John Vissing

John Vissing

Clinical Professor

Member of:

  • Neurology


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

  2. 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

  3. Published

    Combined Muscle Biopsy and Comprehensive Electrophysiology in General Anesthesia is Valuable in Diagnosis of Neuromuscular Disease in Children

    Høi-Hansen, Christina Engel, Tygesen, M. L. B., Dunø, M., Vissing, John, Ballegaard, Martin & Born, P., 2021, In: Neuropediatrics. 52, 6, p. 462-468

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

  4. Published

    Congenital Titinopathy: Comprehensive characterization and pathogenic insights

    Oates, E. C., Jones, K. J., Donkervoort, S., Charlton, A., Brammah, S., Smith, J. E., Ware, J. S., Yau, K. S., Swanson, L. C., Whiffin, N., Peduto, A. J., Bournazos, A., Waddell, L. B., Farrar, M. A., Sampaio, H. A., Teoh, H. L., Lamont, P. J., Mowat, D., Fitzsimons, R. B., Corbett, A. J. & 64 others, Ryan, M. M., O'Grady, G. L., Sandaradura, S. A., Ghaoui, R., Joshi, H., Marshall, J. L., Nolan, M. A., Kaur, S., Punetha, J., Töpf, A., Harris, E., Bakshi, M., Genetti, C. A., Marttila, M., Werlauff, U., Streichenberger, N., Pestronk, A., Mazanti, I., Pinner, J. R., Vuillerot, C., Grosmann, C., Camacho, A., Mohassel, P., Leach, M. E., Foley, A. R., Bharucha-Goebel, D., Collins, J., Connolly, A. M., Gilbreath, H. R., Iannaccone, S. T., Castro, D., Cummings, B. B., Webster, R. I., Lazaro, L., Vissing, John, Coppens, S., Deconinck, N., Luk, H. M., Thomas, N. H., Foulds, N. C., Illingworth, M. A., Ellard, S., McLean, C. A., Phadke, R., Ravenscroft, G., Witting, N., Hackman, P., Richard, I., Cooper, S. T., Kamsteeg, E. J., Hoffman, E. P., Bushby, K., Straub, V., Udd, B., Ferreiro, A., North, K. N., Clarke, N. F., Lek, M., Beggs, A. H., Bönnemann, C. G., MacArthur, D. G., Granzier, H., Davis, M. R. & Laing, N. G., 2018, In: Annals of Neurology. 83, 6, p. 1105-1124 20 p.

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

  5. Published

    Congenital myopathies are mainly associated with a mild cardiac phenotype

    Petri, H., Wahbi, K., Witting, N., Køber, Lars Valeur, Bundgård, Henning, Kamoun, E., Vellieux, G., Stojkovic, T., Béhin, A., Laforet, P. & Vissing, John, Jun 2019, In: Journal of Neurology. 266, 6, p. 1367-1375 9 p.

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

  6. Published

    Contractile properties are disrupted in Becker muscular dystrophy, but not in limb girdle type 2I

    Løkken, N., Hedermann, G., Thomsen, C. & Vissing, John, Sep 2016, In: Annals of Neurology. 80, 3, p. 466-471 6 p.

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

  7. Published

    Contractile properties are impaired in congenital myopathies

    Eisum, A. V., Fornander, F., Poulsen, N. S., Andersen, A. G., Dahlqvist, J., Andersen, L. K., Witting, N. & Vissing, John, 1 Aug 2020, In: Neuromuscular Disorders. 30, 8, p. 649-655 7 p.

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

  8. 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

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

  10. Published

    Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry)

    Pinós, T., Andreu, A. L., Bruno, C., Hadjigeorgiou, G. M., Haller, R., Laforêt, P., Lucía, A., Martín, M. A., Martinuzzi, A., Navarro, C., Oflazer, P., Pouget, J., Quinlivan, R., Sacconi, S., Scalco, R. S., Toscano, A., Vissing, J., Vorgerd, M., Wakelin, A., Martí, R. & 14 others, Baruch, N., Ortega, F. J., San-Millán, B., Vieitez, I., Vavla, M., Musumeci, O., Scalco, R., Hadjgeorgiou, G., Zintzaras, E., Zülow, E., Haller, R., Durmus, H., Santalla, A. & EUROMAC Consortium, E. C., 2020, In: Orphanet Journal of Rare Diseases. 15, 1, 187.

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

  11. Published

    Cytokine genes as potential biomarkers for muscle weakness in OPMD

    Riaz, M., Raz, Y., van der Slujis, B., Dickson, G., van Engelen, B., Vissing, John & Raz, V., 1 Oct 2016, In: Human Molecular Genetics. 25, 19, p. 4282-4287 6 p.

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

  12. Published

    DOK7 congenital myasthenia may be associated with severe mitral valve insufficiency

    Gaist, D., Mogensen, J., Pedersen, E. G., Schrøder, H. D., Vissing, John, Andersen, H. & Hertz, J. M., 15 Aug 2017, In: Journal of the Neurological Sciences. 379, p. 217-218 2 p.

