John Vissing
Clinical Professor
- 2011
- Published
Clinical and molecular characterization of limb-girdle muscular dystrophy due to LAMA2 mutations
Gavassini, B. F., Carboni, N., Nielsen, Jørgen Erik, Danielsen, E. R., Thomsen, C., Svenstrup, K., Bello, L., Maioli, M. A., Marrosu, G., Ticca, A. F., Mura, M., Marrosu, M. G., Soraru, G., Angelini, C., Vissing, John & Pegoraro, E., Nov 2011, In: Muscle & Nerve. 44, 5, p. 703-9 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Clinical presentation and mutations in Danish patients with Wilson disease
Møller, L. B., Horn, N., Jeppesen, T. D., Vissing, John, Wibrand, F., Jennum, Poul & Ott, P., 2011, In: European Journal of Human Genetics. 19, 9, p. 935-41 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Deletion of exon 26 of the dystrophin gene is associated with a mild Becker muscular dystrophy phenotype
Witting, N., Duno, M. & Vissing, John, 2011, In: Acta Myologica. 30, 3, p. 182-4 3 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Deregulation of the ubiquitin-proteasome system is the predominant molecular pathology in OPMD animal models and patients
Anvar, S. Y., hoen, P. A., Venema, A., van der Sluijs, B., van Engelen, B., Snoeck, M., Vissing, John, Trollet, C., Dickson, G., Chartier, A., Simonelig, M., van Ommen, G. B., van der Maarel, S. M. & Raz, V., 2011, In: Skeletal Muscle. 1, 1, p. 15Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Level of muscle regeneration in limb-girdle muscular dystrophy type 2I relates to genotype and clinical severity
Krag, T. O., Hauerslev, S., Sveen, M. L., Schwartz, M. & Vissing, John, 2011, In: Skeletal Muscle. 1, 1, p. 31Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Physical training for McArdle disease
Quinlivan, R., Vissing, John, Hilton-Jones, D. & Buckley, J., 2011, In: Cochrane Database of Systematic Reviews. 12, p. CD007931Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Task force guidelines handbook: EFNS guidelines on diagnosis and management of fatty acid mitochondrial disorders.
Angelini, C., Federico, A., Reichmann, H., Lombes, A., Vianey-Saban, C., Chinnery, P., Turnbull, D. & Vissing, John, 2011, Task force guidelines handbook.: EFNS guidelines on diagnosis and management of fatty acid mitochondrial disorders.. 2 ed. Blackwell Publishing, Vol. 1. p. 501-511Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Research › peer-review
ID: 915367
Most downloads
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245
downloads
Skeletal muscle metabolism during prolonged exercise in Pompe disease
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
225
downloads
Reliability of the 2- and 6-minute walk tests in neuromuscular diseases
Research output: Contribution to journal › Letter › Research › peer-review
Published -
185
downloads
Aerobic Training in Patients with Congenital Myopathy
Research output: Contribution to journal › Journal article › Research › peer-review
Published