John Vissing

John Vissing

Clinical Professor

Member of:

  • Neurology


  1. 2022
  2. Published

    Home-based gait analysis as an exploratory endpoint during a multicenter phase 1 trial in limb girdle muscular dystrophy type R2 and facioscapulohumeral muscular dystrophy

    Gidaro, T., Gasnier, E., Annoussamy, M., Vissing, John, Attarian, S., Mozaffar, T., Iyadurai, S., Wagner, K. R., Vissiere, D., Walker, G., Shukla, S. S. & Servais, L., 2022, In: Muscle & Nerve. 65, 2, p. 237-242 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    Muscle MRI in McArdle Disease: A European Multicenter Observational Study

    Løkken, N., Revsbech, K. L., Jacobsen, L. N., Martinuzzi, A., Martin, M. Á., Díaz-Manera, J., Dominguez-Gonzalez, C., Brondani, G., Musumeci, O., Granata, F., Stefan, C., Merino-Sanchez, C., Peralta, C. N., Khawajazada, T., Alonso-Pérez, J., Toscano, A. & Vissing, John, 2022, In: Neurology. 99, 15, p. E1664-E1675

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    No effect of oral ketone ester supplementation on exercise capacity in patients with McArdle disease and healthy controls: A randomized placebo-controlled cross-over study

    Løkken, N., Storgaard, J. H., Revsbech, K. L., Voermans, N. C., van Hall, Gerrit, Vissing, John & Ørngreen, M. C., 2022, In: Journal of Inherited Metabolic Disease. 45, 3, p. 502-516 15 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    Global FKRP registry - the research database for limb girdle muscular dystrophy R9 (2I)

    Murphy, L., Alfano, L., Brazzo, K., Johnson, N., Laurent, J., Mathews, K., Thiele, S., Vissing, John, Walter, M., Woods, L., Orstavik, K. & Straub, V., Oct 2022, In: Neuromuscular Disorders. 32, Supplement 1, p. S118-S118 1 p., P.175.

    Research output: Contribution to journalConference abstract in journalResearchpeer-review

  6. Published

    Growth Factors Do Not Improve Muscle Function in Young or Adult mdx Mice

    Nielsen, T. L., Hornsyld, T. M., Pinós, T., Brolin, C., Vissing, John & Krag, T. O., 2022, In: Biomedicines. 10, 2, 304.

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    β-Galactosidase deficiency in the GLB1 spectrum of lysosomal storage disease can present with severe muscle weakness and atrophy

    Pedersen, J. J., Duno, M., Wibrand, F., Hammer, C., Krag, T. & Vissing, John, 2022, In: JIMD Reports. 63, 6, p. 540-545 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    Diagnostic interest of whole-body MRI in early- and late-onset LAMA2 muscular dystrophies: a large international cohort

    Quijano-Roy, S., Haberlova, J., Castiglioni, C., Vissing, J., Munell, F., Rivier, F., Stojkovic, T., Malfatti, E., Gómez García de la Banda, M., Tasca, G., Costa Comellas, L., Benezit, A., Amthor, H., Dabaj, I., Gontijo Camelo, C., Laforêt, P., Rendu, J., Romero, N. B., Cavassa, E., Fattori, F. & 10 others, Beroud, C., Zídková, J., Leboucq, N., Løkken, N., Sanchez-Montañez, Á., Ortega, X., Kynčl, M., Metay, C., Gómez-Andrés, D. & Carlier, R. Y., 2022, In: Journal of Neurology. 269, p. 2414–2429

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    No effect of triheptanoin in patients with phosphofructokinase deficiency

    Raaschou-Pedersen, D. E., Madsen, K. L., Lokken, N., Storgaard, J. H., Quinlivan, R., Laforet, P., Lund, Allan Meldgaard, van Hall, Gerrit, Vissing, John & Orngreen, M., Apr 2022, In: Neuromuscular Disorders. 32, 4, p. 295-304 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. 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 journalJournal articleResearchpeer-review

  11. Published

    High Resolution Analysis of DMPK Hypermethylation and Repeat Interruptions in Myotonic Dystrophy Type 1

    Rasmussen, A., Hildonen, M., Vissing, John, Duno, M., Tümer, Asuman Zeynep & Birkedal, U., 2022, In: Genes. 13, 6, 12 p., 970.

    Research output: Contribution to journalJournal articleResearchpeer-review

Previous 1 2 3 4 5 6 7 8 ...36 Next

ID: 915367