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

  13. Published

    Data from the European registry for patients with McArdle disease (EUROMAC): functional status and social participation

    Karazi, W., Scalco, R. S., Stemmerik, M. G., Løkken, N., Lucia, A., Santalla, A., Martinuzzi, A., Vavla, M., Reni, G., Toscano, A., Musumeci, O., Kouwenberg, C. V., Laforêt, P., Millán, B. S., Vieitez, I., Siciliano, G., Kühnle, E., Trost, R., Sacconi, S., Durmus, H. & 9 others, Kierdaszuk, B., Wakelin, A., Andreu, A. L., Pinós, T., Marti, R., Quinlivan, R., Vissing, John, Voermans, N. C. & EUROMAC Consortium, E. C., 2023, In: Orphanet Journal of Rare Diseases. 18, 9 p., 210.

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

  14. Published

    Data from the European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC)

    Scalco, R. S., Lucia, A., Santalla, A., Martinuzzi, A., Vavla, M., Reni, G., Toscano, A., Musumeci, O., Voermans, N. C., Kouwenberg, C. V., Laforêt, P., San-Millán, B., Vieitez, I., Siciliano, G., Kühnle, E., Trost, R., Sacconi, S., Stemmerik, M. G., Durmus, H., Kierdaszuk, B. & 7 others, Wakelin, A., Andreu, A. L., Pinós, T., Marti, R., Quinlivan, R., Vissing, John & EUROMAC Consortium, E. C., 2020, In: Orphanet Journal of Rare Diseases. 15, 1, p. 330

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

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

  16. Published

    Deep morphological analysis of muscle biopsies from type III glycogenesis (GSDIII), debranching enzyme deficiency, revealed stereotyped vacuolar myopathy and autophagy impairment

    Laforêt, P., Inoue, M., Goillot, E., Lefeuvre, C., Cagin, U., Streichenberger, N., Leonard-Louis, S., Brochier, G., Madelaine, A., Labasse, C., Hedberg-Oldfors, C., Krag, T., Jauze, L., Fabregue, J., Labrune, P., Milisenda, J., Nadaj-Pakleza, A., Sacconi, S., Mingozzi, F., Ronzitti, G. & 7 others, Petit, F., Schoser, B., Oldfors, A., Vissing, John, Romero, N. B., Nishino, I. & Malfatti, E., 2019, In: Acta Neuropathologica Communications. 7, 16 p., 167.

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

  17. Published

    Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging

    Giacomucci, G., Monforte, M., Diaz-Manera, J., Mul, K., Fernandez Torrón, R., Maggi, L., Marini Bettolo, C., Dahlqvist, J. R., Haberlova, J., Camaño, P., Gros, M., Tartaglione, T., Cristiano, L., Gerevini, S., Calandra, P., Deidda, G., Giardina, E., Sacconi, S., Straub, V., Vissing, J. & 3 others, Van Engelen, B., Ricci, E. & Tasca, G., 2020, In: European Journal of Neurology. 27, 12, p. 2604-2615 12 p.

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

  18. 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

  19. 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 journal › Comment/debate › Research › peer-review

  20. 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

  21. Published

    Depletion of ATP Limits Membrane Excitability of Skeletal Muscle by Increasing Both ClC1-Open Probability and Membrane Conductance

    Leermakers, P. A., Dybdahl, K. L. T., Husted, K. S., Riisager, A., de Paoli, F. V., Pinós, T., Vissing, John, Krag, T. O. B. & Pedersen, T. H., 2020, In: Frontiers in Neurology. 11, 541.

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

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

  23. Published

    Design of Reach: Phase 3 randomized, double-blind, placebo-controlled, 48-week study of the efficacy and safety of losmapimod in FSHD

    Tawil, R., Han, J., Wang, L., Vissing, John, van Engelen, B., Statland, J., Mellion, M., Shoskes, J., Morabito, C., Jiang, J. & Webster, J., 2022, In: Neuromuscular Disorders. 32, Supplement 1, p. S104-S104 1 p., P.136 .

    Research output: Contribution to journal › Conference abstract in journal › Research › peer-review

  24. Published

    Det komplekse kliniske billede ved arvelige mitokondriesygdomme

    Frederiksen, A. L., Nielsen, M. F., Yderstræde, K. & Vissing, John, 15 Sep 2014, In: Ugeskrift for Laeger. 176, 38, p. 1779-1783 5 p.

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

  25. Published

    Detection of variants in dystroglycanopathy-associated genes through the application of targeted whole-exome sequencing analysis to a large cohort of patients with unexplained limb-girdle muscle weakness

    Johnson, K., Bertoli, M., Phillips, L., Töpf, A., Van den Bergh, P., Vissing, J., Witting, N., Nafissi, S., Jamal-Omidi, S., Łusakowska, A., Kostera-Pruszczyk, A., Potulska-Chromik, A., Deconinck, N., Wallgren-Pettersson, C., Strang-Karlsson, S., Colomer, J., Claeys, K. G., De Ridder, W., Baets, J., von der Hagen, M. & 12 others, Fernández-Torrón, R., Zulaica Ijurco, M., Espinal Valencia, J. B., Hahn, A., Durmus, H., Willis, T., Xu, L., Valkanas, E., Mullen, T. E., Lek, M., MacArthur, D. G. & Straub, V., 2018, In: Skeletal Muscle. 8, 12 p., 23.

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

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ID: 915367