John Vissing

John Vissing

Clinical Professor

Member of:

  • Neurology


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  1. 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

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

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

  4. Published

    1st International Workshop on Clinical trial readiness for sarcoglycanopathies 15-16 November 2016, Evry, France

    Sarcoglycanopathies Working Group, S. W. G., 2017, In: Neuromuscular Disorders. 27, 7, p. 683-692

    Research output: Contribution to journal › Conference article › Research

  5. Published

    211th ENMC International Workshop: Development of diagnostic criteria and management strategies for McArdle Disease and related rare glycogenolytic disorders to improve standards of care. 17-19 April 2015, Naarden, The Netherlands

    Workshop Participants, W. P. & Vissing, John, 2017, In: Neuromuscular Disorders. 27, 12, p. 1143-1151

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

  6. Published

    216th ENMC international workshop: Clinical readiness in FKRP related myopathies January 15-17, 2016 Naarden, The Netherlands

    Richard, I., Laurent, J., Cirak, S., Vissing, John & ENMC FKRP Study Group, E. F. S. G., Oct 2016, In: Neuromuscular Disorders. 26, 10, p. 717-724 8 p.

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

  7. 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

  8. Published

    229th ENMC international workshop: Limb girdle muscular dystrophies - Nomenclature and reformed classification Naarden, the Netherlands, 17-19 March 2017

    Straub, V., Murphy, A., Udd, B., LGMD workshop study group, L. W. S. G., Angelini, C., Aymé, S., Bönnemann, C., Urtizberea, A., Vissing, John & Walter, M., 2018, In: Neuromuscular Disorders. 28, 8, p. 702-710

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

  9. Published

    233rd ENMC International Workshop: Clinical Trial Readiness for Calpainopathies, Naarden, The Netherlands, 15-17 September 2017

    Lostal, W., Urtizberea, J. A., Richard, I., calpain 3 study group, C. 3. S. G., Alonso-Jiménez, A., Carlier, R., Carson, V., Vainzof, M., Vissing, John & Walter, M., 2018, In: Neuromuscular Disorders. 28, 6, p. 540-549

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

  10. Published

    251st ENMC international workshop: Polyglucosan storage myopathies 13–15 December 2019, Hoofddorp, the Netherlands

    Laforêt, P., Oldfors, A., Malfatti, E., Vissing, J., Colle, M. A., Duran, J., Gentry, M., Guinovart, J., Hurley, T., Kakhlon, O., Krag, T., Landy, H., Lilleør, C. B., Minassian, B., Mingozzi, F., Murphy, E., Piercy, R., Piraud, M., Ramanan, V., Stemmerik, M. & 3 others, Thomsen, C., Weil, M. & ENMC 251st workshop study group, E. 2. W. S. G., 2021, In: Neuromuscular Disorders. 31, 5, p. 466-477 12 p.

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

  11. 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

  12. Published

    263rd ENMC International Workshop: Focus on female carriers of dystrophinopathy: refining recommendations for prevention, diagnosis, surveillance, and treatment. Hoofddorp, The Netherlands, 13-15 May 2022

    Sarkozy, A., Quinlivan, R., Bourke, J. P., Ferlini, A., Barthélémy, I., Cripe, L. H., Reuben, E., Evangelista, T., Florian, A., Gribnau, J., Gonzalez-Quereda, L., Guglieri, M., Niks, E., Phadke, R., Politano, L., Quinlivan, R., Vissing, J., Voermans, N., Vroom, E., Pietrusz, A. & 3 others, Fortunato, F., Houwen, S. & ENMC 263rd Workshop Study Group, E. 2. W. S. G., 2023, In: Neuromuscular Disorders. 33, 3, p. 274-284 11 p.

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

  13. Published

    264th ENMC International Workshop: Multi-system involvement in spinal muscular atrophy Hoofddorp, the Netherlands, November 19th – 21st 2021

    Industry participants, I. P. & Workshop Participants, W. P., 2022, In: Neuromuscular Disorders. 32, 8, p. 697-705 9 p.

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

  14. Published

    265th ENMC International Workshop: Muscle imaging in Facioscapulohumeral Muscular Dystrophy (FSHD): relevance for clinical trials. 22–24 April 2022, Hoofddorp, The Netherlands

    Monforte, M., Attarian, S., Vissing, John, Diaz-Manera, J., Tasca, G. & 265th ENMC workshop participants, 2. E. W. P., 2023, In: Neuromuscular Disorders. 33, 1, p. 65-75 11 p.

    Research output: Contribution to journal › Journal article › Communication

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

  16. Published

    BAG3 myopathy is not always associated with cardiomyopathy

    Andersen, A. G., Fornander, F., Schrøder, H. D., Krag, T., Straub, V., Duno, M. & Vissing, John, 2018, In: Neuromuscular Disorders. 28, 9, p. 798-801

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

  17. Published

    MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement

    Care4Rare Canada Consortium, C. C. C., Dec 2019, In: Acta Neuropathologica. 138, 6, p. 1013-1031 19 p.

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

  18. Published

    NEB mutations disrupt the super-relaxed state of myosin and remodel the muscle metabolic proteome in nemaline myopathy

    Ranu, N., Laitila, J., Dugdale, H. F., Mariano, J., Kolb, J. S., Wallgren-Pettersson, C., Witting, N., Vissing, J., Vilchez, J. J., Fiorillo, C., Zanoteli, E., Auranen, M., Jokela, M., Tasca, G., Claeys, K. G., Voermans, N. C., Palmio, J., Huovinen, S., Moggio, M., Beck, T. N. & 3 others, Kontrogianni-Konstantopoulos, A., Granzier, H. & Ochala, Julien, 2022, In: Acta Neuropathologica Communications. 10, 185.

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

  19. Published

    Nampt controls skeletal muscle development by maintaining Ca2+ homeostasis and mitochondrial integrity

    Basse, A. L., Agerholm, M., Farup, J., Dalbram, E., Nielsen, J., Ørtenblad, N., Altıntaş, A., Ehrlich, A. M., Krag, T., Bruzzone, S., Dall, M., de Guia, R. M., Jensen, J. B., Møller, A. B., Karlsen, A., Kjær, M., Barrès, R., Vissing, J., Larsen, S., Jessen, N. & 1 others, Treebak, Jonas Thue, 2021, In: Molecular Metabolism. 53, 101271.

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

  20. 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

  21. Published

    A New Glycogen Storage Disease Caused by a Dominant PYGM Mutation

    Echaniz-Laguna, A., Lornage, X., Laforêt, P., Orngreen, M. C., Edelweiss, E., Brochier, G., Bui, M. T., Silva-Rojas, R., Birck, C., Lannes, B., Romero, N. B., Vissing, John, Laporte, J. & Böhm, J., 2020, In: Annals of Neurology. 88, 2, p. 274-282

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

  22. Published

    A New Mouse Model of Limb-Girdle Muscular Dystrophy Type 2I Homozygous for the Common L276I Mutation Mimicking the Mild Phenotype in Humans

    Krag, T. O. & Vissing, John, Dec 2015, In: Journal of Neuropathology and Experimental Neurology. 74, 12, p. 1137-46 10 p.

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

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

  24. 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

  25. Published

    A mitochondrial tRNA(Met) mutation causing developmental delay, exercise intolerance and limb girdle phenotype with onset in early childhood

    Born, A. P., Duno, M., Rafiq, J., Risom, L., Wibrand, F., Østergaard, Elsebet & Vissing, John, Jan 2015, In: European Journal of Paediatric Neurology. 19, 1, p. 69-71 3 p.

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

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