John Vissing

John Vissing

Clinical Professor

Member of:

  • Neurology


Publication year:
All
1 - 21 out of 21Page size: 25
  1. 2016
  2. Published

    Muscle involvement in limb-girdle muscular dystrophy with GMPPB deficiency (LGMD2T)

    Oestergaard, S. T., Stojkovic, T., Dahlqvist, J. R., Bouchet-Seraphin, C., Nectoux, J., Leturcq, F., Cossée, M., Solé, G., Thomsen, C., Krag, T. O. & Vissing, John, Dec 2016, In: Neurology: Genetics. 2, 6, 7 p., e112.

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

  3. 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

  4. 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

  5. Published

    Exercise training in metabolic myopathies

    Vissing, John, Oct 2016, In: Revue Neurologique. 172, 10, p. 559-565 7 p.

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

  6. Published

    Limb girdle muscular dystrophies: classification, clinical spectrum and emerging therapies

    Vissing, John, Oct 2016, In: Current Opinion in Neurology. 29, 5, p. 635-641 7 p.

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

  7. 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

  8. Published

    Differential glucose metabolism in mice and humans affected by McArdle disease

    Krag, T. O., Pinós, T., Nielsen, T. L., Duran, J., García-Rocha, M., Andreu, A. L. & Vissing, John, 1 Aug 2016, In: American Journal of Physiology: Regulatory, Integrative and Comparative Physiology. 311, 2, p. R307-R314

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

  9. Published

    Differential Muscle Involvement in Mice and Humans Affected by McArdle Disease

    Krag, T. O., Pinós, T., Nielsen, T. L., Brull, A., Andreu, A. L. & Vissing, John, May 2016, In: Journal of Neuropathology and Experimental Neurology. 75, 5, p. 441-54 14 p.

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

  10. 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

  11. Published

    Exercise Therapy in Spinobulbar Muscular Atrophy and Other Neuromuscular Disorders

    Dahlqvist, J. R. & Vissing, John, Mar 2016, In: Journal of Molecular Neuroscience. 58, 3, p. 388-93 6 p.

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

  12. Published

    Prevalence and phenotypes of congenital myopathy due to α-actin 1 gene mutations

    Witting, N., Werlauff, U., Duno, M. & Vissing, John, Mar 2016, In: Muscle & Nerve. 53, 3, p. 388-93 6 p.

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

  13. Published

    Towards a European Registry and Biorepository for Patients with Spinal and Bulbar Muscular Atrophy

    Pareyson, D., Fratta, P., Pradat, P., Soraru, G., Finsterer, J., Vissing, John, Jokela, M. E., Udd, B., Ludolph, A. C., Sagnelli, A. & Weydt, P., Mar 2016, In: Journal of Molecular Neuroscience. 58, 3, p. 394-400 7 p.

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

  14. Published

    Two- and 6-minute walk tests assess walking capability equally in neuromuscular diseases

    Andersen, L. K., Knak, K. L., Witting, N. & Vissing, John, 2 Feb 2016, In: Neurology. 86, 5, p. 442-5 4 p.

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

  15. Published

    Prevalence of migraine in persons with the 3243A>G mutation in mitochondrial DNA

    Guo, S., Esserlind, A., Andersson, Z., Frederiksen, A. L., Olesen, J., Vissing, John & dlt446, dlt446, Jan 2016, In: European Journal of Neurology. 23, 1, p. 175-81 7 p.

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

  16. Published

    Aerobic Training in Patients with Congenital Myopathy

    Hedermann, G., Vissing, C. R., Jensen, K., Preisler, N., Witting, N. & Vissing, John, 2016, In: PLoS ONE. 11, 1, 9 p., e0146036.

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

  17. Published

    Axial myopathy: an overlooked feature of muscle diseases

    Witting, N., Andersen, L. K. & Vissing, John, 2016, In: Brain. 139, 1, p. 13-22 10 p.

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

  18. Published

    Body weight-supported training in Becker and Limb Girdle 2I muscular dystrophy

    Jensen, B. R., Berthelsen, M. P., Husu, E., Christensen, S. B., Prahm, K. P. & Vissing, John, 2016, In: Muscle & Nerve. 54, 2, p. 239-243 5 p.

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

  19. Published

    Effect of Gender, Disease Duration and Treatment on Muscle Strength in Myasthenia Gravis

    Citirak, G., Cejvanovic, S., Andersen, H. & Vissing, John, 2016, In: PLOS ONE. 11, 10, p. 1-14 14 p., e0164092.

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

  20. Published

    Exercise Intolerance and Myoglobinuria Associated with a Novel Maternally Inherited MT-ND1 Mutation

    Rafiq, J., Duno, M., Østergaard, Elsebet, Ravn, K., Vissing, C. R., Wibrand, F. & Vissing, John, 2016, JIMD Reports. Springer, Vol. 25. p. 65-70 (JIMD Reports).

    Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Research › peer-review

  21. Published

    Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy

    Zaharieva, I. T., Thor, M. G., Oates, E. C., van Karnebeek, C., Hendson, G., Blom, E., Witting, N., Rasmussen, M., Gabbett, M. T., Ravenscroft, G., Sframeli, M., Suetterlin, K., Sarkozy, A., D'Argenzio, L., Hartley, L., Matthews, E., Pitt, M., Vissing, J., Ballegaard, M., Krarup, C. & 20 others, Slørdahl, A., Halvorsen, H., Ye, X. C., Zhang, L., Løkken, N., Werlauff, U., Abdelsayed, M., Davis, M. R., Feng, L., Phadke, R., Sewry, C. A., Morgan, J. E., Laing, N. G., Vallance, H., Ruben, P., Hanna, M. G., Lewis, S., Kamsteeg, E., Männikkö, R. & Muntoni, F., 2016, In: Brain. 139, 3, p. 674-91 18 p.

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

  22. Published

    Polymyositis following autologous haematopoietic stem cell transplantation

    Hedermann, G., Marquart, H. V. & Vissing, John, 2016, In: Scandinavian Journal of Rheumatology. 45, 5, p. 429-31 3 p.

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

ID: 915367