John Vissing

John Vissing

Clinical Professor

Member of:

  • Neurology


  1. 2023
  2. Published

    Efficacy and Safety of Elamipretide in Individuals with Primary Mitochondrial Myopathy: The MMPOWER-3 Randomized Clinical Trial

    Karaa, A., Bertini, E., Carelli, V., Cohen, B. H., Enns, G. M., Falk, M. J., Goldstein, A., Gorman, G. S., Haas, R., Hirano, M., Klopstock, T., Koenig, M. K., Kornblum, C., Lamperti, C., Lehman, A., Longo, N., Molnar, M. J., Parikh, S., Phan, H., Pitceathly, R. D. S. & 12 others, Saneto, R., Scaglia, F., Servidei, S., Tarnopolsky, M., Toscano, A., Van Hove, J. L. K., Vissing, John, Vockley, J., Finman, J. S., Brown, D. A., Shiffer, J. A. & Mancuso, M., 2023, In: Neurology. 101, 3, p. e238-e252

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. 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 journalJournal articleResearchpeer-review

  4. Published

    Can a modified ketogenic diet be a nutritional strategy for patients with McArdle disease? Results from a randomized, single-blind, placebo-controlled, cross-over study

    Løkken, N., Nielsen, M. R., Stemmerik, M. G., Ellerton, C., Revsbech, K. L., Macrae, M., Slipsager, A., Krett, B., Beha, G. H., Emanuelsson, F., van Hall, Gerrit, Quinlivan, R. & Vissing, John, 2023, In: Clinical Nutrition. 42, 11, p. 2124-2137 14 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    Patient-Reported Experiences with a Low-Carbohydrate Ketogenic Diet: An International Survey in Patients with McArdle Disease

    Løkken, N., Voermans, N. C., Andersen, L. K., Karazi, W., Reason, S. L., Zweers, H., Wilms, G., Santalla, A., Susanibar, E., Lucia, A. & Vissing, John, 2023, In: Nutrients. 15, 4, 14 p., 843.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    Repeated oral sucrose dosing after the second wind is unnecessary in patients with McArdle disease: Results from a randomized, placebo-controlled, double-blind, cross-over study

    Løkken, N., Khawajazada, T., Slipsager, A., Voermans, N. C. & Vissing, John, 2023, In: Journal of Inherited Metabolic Disease. 46, 6, p. 1139-1146 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. 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 journalJournal articleCommunication

  8. Published

    Low skeletal muscle mass and liver fibrosis in children with cerebral palsy

    Naume, Marie Mostue, Jørgensen, M. H., Høi-Hansen, Christina Engel, Nielsen, M. R., Born, A. P., Vissing, John, Borgwardt, L., Stærk, D. M. R. & Ørngreen, M. C., 2023, In: European Journal of Pediatrics. 182, 11, p. 5047-5055 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    Metabolic assessment in children with neuromuscular disorders shows risk of liver enlargement, steatosis and fibrosis

    Naume, Marie Mostue, Jørgensen, M. H., Høi-Hansen, Christina Engel, Born, A. P., Vissing, John, Borgwardt, L., Stærk, D. M. R. & Ørngreen, M. C., 2023, In: Acta Paediatrica, International Journal of Paediatrics. 112, 4, p. 846-853

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. 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 journalConference articleResearchpeer-review

  11. Published

    Abnormal myosin post-translational modifications and ATP turnover time associated with human congenital myopathy-related RYR1 mutations

    Sonne, A., Antonovic, A. K., Thomsen, Elise Julie Melhedegaard, Akter, F., Andersen, J. L., Jungbluth, H., Witting, N., Vissing, John, Zanoteli, E., Fornili, A. & Ochala, Julien, 2023, In: Acta Physiologica. 239, 2, 14 p., e14035.

    Research output: Contribution to journalJournal articleResearchpeer-review

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ID: 915367