John Vissing

John Vissing

Clinical Professor

Member of:

  • Neurology


Publication year:
All
1 - 30 out of 30Page size: 100
  1. 2017
  2. Published

    Muscle glycogen synthesis and breakdown are both impaired in glycogenin-1 deficiency

    Stemmerik, M. G., Madsen, K. L., Laforêt, P., Buch, A. E. & Vissing, John, 12 Dec 2017, In: Neurology. 89, 24, p. 2491-2494 4 p.

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

  3. Published

    Clinical heterogeneity and phenotype/genotype findings in 5 families with GYG1  deficiency

    Ben Yaou, R., Hubert, A., Nelson, I., Dahlqvist, J. R., Gaist, D., Streichenberger, N., Beuvin, M., Krahn, M., Petiot, P., Parisot, F., Michel, F., Malfatti, E., Romero, N., Carlier, R. Y., Eymard, B., Labrune, P., Duno, M., Krag, T., Cerino, M., Bartoli, M. & 4 others, Bonne, G., Vissing, John, Laforet, P. & Petit, F. M., Dec 2017, In: Neurology: Genetics. 3, 6, 11 p., e208.

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

  4. Published

    Mitochondrial DNA mutation load in a family with the m.8344A>G point mutation and lipomas: a case study

    Jeppesen, T. D., Al-Hashimi, N., Duno, M., Wibrand, F., Andersen, G. & Vissing, John, Dec 2017, In: Clinical Case Reports. 5, 12, p. 2034-2039 6 p.

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

  5. Published

    Safety and efficacy of eculizumab in anti-acetylcholine receptor antibody-positive refractory generalised myasthenia gravis (REGAIN): a phase 3, randomised, double-blind, placebo-controlled, multicentre study

    Howard, J. F., Utsugisawa, K., Benatar, M., Murai, H., Barohn, R. J., Illa, I., Jacob, S., Vissing, John, Burns, T. M., Kissel, J. T., Muppidi, S., Nowak, R. J., O'Brien, F., Wang, J., Mantegazza, R. & REGAIN Study Group, R. S. G., Dec 2017, In: Lancet Neurology. 16, 12, p. 976-986 11 p.

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

  6. Published

    Pure exercise intolerance and ophthalmoplegia associated with the m.12,294G > A mutation in the MT-TL2 gene: a case report

    Soldath, P., Madsen, K. L., Buch, A. E., Duno, M., Wibrand, F. & Vissing, John, Oct 2017, In: BMC Musculoskeletal Disorders. 18, 6 p., 419.

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

  7. 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

  8. Published

    Skeletal muscle metabolism during prolonged exercise in Pompe disease

    Preisler, N., Laforêt, P., Madsen, K. L., Husu, E., Vissing, C. R., Hedermann, G., Galbo, Henrik, Lindberg, C. & Vissing, John, Aug 2017, In: Endocrine Connections. 6, 6, p. 384-394 11 p.

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

  9. 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

  10. 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

  11. Published

    SCA28: Novel Mutation in the AFG3L2 Proteolytic Domain Causes a Mild Cerebellar Syndrome with Selective Type-1 Muscle Fiber Atrophy

    Svenstrup, K., Nielsen, T. T., Aidt, F., Rostgaard, N., Duno, M., Wibrand, F., Vinther-Jensen, T., Law, Ian, Vissing, John, Roos, P., Hjermind, L. E. & Nielsen, Jørgen Erik, Feb 2017, In: The Cerebellum. 16, 1, p. 62-67 6 p.

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

  12. Published

    Dysphagia is prevalent in patients with CPEO and single, large-scale deletions in mtDNA

    Pedersen, G. H., Løkken, N., Dahlqvist, J. R. & Vissing, John, Jan 2017, In: Mitochondrion. 32, p. 27-30 4 p.

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

  13. Published

    Effects of Sildenafil on Cerebrovascular Reactivity in Patients with Becker Muscular Dystrophy

    Lindberg, U., Witting, N., Jørgensen, S. L., Vissing, John, Rostrup, E., Larsson, Henrik Bo Wiberg & Kruuse, Christina Rostrup, Jan 2017, In: Neurotherapeutics. 14, 1, p. 182-190

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

  14. 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

  15. 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

  16. Published

    Aerobic anti-gravity exercise in patients with Charcot-Marie-Tooth disease types 1A and X: A pilot study

    Knak, K. L., Andersen, L. K. & Vissing, John, 2017, In: Brain and Behavior. 7, 12, 5 p., e00794.

