

    Witting, N., Krag, T., Werlauff, U., Duno, M., Oestergaard, S. T., Dahlqvist, J. R. & Vissing, John, 2018, In: Muscle & Nerve. 57, 6, p. 1026-1030

    Research output: Contribution to journal › Journal article › Research › peer-review

  41. 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 journal › Journal article › Research › peer-review

  42. Published

    Phenotypes, genotypes, and prevalence of congenital myopathies older than 5 years in Denmark

    Witting, N., Werlauff, U., Duno, M. & Vissing, John, Apr 2017, In: Neurology: Genetics. 3, 2, 15 p., e140.

    Research output: Contribution to journal › Journal article › Research › peer-review

  43. Published

    Prevalence and phenotypes of congenital myopathy due to α-actin 1 gene mutations

    Witting, N., Werlauff, U., Duno, M. & Vissing, John, Mar 2016, In: Muscle & Nerve. 53, 3, p. 388-93 6 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  44. 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 journal › Journal article › Research › peer-review

  45. Published

    222nd ENMC International Workshop: Myotonic dystrophy, developing a European consortium for care and therapy, Naarden, The Netherlands, 1-2 July 2016

    Wood, L., Bassez, G., van Engelen, B., Lochmüller, H., Schoser, B., 222nd ENMC workshop participants, 2. E. W. P., Atalaiae, A., Balabanovf, P., Bassez, G., Treweek, S., Vissing, John & Wood, L., 2018, In: Neuromuscular Disorders. 28, 5, p. 463-469

    Research output: Contribution to journal › Comment/debate › Research

  46. Published

    Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy

    Zaharieva, I. T., Thor, M. G., Oates, E. C., van Karnebeek, C., Hendson, G., Blom, E., Witting, N., Rasmussen, M., Gabbett, M. T., Ravenscroft, G., Sframeli, M., Suetterlin, K., Sarkozy, A., D'Argenzio, L., Hartley, L., Matthews, E., Pitt, M., Vissing, J., Ballegaard, M., Krarup, C. & 20 others, Slørdahl, A., Halvorsen, H., Ye, X. C., Zhang, L., Løkken, N., Werlauff, U., Abdelsayed, M., Davis, M. R., Feng, L., Phadke, R., Sewry, C. A., Morgan, J. E., Laing, N. G., Vallance, H., Ruben, P., Hanna, M. G., Lewis, S., Kamsteeg, E., Männikkö, R. & Muntoni, F., 2016, In: Brain. 139, 3, p. 674-91 18 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  47. Published

    European consensus for starting and stopping enzyme replacement therapy in adult patients with Pompe disease: a 10-year experience

    van der Ploeg, A. T., Kruijshaar, M. E., Toscano, A., Laforêt, P., Angelini, C., Lachmann, R. H., Pascual Pascual, S. I., Roberts, M., Rösler, K., Stulnig, T. M., van Doorn, P. A., Van den Bergh, P. Y. K., Vissing, John, Schoser, B. & European Pompe Consortium, E. P. C., Jun 2017, In: European Journal of Neurology. 24, 6, p. 768-e31

    Research output: Contribution to journal › Journal article › Research › peer-review

  48. 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 journal › Journal article › Research › peer-review

  49. 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 journal › Journal article › Research › peer-review

  50. 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 journal › Journal article › Research › peer-review

  51. 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 journal › Journal article › Research › peer-review

  52. Published

    Treatment Opportunities in Patients With Metabolic Myopathies

    Ørngreen, M. C. & Vissing, John, 2017, In: Current Treatment Options in Neurology. 19, 11, 16 p., 37.

    Research output: Contribution to journal › Review › Research › peer-review

  53. Published

    Lactate and Energy Metabolism During Exercise in Patients With Blocked Glycogenolysis (McArdle Disease)

    Ørngreen, M. C., Jeppesen, T. D., Taivassalo, T., Hauerslev, S., Preisler, N., Heinicke, K., Haller, R. G., Vissing, John & van Hall, Gerrit, Aug 2015, In: Journal of Clinical Endocrinology and Metabolism. 100, 8, p. E1096-E1104 9 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  54. Published

    No effect of bezafibrate in patients with CPTII and VLCAD deficiencies

    Ørngreen, M. C., Vissing, John & Laforét, P., Mar 2015, In: Journal of Inherited Metabolic Disease. 38, 2, p. 373-4 2 p.

    Research output: Contribution to journal › Comment/debate › Research › peer-review

  55. Published

    Limb girdle muscular dystrophy due to mutations in POMT2

    Østergaard, S. T., Johnson, K., Stojkovic, T., Krag, T., De Ridder, W., De Jonghe, P., Baets, J., Claeys, K. G., Fernández-Torrón, R., Phillips, L., Topf, A., Colomer, J., Nafissi, S., Jamal-Omidi, S., Bouchet-Seraphin, C., Leturcq, F., MacArthur, D. G., Lek, M., Xu, L., Nelson, I. & 2 others, Straub, V. & Vissing, John, 2018, In: Journal of neurology, neurosurgery, and psychiatry. 89, 5, p. 506-512

    Research output: Contribution to journal › Journal article › Research › peer-review

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