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

  17. Published

    Aerobic training in myotonia congenita: Effect on myotonia and fitness

    Andersen, G., Løkken, N. & Vissing, John, 2017, In: Muscle and Nerve. 56, 4, p. 696-699 4 p.

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

  18. Published

    Fat Replacement of Paraspinal Muscles with Aging in Healthy Adults

    Dahlqvist, J. R., Vissing, C. R., Hedermann, G., Thomsen, C. & Vissing, John, 2017, In: Medicine and Science in Sports and Exercise. 49, 3, p. 595-601

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

  19. Published

    Glycogen synthesis in glycogenin 1-deficient patients: A role for glycogenin 2 in muscle

    Krag, T. O., Ruiz-Ruiz, C. & Vissing, John, 2017, In: Journal of Clinical Endocrinology and Metabolism. 102, 8, p. 2690-2700 11 p.

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

  20. Published

    High-intensity interval training in facioscapulohumeral muscular dystrophy type 1: a randomized clinical trial

    Andersen, G., Heje, K., Buch, A. E. & Vissing, John, 2017, In: Journal of Neurology. 264, 6, p. 1099-1106

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

  21. Published

    Human growth hormone stabilizes walking and improves strength in a patient with dominantly inherited calpainopathy

    Prahm, K. P., Feldt-Rasmussen, Ulla & Vissing, John, 2017, In: Neuromuscular Disorders. 27, 4, p. 358-362

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

  22. Published

    Impaired glycogen breakdown and synthesis in phosphoglucomutase 1 deficiency

    Preisler, N., Cohen, J., Vissing, C. R., Madsen, K. L., Heinicke, K., Sharp, L. J., Phillips, L., Romain, N., Park, S. Y., Newby, M., Wyrick, P., Mancias, P., Galbo, Henrik, Vissing, John & Haller, R. G., 2017, In: Molecular Genetics and Metabolism. 122, 3, p. 117-121

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

  23. Published

    Leber hereditary optic neuropathy due to a new ND1 mutation

    Soldath, P., Wegener, Marianne, Sander, B., Rosenberg, T., Duno, M., Wibrand, F. & Vissing, John, 2017, In: Ophthalmic Genetics. 38, 5, p. 480-485 6 p.

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

  24. Published

    MRI as outcome measure in facioscapulohumeral muscular dystrophy: 1-year follow-up of 45 patients

    Andersen, G., Dahlqvist, J. R., Vissing, C. R., Heje, K., Thomsen, C. & Vissing, John, 2017, In: Journal of Neurology. 264, 3, p. 438-447

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

  25. Published

    Mitochondrial Point Mutation m.3243A>G Associates With Lower Bone Mineral Density, Thinner Cortices, and Reduced Bone Strength: A Case-Control Study

    Langdahl, J. H., Frederiksen, A. L., Hansen, S. J., Andersen, P. H., Yderstraede, K. B., Dunø, M., Vissing, John & Frost, M., 2017, In: Journal of Bone and Mineral Research. 32, 10, p. 2041-2048

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

  26. 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

  27. Published

    Reliability of the 2- and 6-minute walk tests in neuromuscular diseases

    Knak, K. L., Andersen, L. K., Witting, N. & Vissing, John, 2017, In: Journal of Rehabilitation Medicine. 49, 4, p. 362-366 5 p.

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

  28. 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

  29. Published

    The antimyotonic effect of lamotrigine in non-dystrophic myotonias: a double-blind randomized study

    Andersen, G., Hedermann, G., Witting, N., Duno, M., Andersen, H. & Vissing, John, 2017, In: Brain. 140, 9, p. 2295-2305

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

  30. 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

  31. Published

    Update on new muscle glycogenosis

    Laforêt, P., Malfatti, E. & Vissing, John, 2017, In: Current Opinion in Neurology. 30, 5, p. 449-456

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

ID: 915367